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PubChem aid: (prefix with "aid" like aid1431)
aidArticle TitleOrganizationDeposition
aid1159522 Identify HuR specific inhibitors 11762 11/09/16
aid1224863 Phenotypic Assay to Identify Small Molecules that Upregulate Production of hCFTR in HeLa Cells Southern Research Institute 11/09/16
aid1224899 mTOR Inhibition with eCF309 15254 11/09/16
aid1117296 Counterscreen for activators of Transthyretin (TTR) transcription: Luminescence-based cell-based high throughput dose response assay to identify inhibitors of Transthyretin (TTR) transcription in HuH7 hepatoma cells The Scripps Research Institute Molecular Screening Center 01/12/15
aid1117295 Fluorescence-based biochemical high throughput dose response assay to identify inhibitors of Trypanosoma brucei RNA editing ligase 1 (TbREL1). The Scripps Research Institute Molecular Screening Center 01/12/15
aid1117297 Luminescence-based cell-based high throughput dose response assay to identify activators of Transthyretin (TTR) transcription The Scripps Research Institute Molecular Screening Center 01/12/15
aid1053171 Counterscreen for inhibitors of LEDGF/p75-dependent integration: TR-FRET-based biochemical high throughput dose response counterscreen assay to identify activators of HIV-1 Integrase multimerization The Scripps Research Institute Molecular Screening Center 08/09/14
aid1053172 TR-FRET-based biochemical high throughput dose response assay to identify inhibitors of HIV-1 LEDGF/p75 DNA Integration The Scripps Research Institute Molecular Screening Center 08/09/14
aid743037 Counterscreen for agonists of the daf-12 abnormal Dauer Formation: Luminescence-based cell-based dose response assay to identify agonists of the Liver-X-Receptor (LXR). The Scripps Research Institute Molecular Screening Center 08/08/14
aid743052 Counterscreen for agonists of the daf-12 abnormal Dauer Formation: Luminescence-based cell-based dose response screening assay to identify agonists of the Liver-X-Receptor (LXR) The Scripps Research Institute Molecular Screening Center 08/08/14
aid720737 Counterscreen for agonists of the daf-12 abnormal Dauer Formation: Luminescence-based cell-based screening assay to identify agonists of the Liver-X-Receptor (LXR). The Scripps Research Institute Molecular Screening Center 08/08/14
aid743253 Counterscreen for exosite inhibitors of ADAM10: QFRET-based biochemical high throughput dose response assay to identify inhibitors of ADAM17 The Scripps Research Institute Molecular Screening Center 08/08/14
aid743259 Counterscreen for exosite inhibitors of ADAM17: Fluorescence resonance energy transfer (FRET)-based biochemical high throughput dose response assay to identify inhibitors of ADAM10 The Scripps Research Institute Molecular Screening Center 08/08/14
aid720547 Counterscreen for inhibitors of COUP-TFII (NR2F2): Luminescence-based cell-based high throughput dose response assay to identify inhibitors of the Herpes Virus Virion Protein 16 (VP16) The Scripps Research Institute Molecular Screening Center 08/08/14
aid743329 Counterscreen for inhibitors of phospholipase C isozymes (PLC-B3): Fluorescence-based biochemical high throughput dose response assay to identify inhibitors of phospholipase C isozymes (PLC-gamma1) The Scripps Research Institute Molecular Screening Center 08/08/14
aid720701 Dose Response confirmation of small molecule inhibitors originally identified via uHTS of Artemis endonuclease activity via a fluorescence intensity assay Burnham Center for Chemical Genomics 08/08/14
aid743297 Epi Absorbance-based biochemical high throughput dose response assay to identify inhibitors of human tyrosyl-DNA phosphodiesterase 2 (TDP2) The Scripps Research Institute Molecular Screening Center 08/08/14
aid720729 Fluorescence polarization-based biochemical high throughput dose response assay to identify inhibitors that disrupt the binding of a cyclic peptide (Tn6) to the fibrin proteolytic product D-Dimer and fragment E complex [DD(E )] The Scripps Research Institute Molecular Screening Center 08/08/14
aid720730 Fluorescence polarization-based biochemical high throughput dose response assay to identify inhibitors that disrupt the binding of a cyclic peptide (Tn7) to the fibrin proteolytic product D-Dimer and fragment E complex [DD(E )] The Scripps Research Institute Molecular Screening Center 08/08/14
aid743328 Fluorescence-based biochemical high throughput dose response assay to identify inhibitors of phospholipase C isozymes (PLC-B3) The Scripps Research Institute Molecular Screening Center 08/08/14
aid720638 Late stage Counterscreen for the probe development effort to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A): Luminescence-based cell-based high throughput dose response assay to identify agonists of the mu 1 opioid receptor (OPRM1) The Scripps Research Institute Molecular Screening Center 08/08/14
aid720639 Late stage for the probe development effort to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A): Luminescence-based cell-based high throughput dose response assay for agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) The Scripps Research Institute Molecular Screening Center 08/08/14
aid720734 Luminescence-based cell-based high throughput dose response assay to identify activators of the DAF-12 from the parasite S. stercoralis (ssDAF-12) The Scripps Research Institute Molecular Screening Center 08/08/14
aid743038 Luminescence-based cell-based high throughput dose response assay to identify agonists of the DAF-12 from the parasite H. contortus (hcDAF-12) The Scripps Research Institute Molecular Screening Center 08/08/14
aid743254 QFRET-based biochemical high throughput dose response assay to identify exosite inhibitors of ADAM10. The Scripps Research Institute Molecular Screening Center 08/08/14
aid743260 QFRET-based biochemical high throughput dose response assay to identify exosite inhibitors of ADAM17 The Scripps Research Institute Molecular Screening Center 08/08/14
aid743457 QFRET-based biochemical high throughput dose response assay to identify inhibitors of human group III secreted phospholipase A2 enzyme (HGIII-sPLA2) The Scripps Research Institute Molecular Screening Center 08/08/14
aid720645 TRFRET-based biochemical high throughput dose response assay to identify inhibitors of 5-meCpG-binding domain protein 2 (MBD2)-DBD binding to methylated oligonucleotide The Scripps Research Institute Molecular Screening Center 08/08/14
aid743453 TRFRET-based cell-based high throughput dose response assay to identify inhibitors of cell surface Prion Protein (PRPC) The Scripps Research Institute Molecular Screening Center 08/08/14
aid720500 Fluorescence Intensity-based biochemical primary high throughput dose response assay to identify activators of kallikrein-7 (K7) zymogen The Scripps Research Institute Molecular Screening Center 09/18/13
aid720521 Late stage assay provider counterscreen for TLR9 inhibitors: Luminescence-based assay to identify inhibitors of TLR9-dependent cell activation using RAW264.7 cells The Scripps Research Institute Molecular Screening Center 09/18/13
aid720548 Luminescence-based cell-based high throughput dose response assay to identify inhibitors of COUP-TFII (NR2F2) The Scripps Research Institute Molecular Screening Center 09/18/13
aid652151 Absorbance-based bacterial cell-based high throughput dose response assay to identify inhibitors of RecBCD The Scripps Research Institute Molecular Screening Center 06/21/13
aid651967 Absorbance-based biochemical high throughput dose response assay to identify inhibitors of Methionine sulfoxide reductase A (MsrA) The Scripps Research Institute Molecular Screening Center 06/21/13
aid652102 Confirmatory FRET assay using full length substrates for Botulinum neurotoxin light chain A protease, with Powder Set01 NMMLSC 06/21/13
aid686983 Counterscreen for agonists of the human trace amine associated receptor 1 (TAAR1): Fluorescence-based cell-based high throughput dose response assay to identify nonselective Ga16 agonists The Scripps Research Institute Molecular Screening Center 06/21/13
aid686988 Counterscreen for agonists of the human trace amine associated receptor 1 (TAAR1): Fluorescence-based cell-based high throughput dose response assay to identify nonselective Ga16 antagonists The Scripps Research Institute Molecular Screening Center 06/21/13
aid686984 Counterscreen for agonists of the human trace amine associated receptor 1 (hTAAR1): Fluorescence-based cell-based high throughput dose response assay to identify hTAAR1 agonist that also desensitize TAAR1 receptor response. The Scripps Research Institute Molecular Screening Center 06/21/13
aid686989 Counterscreen for antagonists of the human trace amine associated receptor 1 (TAAR1): Fluorescence-based cell-based high throughput dose reponse assay to identify nonselective Ga16 agonists The Scripps Research Institute Molecular Screening Center 06/21/13
aid686986 Counterscreen for antagonists of the human trace amine associated receptor 1 (hTAAR1): Fluorescence-based cell-based high throughput dose response assay to identify TAAR1 Agonists The Scripps Research Institute Molecular Screening Center 06/21/13
aid686987 Counterscreen for antagonists of the human trace amine associated receptor 1 (hTAAR1): Fluorescence-based cell-based high throughput dose response assay to identify nonselective Ga16 antagonists The Scripps Research Institute Molecular Screening Center 06/21/13
aid686958 Counterscreen for inhibitors of T-cell receptor (TCR)-CD3 interaction: Fluorescence-based biochemical high throughput dose response assay to identify inhibitors of T-cell receptor (TCR)-CD3 interaction using a TAMRA-labeled BSA probe The Scripps Research Institute Molecular Screening Center 06/21/13
aid687018 Counterscreen for inhibitors of the orphan nuclear receptor subfamily 0, group B, member 1 (DAX1; NR0B1): Luminescence-based cell-based high throughput dose response assay for nonselective inhibitors/assay artifacts using AP2 mutant SF-1 (NR5A1) Transactivation Assay The Scripps Research Institute Molecular Screening Center 06/21/13
aid651973 Counterscreen for inverse agonists of the liver receptor homolog-1 (LRH-1; NR5A2): Luminescence-based cell-based high throughput dose response assay to identify inhibitors of the Herpes Virus Virion Protein 16 (VP16) The Scripps Research Institute Molecular Screening Center 06/21/13
aid652002 Dose Response confirmation of uHTS hits for a small molecule Caspase-8 TRAIL sensitizers in a luminescence panel assay Burnham Center for Chemical Genomics 06/21/13
aid652006 Dose response confirmation of small molecule inhibitors of Low Molecular Weight Protein Tyrosine Phosphatase, LMPTP, in a fluorescence-based, Lymphoid Phosphatase (PTPN22, LYP-1) selectivity Assay Burnham Center for Chemical Genomics 06/21/13
aid652005 Dose response confirmation of small molecule inhibitors of Low Molecular Weight Protein Tyrosine Phosphatase, LMPTP, in an orthogonal absorbance-based assay Burnham Center for Chemical Genomics 06/21/13
aid652135 Fluorescence-based biochemical high throughput dose response assay for inhibitors of the fructose-bisphosphate aldolase (FBA) of M. tuberculosis The Scripps Research Institute Molecular Screening Center 06/21/13
aid686959 Fluorescence-based biochemical high throughput dose response assay to identify molecules that bind r(CAG) RNA repeats The Scripps Research Institute Molecular Screening Center 06/21/13
aid686957 Fluorescence-based biochemical primary high throughput dose response assay to identify inhibitors of T-cell receptor (TCR)-CD3 interaction using a TAMRA-labeled TCR probe The Scripps Research Institute Molecular Screening Center 06/21/13
aid686985 Fluorescence-based cell-based high throughput dose response assay to identify agonists of the human trace amine associated receptor 1 (TAAR1) The Scripps Research Institute Molecular Screening Center 06/21/13
aid686994 Fluorescence-based cell-based high throughput dose response assay to identify antagonists of the human trace amine associated receptor 1 (TAAR1) The Scripps Research Institute Molecular Screening Center 06/21/13
aid687013 Fluorescence-based cell-based primary high throughput dose response assay to identify antagonists of the Galanin Receptor 3 (GalR3). The Scripps Research Institute Molecular Screening Center 06/21/13
aid651971 Luminescence-based biochemical high throughput dose response assay for inhibitors of Trypanosoma brucei methionyl tRNA synthetase (MetRS) The Scripps Research Institute Molecular Screening Center 06/21/13
aid687017 Luminescence-based cell-based high throughput dose response assay for inhibitors of the orphan nuclear receptor subfamily 0, group B, member 1 (DAX1; NR0B1): repression of SF-1 (NR5A1) activated StAR promoter by full-length DAX-1 The Scripps Research Institute Molecular Screening Center 06/21/13
aid651970 Luminescence-based cell-based high throughput dose response assay for inverse agonists of the liver receptor homolog-1 (LRH-1; NR5A2) The Scripps Research Institute Molecular Screening Center 06/21/13
aid686991 Luminescence-based cell-based high throughput dose response assay to identify activators of the function of SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 2 (SMARCA2, BRM) The Scripps Research Institute Molecular Screening Center 06/21/13
aid686977 Vibrio cholerae assay for pro-quorum sensing small molecules Southern Research Specialized Biocontainment Screening Center 06/21/13
aid651728 Counter screen for HTS for Beta-2AR agonists with FAP-tagged human CCR5 with Powderset2 NMMLSC 06/20/13
aid651937 Counterscreen for discovery of small molecules that bind to the HIV-1-gp120 binding antibody, PG9 The Scripps Research Institute Molecular Screening Center 06/20/13
aid651939 Counterscreen for discovery of small molecules that bind to the HIV-1-gp120 binding antibody, PG9 The Scripps Research Institute Molecular Screening Center 06/20/13
aid651552 Counterscreen for inhibitors of the interaction of nucleotide-binding oligomerization domain containing 2 (NOD2) and receptor-interacting serine-threonine kinase 2 (RIPK2) The Scripps Research Institute Molecular Screening Center 06/20/13
aid651672 Counterscreen for inhibitors of the interaction of the lipase co-activator protein, abhydrolase domain containing 5 (ABHD5) with perilipin-5 (MLDP; PLIN5) The Scripps Research Institute Molecular Screening Center 06/20/13
aid651720 Counterscreen for inhibitors of the interaction of the lipase co-activator protein, abhydrolase domain containing 5 (ABHD5) with perilipin-5 (MLDP; PLIN5): Luminescence-based biochemical high throughput dose response assay to identify inhibitors of Hepatocyte nuclear factor 4 (HNF4) dimerization The Scripps Research Institute Molecular Screening Center 06/20/13
aid651579 Dose Response Confirmation of SKN-1 Inhibitor hits via a heat-shock counterscreen assay Burnham Center for Chemical Genomics 06/20/13
aid651650 Dose Response confirmation of small molecule modulators of the interaction between CendR and NRP-1 in a panel assay Burnham Center for Chemical Genomics 06/20/13
aid651639 Dose Response confirmation of uHTS hits for small molecule antagonists of the CRF-binding protein and CRF-R2 receptor complex in 384 well format Burnham Center for Chemical Genomics 06/20/13
aid651594 Dose Response counterscreen of small molecule antagonists of the CXCR6 receptor using a CXCR5 receptor luminescent beta-arrestin assay Burnham Center for Chemical Genomics 06/20/13
aid651563 Dose ResponseConfirmation of SKN-1 Inhibitor hits in a fluorescence ratio assay - Set 2 Burnham Center for Chemical Genomics 06/20/13
aid651684 Dose response confirmation of small molecule activators of alpha dystroglycan glycosylation Burnham Center for Chemical Genomics 06/20/13
aid651700 Dose response confirmation of small molecule inhibitors of Low Molecular Weight Protein Tyrosine Phosphatase, LMPTP, via a fluorescence intensity assay Burnham Center for Chemical Genomics 06/20/13
aid651693 Dose response confirmation of small molecule inhibitors of the catalytic domain of the SUMO protease, SENP1 in a FRET assay Burnham Center for Chemical Genomics 06/20/13
aid651697 Dose response confirmation of small molecule inhibitors of the catalytic domain of the SUMO protease, SENP1 in a kinetic FRET assay Burnham Center for Chemical Genomics 06/20/13
aid651581 Dose response confirmation of uHTS identification of HIF-2a Inhibitors in a luminesence assay Burnham Center for Chemical Genomics 06/20/13
aid651709 Dose response confirmation of uHTS inhibitor hits from NadD in a Colorimetric assay - Set 2 Burnham Center for Chemical Genomics 06/20/13
aid651570 Dose response validation of uHTS Gli-SUFU antagonist hits in a Wnt3a luminescent reporter assay Burnham Center for Chemical Genomics 06/20/13
aid651756 Dose responses of compounds that inhibit the Choline Transporter (CHT) in a 3H-choline uptake radioactive assay Johns Hopkins Ion Channel Center 06/20/13
aid651565 Dose-response confirmation of uHTS inhibitor hits of Sentrin-Specific Protease 8 in a Caspase-3 Fluorescence assay Burnham Center for Chemical Genomics 06/20/13
aid651559 Dose-response confirmation of uHTS inhibitor hits of Sentrin-Specific Protease 8 using a kinetic assay with Nedd8 Protein Substrate Burnham Center for Chemical Genomics 06/20/13
aid651680 Fluorescence polarization-based biochemical high throughput dose response assay for inhibitors of ArfGAP with SH3 domain, ankyrin repeat and PH domain 1 (ASAP1) The Scripps Research Institute Molecular Screening Center 06/20/13
aid651763 Fluorescence polarization-based biochemical high throughput dose response screening assay to identify inhibitors of ADP-ribosylation factor GTPase activating protein 1 (ARFGAP1) The Scripps Research Institute Molecular Screening Center 06/20/13
aid651553 Fluorescence-based cell-based high throughput dose response assay for inhibitors of the interaction of nucleotide-binding oligomerization domain containing 2 (NOD2) and the receptor-interacting serine-threonine kinase 2 (RIPK2) The Scripps Research Institute Molecular Screening Center 06/20/13
aid651677 Luminescence-based biochemical high throughput dose response assay for inhibitors of the interaction of the lipase co-activator protein, abhydrolase domain containing 5 (ABHD5) with perilipin-5 (MLDP; PLIN5) The Scripps Research Institute Molecular Screening Center 06/20/13
aid651733 Luminescence-based biochemical high throughput dose response assay for inhibitors of the interaction of the lipase co-activator protein, abhydrolase domain containing 5 (ABHD5) with perilipin-5 (MLDP; PLIN5) produced in HEK293T cells The Scripps Research Institute Molecular Screening Center 06/20/13
aid651675 SAR analysis of small molecule activators of alpha dystroglycan glycosylation Burnham Center for Chemical Genomics 06/20/13
aid651848 TRFRET-based biochemical high throughput dose response assay for small molecules that bind to the HIV-1-gp120 binding antibody, PG9 The Scripps Research Institute Molecular Screening Center 06/20/13
aid624241 Dose Response selectivity of inhibitors of STriatal-Enriched Phosphatase (STEP) in the Lymphoid Phosphatase (PTPN22) Inhibition Assay Burnham Center for Chemical Genomics 06/25/12
aid624207 Dose response orthogonal assay of uHTS small molecule inhibitors of Striatal-Enriched Phosphatase via a colorimetric intensity assay. Burnham Center for Chemical Genomics 06/25/12
aid624243 High-throughput multiplex microsphere dose response for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain A protease, compounds from Powder Set 01 NMMLSC 06/25/12
aid624245 High-throughput multiplex microsphere dose response for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain F protease, compounds from Powder Set 01 NMMLSC 06/25/12
aid624244 High-throughput multiplex microsphere dose response for inhibitors of toxin protease, specifically Lethal Factor protease, compounds from Powder Set 01 NMMLSC 06/25/12
aid623963 Absorbance-based biochemical high throughput dose response assay for activators of Methionine sulfoxide reductase A (MsrA) The Scripps Research Institute Molecular Screening Center 06/19/12
aid602264 Counterscreen for biased ligands (agonists) of the melanocortin 4 receptor (MC4R): Luminescence-based cell-based high throughput dose response assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors The Scripps Research Institute Molecular Screening Center 06/19/12
aid602234 Counterscreen for inhibitors of the Steroid Receptor Coactivator 1 (SRC1; NCOA1): Luminescence-based cell-based high throughput dose response assay to identify inhibitors of the Steroid Receptor Coactivator 3 (SRC3; NCOA3) The Scripps Research Institute Molecular Screening Center 06/19/12
aid623996 Dose Response HTS singleplex for inhibitors of yeast efflux pump, specifically Cdr1 with Cherry Pick2 compound set NMMLSC 06/19/12
aid623994 Dose Response HTS singleplex for inhibitors of yeast efflux pump, specifically Cdr2 with Cherry Pick2 compound set NMMLSC 06/19/12
aid623992 Dose Response HTS singleplex for inhibitors of yeast efflux pump, specifically Mdr1 with Cherry Pick2 compound set NMMLSC 06/19/12
aid602473 Dose Response confirmation of uHTS hits for small molecule agonists of the CRF-binding protein and CRF-R2 receptor complex Burnham Center for Chemical Genomics 06/19/12
aid623955 Dose Response of Flow Cytometric HTS Screen for inhibitors of the ABC transporter ABCB6 for Cherry Pick01 NMMLSC 06/19/12
aid602257 Dose Response of Small Molecules that Regulate V-ATPase Proton Transport in Yeast using pHLuorin, Powder Set1 NMMLSC 06/19/12
aid602374 Dose Response selectivity of inhibitors of STriatal-Enriched Phosphatase (STEP) in the dual-specificity protein-tyrosine phosphatase VHR Inhibition Assay Burnham Center for Chemical Genomics 06/19/12
aid602367 Dose Response selectivity of inhibitors of Striatal-Enriched Phosphatase (STEP) in a SHP2 (PTPN11) Inhibition Assay Burnham Center for Chemical Genomics 06/19/12
aid602369 Dose Response validation of uHTS RPN11 inhibitor hits using a Thrombin Fluorescence Polarization assay Burnham Center for Chemical Genomics 06/19/12
aid602304 Dose Response with BCECF Assay for V-ATPase inhibitors that increase vacuolar pH, Powder Set 1 NMMLSC 06/19/12
aid602386 Dose response confirmation of DNMT1 inhibitors in a Fluorescent Molecular Beacon assay Burnham Center for Chemical Genomics 06/19/12
aid602368 Dose response confirmation of uHTS RPN11 inhibitor hits in a Fluorescence Polarization assay Burnham Center for Chemical Genomics 06/19/12
aid602464 Dose response confirmation of uHTS antagonist hits from Gli-SUFU in a luminescent reporter assay Burnham Center for Chemical Genomics 06/19/12
aid602372 Dose response confirmation of uHTS small molecule inhibitors of Striatal-Enriched Phosphatase via a fluorescence intensity assay Burnham Center for Chemical Genomics 06/19/12
aid623882 Dose response for HTS for Beta-2AR agonists via FAP method from Powderset2 NMMLSC 06/19/12
aid623947 Dose response for HTS for Beta-2AR agonists via FAP method from Powderset3 NMMLSC 06/19/12
aid602376 Dose responses of compounds that activate the Choline Transporter (CHT) - 10 point CRC Johns Hopkins Ion Channel Center 06/19/12
aid602259 Dose-response confirmation of microRNA-mediated mRNA deadenylation inhibitors by fluoresence polarization assay Burnham Center for Chemical Genomics 06/19/12
aid602260 Dose-response secondary confirmation of microRNA-mediated mRNA deadenylation inhibitors by fluoresence polarization assay using Cy5 labeled peptide Burnham Center for Chemical Genomics 06/19/12
aid602328 High-throughput multiplex microsphere dose response for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain A protease, compounds from Cherry Pick 02 NMMLSC 06/19/12
aid602338 High-throughput multiplex microsphere dose response for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain F protease, compounds from Cherry Pick 02 NMMLSC 06/19/12
aid602326 High-throughput multiplex microsphere dose response for inhibitors of toxin protease, specifically Lethal Factor protease, compounds from Cherry Pick 02 NMMLSC 06/19/12
aid602263 Luminescence-based cell-based high throughput dose response assay for biased ligands (agonists) of the melanocortin 4 receptor (MC4R) The Scripps Research Institute Molecular Screening Center 06/19/12
aid602235 Luminescence-based cell-based high throughput dose response assay for inhibitors of the Steroid Receptor Coactivator 1 (SRC1; NCOA1) The Scripps Research Institute Molecular Screening Center 06/19/12
aid602469 SAR analysis of small molecule Activators of Apaf-1 in a Fluorescent assay - set 2 Burnham Center for Chemical Genomics 06/19/12
aid602460 SAR analysis of small molecule Inhibitors of Apaf-1 in a Fluorescent assay - set 2 Burnham Center for Chemical Genomics 06/19/12
aid602471 SAR analysis of small molecule activators of Apaf-1 using a LZ-Caspase-9/Caspase-3 Fluorescent Selectivity assay - Set 2 Burnham Center for Chemical Genomics 06/19/12
aid624089 SAR analysis of small molecule inhibitors of APOBEC3A DNA Deaminase via a fluorescence-based single-stranded DNA deaminase assay - Set 2 Burnham Center for Chemical Genomics 06/19/12
aid624087 SAR analysis of small molecule inhibitors of APOBEC3G DNA Deaminase via a fluorescence-based single-stranded DNA deaminase assay - Set 2 Burnham Center for Chemical Genomics 06/19/12
aid602461 SAR analysis of small molecule inhibitors of Apaf-1 using a LZ-Caspase-9/Caspase-3 Fluorescent Selectivity assay - Set 2 Burnham Center for Chemical Genomics 06/19/12
aid602375 SAR analysis of small molecule inhibitors of tim23-1 yeast via a luminescent assay Burnham Center for Chemical Genomics 06/19/12
aid602380 SAR analysis of small molecule inhibitors of tim23-1: a luminescent TIM10 yeast counterscreen. Burnham Center for Chemical Genomics 06/19/12
aid602378 SAR analysis of small molecule inhibitors of tim23-1: a luminescent tim10-1 yeast counterscreen. Burnham Center for Chemical Genomics 06/19/12
aid602298 TRFRET-based cell-based high throughput dose response assay for biased ligands (antagonists) of the melanocortin 4 receptor (MC4R) The Scripps Research Institute Molecular Screening Center 06/19/12
aid602151 Cellular PLD1 concentration response Vanderbilt Specialized Chemistry Center 06/18/12
aid602147 Cellular PLD2 concentration response Vanderbilt Specialized Chemistry Center 06/18/12
aid602167 Counterscreen for inhibitors of the Steroid Receptor Coactivator 3 (SRC3; NCOA3): Luminescence-based cell-based high throughput dose response assay to identify inhibitors of the Herpes Virus Virion Protein 16 (VP16) The Scripps Research Institute Molecular Screening Center 06/18/12
aid602168 Counterscreen for inhibitors of the Steroid Receptor Coactivator 3 (SRC3; NCOA3): Luminescence-based cell-based high throughput dose response assay to identify inhibitors of the Steroid Receptor Coactivator 1 (SRC1; NCOA1) The Scripps Research Institute Molecular Screening Center 06/18/12
aid602198 Dose Response of Small Molecules that Regulate V-ATPase Proton Transport in Yeast using pHLuorin, Cherry Pick 2 NMMLSC 06/18/12
aid602176 High-throughput multiplex microsphere dose response for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain A protease, compounds from Cherry Pick 01 NMMLSC 06/18/12
aid602177 High-throughput multiplex microsphere dose response for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain F protease, compounds from Cherry Pick 01 NMMLSC 06/18/12
aid602178 High-throughput multiplex microsphere dose response for inhibitors of toxin protease, specifically Lethal Factor protease, compounds from Cherry Pick 01 NMMLSC 06/18/12
aid602208 JHICC_CHT_Inh_3H uptake_CRC Johns Hopkins Ion Channel Center 06/18/12
aid602166 Luminescence-based cell-based high throughput dose response assay for inhibitors of the Steroid Receptor Coactivator 3 (SRC3; NCOA3) The Scripps Research Institute Molecular Screening Center 06/18/12
aid602150 PLD1 purified enzyme concentration response Vanderbilt Specialized Chemistry Center 06/18/12
aid602149 PLD2 purified enzyme concentration response Vanderbilt Specialized Chemistry Center 06/18/12
aid602136 SAR analysis of small molecule inhibitors of APOBEC3G DNA Deaminase via a fluorescence-based single-stranded DNA deaminase assay Burnham Center for Chemical Genomics 06/18/12
aid602181 TRFRET-based biochemical high throughput dose response assay for inhibitors of the interaction of the Ras and Rab interactor 1 protein (Rin1) and the c-abl oncogene 1, non-receptor tyrosine kinase (Abl) The Scripps Research Institute Molecular Screening Center 06/18/12
aid588783 Dose Response Assay for Inhibitors of the beta-Arrestin-Adaptor Protein 2 Interaction for Cherry Pick 1 NMMLSC 01/06/12
aid588606 Dose Response HTS singleplex for inhibitors of yeast efflux pump, specifically Cdr1 with Hit compounds from Cherry Pick1 NMMLSC 01/06/12
aid588604 Dose Response HTS singleplex for inhibitors of yeast efflux pump, specifically Cdr2 with Hit compounds from Cherry Pick1 NMMLSC 01/06/12
aid588608 Dose Response HTS singleplex for inhibitors of yeast efflux pump, specifically Mdr1 with Hit compounds from Cherry Pick1 NMMLSC 01/06/12
aid588554 Dose Response confirmation of uHTS Activators of the Apaf-1 Pathway in Fluorescent format Burnham Center for Chemical Genomics 01/06/12
aid588596 Dose Response of Small Molecules that Regulate V-ATPase Proton Transport in Yeast using pHLuorin, Cherry Pick 1 NMMLSC 01/06/12
aid588592 Dose Response validation of Activators of Apaf-1 using a Fluorescent Interference Counterscreen assay Burnham Center for Chemical Genomics 01/06/12
aid588637 Dose response assay for compounds that inhibit KCNQ2 potassium channels on automated electrophysiological assay II Johns Hopkins Ion Channel Center 01/06/12
aid588584 Dose response confirmation of the uHTS fluorescent assay for identification of inhibitors of ATG4B Set 2 Burnham Center for Chemical Genomics 01/06/12
aid588574 Dose response confirmation of uHTS hits for Apaf-1 using a LZ-Caspase-9/Caspase-3 Fluorescent Selectivity assay Burnham Center for Chemical Genomics 01/06/12
aid588586 Dose response counterscreen of uHTS hits for ATG4B inhibitors in a Phospholipase A2 assay Set 2 Burnham Center for Chemical Genomics 01/06/12
aid588763 Dose response for HTS for Beta-2AR agonists via FAP method from CP1 NMMLSC 01/06/12
aid588775 Dose response for HTS for Beta-2AR agonists via FAP method from Powderset1 NMMLSC 01/06/12
aid588769 Late stage assay provider results from the probe development effort to identify inhibitors of plasma platelet activating factor acetylhydrolase (pPAFAH): fluorescence-based dose response biochemical gel-based competitive Activity-Based Protein Profiling (ABPP) assay for HTS compounds The Scripps Research Institute Molecular Screening Center 01/06/12
aid588601 SAR Analysis of small molecule inhibitors of Sentrin-specific protease 8 (SENP8) using a Luminescent assay - Set 2 Burnham Center for Chemical Genomics 01/06/12
aid588603 SAR analysis of small molecule activators of the MazEF TA System via a fluorescence-based single-stranded RNase assay Burnham Center for Chemical Genomics 01/06/12
aid588411 Counterscreen for agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors: Luminescence-based cell-based high throughput dose response assay to identify agonists of OPRD1 homodimerization The Scripps Research Institute Molecular Screening Center 01/05/12
aid588538 Dose Response validation of Inhibitors of Apaf-1 using a Fluorescent Interference Counterscreen assay Burnham Center for Chemical Genomics 01/05/12
aid588524 Dose response confirmation of uHTS hits for Apaf-1 in a Fluorescent assay Burnham Center for Chemical Genomics 01/05/12
aid588481 Dose response confirmation uHTS hits for MazEF TA System activators via a fluorescence-based single-stranded RNase assay Burnham Center for Chemical Genomics 01/05/12
aid588502 Dose response confirmation uHTS hits for MazEF TA System activators via a fluorescence-based single-stranded RNase assay counterscreen Burnham Center for Chemical Genomics 01/05/12
aid588400 Dose response counterscreen of uHTS hits for ATG4B inhibitors in a Phospholipase A2 assay Burnham Center for Chemical Genomics 01/05/12
aid588504 Luminescence-based cell-based high throughput dose response assay for activators of the GAA850 frataxin (FXN) promoter The Scripps Research Institute Molecular Screening Center 01/05/12
aid588359 SAR analysis counterscreen of small molecule antagonists of the CCR6 receptor using an APJ receptor luminescent beta-arrestin assay Burnham Center for Chemical Genomics 01/05/12
aid588341 Counterscreen for inhibitors of TLR9-MyD88 binding: fluorescence-based cell-based high throughput dose response assay to identify non-selective inhibitors of the beta-lactamase enzyme (BLA) The Scripps Research Institute Molecular Screening Center 01/04/12
aid540297 Dose Response confirmation of uHTS hits for Scp-1 phosphatase using a colorimetric assay Burnham Center for Chemical Genomics 01/04/12
aid540252 Dose Response orthogonal assay utilizing the direct end-point detection of NADPH for uHTS small molecule inhibitors of Plasmodium falciparum Glucose-6-phosphate dehydrogenase Burnham Center for Chemical Genomics 01/04/12
aid540269 Dose Response orthogonal kinetic assay utilizing the direct detection of NADPH for uHTS small molecule inhibitors of Plasmodium falciparum Glucose-6-phosphate dehydrogenase Burnham Center for Chemical Genomics 01/04/12
aid588340 Fluorescence-based cell-based high throughput dose response assay for inhibitors of TLR9-MyD88 binding The Scripps Research Institute Molecular Screening Center 01/04/12
aid540288 SAR VHR1 Fluorescent Assay for In Vitro dose response studies Set 3 Burnham Center for Chemical Genomics 01/04/12
aid540334 SAR analysis of small molecule antagonists of the CCR6 receptor: a luminescent beta-arrestin assay Burnham Center for Chemical Genomics 01/04/12
aid504893 Counterscreen for activators of the Protein Kinase A-R1A (PKA-R1A) complex: fluorescence polarization-based biochemical high throughput dose response assay to identify activators of the Protein Kinase A-R2B (PKA-R2B) complex The Scripps Research Institute Molecular Screening Center 08/04/11
aid504896 Counterscreen for activators of the Protein Kinase A-R2B (PKA-R2B) complex: fluorescence polarization-based biochemical high throughput dose response assay to identify activators of the Protein Kinase A-R1A (PKA-R1A) complex The Scripps Research Institute Molecular Screening Center 08/04/11
aid504762 Dose Response confirmation of activators of hexokinase domain containing I (HKDC1) in the hexokinase 1 selectivity assay Burnham Center for Chemical Genomics 08/04/11
aid504763 Dose Response confirmation of inhibitors of hexokinase domain containing I (HKDC1) in the hexokinase 1 selectivity assay Burnham Center for Chemical Genomics 08/04/11
aid504765 Dose Response confirmation of uHTS small molecule inhibitors of Plasmodium falciparum Glucose-6-phosphate dehydrogenase via a fluorescence intensity assay Burnham Center for Chemical Genomics 08/04/11
aid504887 Fluorescence polarization-based biochemical high throughput dose response assay for activators of the Protein Kinase A-R1A (PKA-R1A) complex The Scripps Research Institute Molecular Screening Center 08/04/11
aid504888 Fluorescence polarization-based biochemical high throughput dose response assay for activators of the Protein Kinase A-R2B (PKA-R2B) complex The Scripps Research Institute Molecular Screening Center 08/04/11
aid504792 Human Glucose-6-Phosphate Dehydrogenase Dose Response Selectivity Assay for Inhibitors of Plasmodium falciparum Glucose-6-Phosphate Dehydrogenase Burnham Center for Chemical Genomics 08/04/11
aid504723 Dose Response confirmation of APOBEC3A DNA Deaminase Inhibitors via a A3G counterscreen Burnham Center for Chemical Genomics 08/03/11
aid504722 Dose Response confirmation of APOBEC3G DNA Deaminase Inhibitors via a A3A counterscreen Burnham Center for Chemical Genomics 08/03/11
aid504549 Dose Response confirmation of Image-Based HTS for Selective Agonists for NTR1 Burnham Center for Chemical Genomics 08/03/11
aid504593 Dose Response confirmation of Inhibitors of Mdm2/MdmX interaction in luminescent format Burnham Center for Chemical Genomics 08/03/11
aid504669 Dose Response confirmation of Inhibitors of Mdm2/MdmX interaction using a Brca1/Bard1 BiLC Counterscreen assay Burnham Center for Chemical Genomics 08/03/11
aid504689 Dose Response confirmation of UBC13 Polyubiquitin Inhibitors using a Bfl-1 counterscreen Burnham Center for Chemical Genomics 08/03/11
aid504730 Dose Response confirmation of activators of hexokinase domain containing I (HKDC1) Burnham Center for Chemical Genomics 08/03/11
aid504729 Dose Response confirmation of inhibitors of hexokinase domain containing I (HKDC1) Burnham Center for Chemical Genomics 08/03/11
aid504724 Dose Response confirmation of small molecule APOBEC3A DNA Deaminase Inhibitors via a fluorescence-based single-stranded DNA deaminase assay Burnham Center for Chemical Genomics 08/03/11
aid504719 Dose Response confirmation of small molecule APOBEC3G DNA Deaminase Inhibitors via a fluorescence-based single-stranded DNA deaminase assay Burnham Center for Chemical Genomics 08/03/11
aid504728 Dose Response confirmation of small molecule antagonists of the CCR6 receptor: a luminescent beta-arrestin assay Burnham Center for Chemical Genomics 08/03/11
aid504544 Dose Response confirmation of uHTS small molecule inhibitors of tim10-1: a luminescent tim23-1 yeast counterscreen. Burnham Center for Chemical Genomics 08/03/11
aid504672 Dose Response confirmation of uHTS small molecule inhibitors of tim23-1: a luminescent TIM10 yeast counterscreen. Burnham Center for Chemical Genomics 08/03/11
aid504657 Dose Response confirmation of uHTS small molecule inhibitors of tim23-1: a luminescent tim10-1 yeast counterscreen. Burnham Center for Chemical Genomics 08/03/11
aid504565 Dose Response of Developing T Cell Immune Modulators with powder sourced compounds NMMLSC 08/03/11
aid504500 Dose Response of inhibitors of GRK2 binding with RNA aptamer, Cherry Pick 1 NMMLSC 08/03/11
aid504330 Dose response assay for dual activators of procaspase-3 and procaspase-7: Absorbance-based biochemical high throughput screening assay to identify activators of procaspase-7 The Scripps Research Institute Molecular Screening Center 08/03/11
aid504756 Dose response confirmation of the uHTS fluorescent assay for identification of inhibitors of ATG4B. Burnham Center for Chemical Genomics 08/03/11
aid504328 Dose response counterscreen for dual activators of procaspase-3 and procaspase-7: Absorbance-based biochemical high throughput screening assay to identify activators of procaspase-3 The Scripps Research Institute Molecular Screening Center 08/03/11
aid504698 Fluorescence-based biochemical high throughput dose response assay for activators of the calcium sensitivity of cardiac Regulated Thin Filaments (RTF) The Scripps Research Institute Molecular Screening Center 08/03/11
aid504742 Fluorescence-based biochemical high throughput dose response assay for inhibitors of the calcium sensitivity of cardiac Regulated Thin Filaments (RTF) The Scripps Research Institute Molecular Screening Center 08/03/11
aid504699 Fluorescence-based cell-based high throughput dose response assay for antagonists of the orexin 1 receptor (OX1R; HCRTR1) The Scripps Research Institute Molecular Screening Center 08/03/11
aid504453 Fluorescence-polarization-based biochemical polarscreen dose response binding assay for partial agonists of the peroxisome proliferator-activated receptor gamma (PPARg) The Scripps Research Institute Molecular Screening Center 08/03/11
aid504712 HTS Dose response counterscreen for assays utilizing the enzyme, beta-galactosidase - Set 3 Burnham Center for Chemical Genomics 08/03/11
aid504701 Homogeneous Time Resolved Fluorescence (HTRF)-based cell-based high throughput dose response assay for antagonists of the orexin 1 receptor (OX1R; HCRTR1) The Scripps Research Institute Molecular Screening Center 08/03/11
aid504735 Late stage assay provider counterscreen for partial agonists of the peroxisome proliferator-activated receptor gamma (PPARg): Luminescence-based cell-based dose response assay for partial agonists of the peroxisome proliferator-activated receptor alpha (PPARA). The Scripps Research Institute Molecular Screening Center 08/03/11
aid504460 Late-stage fluorescence dose response cell-based assay to identify agonists of the Sphingosine 1-Phosphate Receptor 4 (S1P4): purchased compounds EC50 The Scripps Research Institute Molecular Screening Center 08/03/11
aid504410 Late-stage radioligand binding dose response assay to identify inhibitors of NADPH oxidase 1 (NOX1): PDSP screen Ki Set 2 The Scripps Research Institute Molecular Screening Center 08/03/11
aid504447 Luminescence-based cell-based assay provider high throughput dose response assay for partial agonists of the peroxisome proliferator-activated receptor gamma (PPARg) The Scripps Research Institute Molecular Screening Center 08/03/11
aid504589 SAR Analysis for the identification of selective inhibits of the transient receptor potential cation channel C4 (TRPC4): Automated Electrophysiology_2 Johns Hopkins Ion Channel Center 08/03/11
aid504446 TR-FRET-based biochemical dose response competitive binding lanthascreen assay for partial agonists of the peroxisome proliferator-activated receptor gamma (PPARg) The Scripps Research Institute Molecular Screening Center 08/03/11
aid489014 Absorbance-based biochemical high throughput dose response assay for activators of procaspase-3 The Scripps Research Institute Molecular Screening Center 08/02/11
aid504322 CHOP dose-response primary assay Emory University Molecular Libraries Screening Center 08/02/11
aid492957 Counterscreen for AddAB inhibitors: absorbance-based bacterial cell-based high throughput dose response assay to identify inhibitors of RecBCD The Scripps Research Institute Molecular Screening Center 08/02/11
aid489013 Counterscreen for procaspase-3 activators: absorbance-based biochemical high throughput dose response assay for activators of procaspase-7 The Scripps Research Institute Molecular Screening Center 08/02/11
aid493155 Dose Response confirmation of uHTS for the identification of UBC13 Polyubiquitin Inhibitors via a TR-FRET Assay Burnham Center for Chemical Genomics 08/02/11
aid493182 Dose Response confirmation of uHTS for the identification of UBC13 Polyubiquitin Inhibitors via a TR-FRET Assay reconfirm Burnham Center for Chemical Genomics 08/02/11
aid493003 Dose Response confirmation of uHTS small molecule inhibitors of tim10-1 yeast via a luminescent assay Burnham Center for Chemical Genomics 08/02/11
aid492970 Fluorescence-based biochemical dose response assay to identify inhibitors of Protein Arginine Deiminase 4 (PAD4) The Scripps Research Institute Molecular Screening Center 08/02/11
aid493021 Inhibitors of T-Type Calcium Channels Vanderbilt Screening Center for GPCRs, Ion Channels and Transporters 08/02/11
aid493022 Inhibitors of T-Type Calcium Channels (SynthLib1) Vanderbilt Screening Center for GPCRs, Ion Channels and Transporters 08/02/11
aid493023 Inhibitors of T-Type Calcium Channels (SynthLib2) Vanderbilt Screening Center for GPCRs, Ion Channels and Transporters 08/02/11
aid489010 Intein inhibitors as potential Tuberculosis drugs Southern Research Specialized Biocontainment Screening Center 08/02/11
aid504317 Luminescence-based biochemical high throughput dose response assay for inhibitors of the interaction of the lipase co-activator protein, abhydrolase domain containing 5 (ABHD5) with perilipin-1 (PLIN1) (2K validation set) The Scripps Research Institute Molecular Screening Center 08/02/11
aid504319 Luminescence-based biochemical high throughput dose response assay for inhibitors of the interaction of the lipase co-activator protein, abhydrolase domain containing 5 (ABHD5) with perilipin-5 (MLDP; PLIN5) (2K validation set) The Scripps Research Institute Molecular Screening Center 08/02/11
aid492991 SAR Analysis for the identification of selective inhibits of the transient receptor potential cation channel C4 (TRPC4): Automated Electrophysiology Johns Hopkins Ion Channel Center 08/02/11
aid504313 XBP1 DR counterscreen for CHOP Emory University Molecular Libraries Screening Center 08/02/11
aid485288 A confirmatory biochemical assay using the ADP-Hunter methodology, purified TAg, and ATP to quantify activity of synthesized compounds that inhibit the ATPase activity of Tag (3) Southern Research Specialized Biocontainment Screening Center 08/01/11
aid488790 Confirmatory Cherry Pick 3 SAR Dose Response Multiplex in TOR pathway GFP-fusion proteins for Saccharomyes cerevisiae, specifically AGP1 NMMLSC 08/01/11
aid488825 Confirmatory Cherry Pick 3 SAR Dose Response Multiplex in TOR pathway GFP-fusion proteins for Saccharomyes cerevisiae, specifically CIT2 NMMLSC 08/01/11
aid488823 Confirmatory Cherry Pick 3 SAR Dose Response Multiplex in TOR pathway GFP-fusion proteins for Saccharomyes cerevisiae, specifically LAP4 NMMLSC 08/01/11
aid488812 Confirmatory Cherry Pick 3 SAR Dose Response Multiplex in TOR pathway GFP-fusion proteins for Saccharomyes cerevisiae, specifically MEP2 NMMLSC 08/01/11
aid488814 Confirmatory Cherry Pick 3 SAR Dose Response Multiplex in TOR pathway GFP-fusion proteins for Saccharomyes cerevisiae, specifically RPL19A NMMLSC 08/01/11
aid463257 Counterscreen for NR2E3 inverse agonists: TR-FRET-based biochemical high throughput dose response assay to identify inverse agonists of the interaction between peroxisome proliferator-activated receptor gamma (PPARg) and nuclear receptor co-repressor 2 (NCOR2) The Scripps Research Institute Molecular Screening Center 08/01/11
aid488861 Dose Response Confirmation of compounds that inhibit VHR1 in Fluorescent Assay Burnham Center for Chemical Genomics 08/01/11
aid488817 Dose Response concentration confirmation of uHTS hits from a small molecule activators of human intestinal alkaline phosphatase via a luminescent assay - Set 2 Burnham Center for Chemical Genomics 08/01/11
aid488783 Dose Response concentration confirmation of uHTS hits from a small molecule activators of mouse intestinal alkaline phosphatase via a luminescent assay Burnham Center for Chemical Genomics 08/01/11
aid488923 Dose Response confirmation of compounds that inhibit HePTP Burnham Center for Chemical Genomics 08/01/11
aid488863 Dose Response confirmation of inhibitors of NALP1 in yeast using a Caspase-1-ASC counter screen. Burnham Center for Chemical Genomics 08/01/11
aid488800 Dose Response confirmation of inhibitors of NALP3 in yeast using a Caspase-1-ASC counter screen Burnham Center for Chemical Genomics 08/01/11
aid488901 Dose Response confirmation of inhibitors of Sentrin-specific proteases (SENPs) using a Caspase-3 Selectivity assay Burnham Center for Chemical Genomics 08/01/11
aid488920 Dose Response confirmation of inhibitors of Sentrin-specific proteases (SENPs) using a Luminescent Interference Counterscreen assay Burnham Center for Chemical Genomics 08/01/11
aid488875 Dose Response confirmation of uHTS activators of Human Intestinal Alkaline Phosphatase using Mouse Intestinal Alkaline Phosphatase Burnham Center for Chemical Genomics 08/01/11
aid488888 Dose Response confirmation of uHTS activators of Human Intestinal Alkaline Phosphatase using Placental Alkaline Phosphatase Burnham Center for Chemical Genomics 08/01/11
aid488886 Dose Response confirmation of uHTS activators of Human Intestinal Alkaline Phosphatase using Tissue Nonspecific Alkaline Phosphatase. Burnham Center for Chemical Genomics 08/01/11
aid488873 Dose Response confirmation of uHTS activators of Mouse Intestinal Alkaline Phosphatase using Human Intestinal Alkaline Phosphatase Burnham Center for Chemical Genomics 08/01/11
aid488878 Dose Response confirmation of uHTS activators of Mouse Intestinal Alkaline Phosphatase using Placental Alkaline Phosphatase Burnham Center for Chemical Genomics 08/01/11
aid488880 Dose Response confirmation of uHTS activators of Mouse Intestinal Alkaline Phosphatase using Tissue Nonspecific Alkaline Phosphatase. Burnham Center for Chemical Genomics 08/01/11
aid488921 Dose Response confirmation of uHTS for inhibitors of Sentrin-specific protease 6 (SENP6) using a Luminescent assay Burnham Center for Chemical Genomics 08/01/11
aid488903 Dose Response confirmation of uHTS for inhibitors of Sentrin-specific protease 8 (SENP8) using a Luminescent assay Burnham Center for Chemical Genomics 08/01/11
aid488860 Dose Response confirmation of uHTS for the identification of inhibitors of NALP1 in yeast using a luminescent assay Burnham Center for Chemical Genomics 08/01/11
aid488799 Dose Response confirmation of uHTS for the identification of inhibitors of NALP3 in yeast using a luminescent assay Burnham Center for Chemical Genomics 08/01/11
aid488748 Dose Response confirmation of uHTS hits from a small molecule agonists of the APJ receptor via a luminescent beta-arrestin assay Burnham Center for Chemical Genomics 08/01/11
aid488793 Dose Response confirmation of uHTS hits from a small molecule inhibitors of human intestinal alkaline phosphatase via a luminescent assay - Set 2 Burnham Center for Chemical Genomics 08/01/11
aid488785 Dose Response confirmation of uHTS hits from a small molecule inhibitors of mouse intestinal alkaline phosphatase via a luminescent assay Burnham Center for Chemical Genomics 08/01/11
aid488874 Dose Response confirmation of uHTS inhibitors of Human Intestinal Alkaline Phosphatase using Mouse Intestinal Alkaline Phosphatase Burnham Center for Chemical Genomics 08/01/11
aid488892 Dose Response confirmation of uHTS inhibitors of Human Intestinal Alkaline Phosphatase using Placental Alkaline Phosphatase Burnham Center for Chemical Genomics 08/01/11
aid488882 Dose Response confirmation of uHTS inhibitors of Human Intestinal Alkaline Phosphatase using Tissue Nonspecific Alkaline Phosphatase. Burnham Center for Chemical Genomics 08/01/11
aid488876 Dose Response confirmation of uHTS inhibitors of Mouse Intestinal Alkaline Phosphatase using Human Intestinal Alkaline Phosphatase Burnham Center for Chemical Genomics 08/01/11
aid488879 Dose Response confirmation of uHTS inhibitors of Mouse Intestinal Alkaline Phosphatase using Placental Alkaline Phosphatase Burnham Center for Chemical Genomics 08/01/11
aid488906 Dose Response confirmation of uHTS inhibitors of Mouse Intestinal Alkaline Phosphatase using Tissue Nonspecific Alkaline Phosphatase. Burnham Center for Chemical Genomics 08/01/11
aid488865 Dose Response screen for agonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule agonists hits of the APJ receptor Burnham Center for Chemical Genomics 08/01/11
aid463220 Dose Response: Fluorescence polarization-based cell-based high throughput dose response assay for inhibitors of insulin-degrading enzyme (IDE) The Scripps Research Institute Molecular Screening Center 08/01/11
aid485352 HTS Dose response counterscreen for assays utilizing the enzyme, beta-galactosidase - Set 2 Burnham Center for Chemical Genomics 08/01/11
aid489005 Inhibitors of T-Type Calcium Channel Vanderbilt Screening Center for GPCRs, Ion Channels and Transporters 08/01/11
aid485336 Late stage assay provider counterscreen results from the probe development effort to identify inhibitors of kruppel-like factor 5 (KLF5): chemiluminescence-based western blot assay for inhibitors of KLF5 protein levels The Scripps Research Institute Molecular Screening Center 08/01/11
aid463225 Late-stage fluorescence dose response cell-based counterscreening assay for antagonists of the Sphingosine 1-Phosphate Receptor 4 (S1P4): inhibition by S1P4-selective antagonist The Scripps Research Institute Molecular Screening Center 08/01/11
aid463250 Late-stage fluorescence-based counterscreen for antagonists of the G-protein coupled receptor 7 (GPR7): cell-based dose response assay to identify antagonists of the melanin-concentrating hormone receptor 1 (MCHR1) The Scripps Research Institute Molecular Screening Center 08/01/11
aid463251 Late-stage fluorescence-based dose response cell-based screening assay to identify antagonists of the G-protein coupled receptor 7 (GPR7) The Scripps Research Institute Molecular Screening Center 08/01/11
aid485339 Late-stage fluorescence-based dose response cell-based screening assay to identify antagonists of the G-protein coupled receptor 7 (GPR7): Intracellular calcium release The Scripps Research Institute Molecular Screening Center 08/01/11
aid463217 SAR Analysis for the identification of Selective Antagonists of ERK1/2 Activity in GPR35-Overexpressing U2OS Cells Burnham Center for Chemical Genomics 08/01/11
aid488987 SAR Analysis for the identification of Selective Antagonists of ERK1/2 Activity in GPR35-Overexpressing U2OS Cells - Set 2 Burnham Center for Chemical Genomics 08/01/11
aid488824 SAR Analysis of Agonists of the DOR Receptor using an Image-Based Assay - Set 3 Burnham Center for Chemical Genomics 08/01/11
aid488822 SAR Analysis of Agonists of the MOR Receptor using an Image-Based Assay - Set 3 Burnham Center for Chemical Genomics 08/01/11
aid488831 SAR Analysis of Antagonists of the DOR Receptor using an Image-Based Assay - Set 3 Burnham Center for Chemical Genomics 08/01/11
aid488842 SAR Analysis of Antagonists of the MOR Receptor using an Image-Based Assay - Set 3 Burnham Center for Chemical Genomics 08/01/11
aid463228 SAR Analysis of Selective Antagonists of GPR55 using an Image-Based Assay - Set 3 Burnham Center for Chemical Genomics 08/01/11
aid485287 SAR Analysis of Selective Antagonists of GPR55 using an Image-Based Assay - Set 4 Burnham Center for Chemical Genomics 08/01/11
aid488791 SAR Confirmatory Dose Response LIBS Assay for Allosteric Ligands of the VLA-4 Integrin NMMLSC 08/01/11
aid488869 SAR LYP1 Fluorescent Assay using OMFP substrate for In Vitro dose response studies - Set 4 Burnham Center for Chemical Genomics 08/01/11
aid488871 SAR LYP1 Fluorescent Assay using pCAP substrate for In Vitro dose response studies - Set 4 Burnham Center for Chemical Genomics 08/01/11
aid488884 SAR Selectivity Analysis of small molecule inhibitors of PEST using pCAP in a fluorescence assay Burnham Center for Chemical Genomics 08/01/11
aid485286 SAR analysis of Agonists of the GPR35 Receptor using an Image-Based Assay - Set 4 Burnham Center for Chemical Genomics 08/01/11
aid488833 SAR analysis of Agonists of the Kappa Opioid Receptor (KOR) using an Image-Based Assay-Set 3 Burnham Center for Chemical Genomics 08/01/11
aid488957 SAR analysis of Antagonists of IAP-family anti-apoptotic proteins - Set 2 Burnham Center for Chemical Genomics 08/01/11
aid488963 SAR analysis of Antagonists of XIAP-Bir3 domain of IAP-family anti-apoptotic proteins - Set 2 Burnham Center for Chemical Genomics 08/01/11
aid463227 SAR analysis of Antagonists of the GPR35 Receptor using an Image-Based Assay - Set 5 Burnham Center for Chemical Genomics 08/01/11
aid485283 SAR analysis of Antagonists of the GPR35 Receptor using an Image-Based Assay - Set 6 Burnham Center for Chemical Genomics 08/01/11
aid488819 SAR analysis of Antagonists of the Kappa Opioid Receptor (KOR) using an Image-Based Assay - Set 3 Burnham Center for Chemical Genomics 08/01/11
aid488925 SAR analysis of Antagonists of the Kappa Opioid Receptor (KOR) using an Image-Based Assay - Set 4 Burnham Center for Chemical Genomics 08/01/11
aid485282 SAR analysis of agonists of the Cannabinoid Receptor 1 using an Image-Based Assay - Set 4 Burnham Center for Chemical Genomics 08/01/11
aid485277 SAR analysis of agonists of the Cannabinoid Receptor 2 using an Image-Based Assay - Set 3 Burnham Center for Chemical Genomics 08/01/11
aid485285 SAR analysis of antagonists of the Cannabinoid Receptor 1 using an Image-Based Assay - Set 4 Burnham Center for Chemical Genomics 08/01/11
aid485278 SAR analysis of antagonists of the Cannabinoid Receptor 2 using an Image-Based Assay - Set 3 Burnham Center for Chemical Genomics 08/01/11
aid488826 SAR analysis of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay - Set 5 Burnham Center for Chemical Genomics 08/01/11
aid488935 SAR analysis of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay - Set 6 Burnham Center for Chemical Genomics 08/01/11
aid463256 TR-FRET-based biochemical high throughput dose response assay to identify NR2E3 inverse agonists The Scripps Research Institute Molecular Screening Center 08/01/11
aid463108 Counterscreen for Oxytocin Receptor (OXTR) agonists: Fluorescence-based cell-based high throughput dose response assay to identify agonists of the vasopressin 1 receptor (V1R) The Scripps Research Institute Molecular Screening Center 07/31/11
aid463128 Counterscreen for vasopressin 1 receptor (V1R) agonists: Fluorescence-based cell-based high throughput dose response assay for agonists of the Oxytocin Receptor (OXTR) The Scripps Research Institute Molecular Screening Center 07/31/11
aid449765 Discovery of a Highly Selective in vitro and in vivo M4 Positive Allosteric Modulator(PAM) : Activity with human M4 Vanderbilt Screening Center for GPCRs, Ion Channels and Transporters 07/31/11
aid463120 Dose Response concentration confirmation of uHTS hits from a small molecule activators of human intestinal alkaline phosphatase via a luminescent assay Burnham Center for Chemical Genomics 07/31/11
aid435032 Dose Response confirmation of HTS hits from an HePTP Fluorescent Assay using OMFP substrate - Set 2 Burnham Center for Chemical Genomics 07/31/11
aid435024 Dose Response confirmation of uHTS hits from a small molecule inhibitors of LYP via a fluorescence intensity assay - Set 2 Burnham Center for Chemical Genomics 07/31/11
aid435027 Dose Response confirmation of uHTS hits from a small molecule inhibitors of LYP via a fluorescence intensity assay using pCAP substrate Burnham Center for Chemical Genomics 07/31/11
aid463135 Dose Response confirmation of uHTS hits from a small molecule inhibitors of human intestinal alkaline phosphatase via a luminescent assay Burnham Center for Chemical Genomics 07/31/11
aid449766 Dose Response of primary screening hit compounds for Identification of VLA-4 Allosteric Modulators NMMLSC 07/31/11
aid463214 Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor Burnham Center for Chemical Genomics 07/31/11
aid435026 Fluorescence Cell-Free Homogeneous Counterscreen to Identify Inhibitors of the RanGTP-Importin-beta complex. Broad Institute 07/31/11
aid435023 Fluorescence Polarization Cell-Free Homogeneous Dose Retest to Confirm Inhibitors of the LANA Histone H2A/H2B Interaction Broad Institute 07/31/11
aid463103 Fluorescence-based cell-based high throughput dose response assay for agonists of the Oxytocin Receptor (OXTR) The Scripps Research Institute Molecular Screening Center 07/31/11
aid463125 Fluorescence-based cell-based high throughput dose response assay for potentiators of Oxytocin Receptor (OXTR) The Scripps Research Institute Molecular Screening Center 07/31/11
aid463127 Fluorescence-based cell-based high throughput dose response screening assay for agonists of the vasopressin 1 receptor (V1R) The Scripps Research Institute Molecular Screening Center 07/31/11
aid435017 High throughput discovery of novel modulators of ROMK K+ channel activity: Analog Library Testing Vanderbilt Screening Center for GPCRs, Ion Channels and Transporters 07/31/11
aid463182 High throughput fluorescence intensity-based biochemical assay to screen for small molecule inhibitors of Furin:Concentration-response Confirmation Assays University of Pittsburgh Molecular Library Screening Center 07/31/11
aid463081 Late stage assay provider results from the probe development effort to identify inhibitors of GSTO1: Gel-based activity-based protein profiling (ABPP) IC50 The Scripps Research Institute Molecular Screening Center 07/31/11
aid463142 Late stage assay provider results from the probe development effort to identify inhibitors of GSTO1: Gel-based activity-based protein profiling (ABPP) IC50 Set 2 The Scripps Research Institute Molecular Screening Center 07/31/11
aid463124 Late stage assay provider results from the probe development effort to identify inhibitors of protein phosphatase methylesterase 1 (PME-1): Gel-based Activity-Based Protein Profiling (ABPP) IC50 Set 2 The Scripps Research Institute Molecular Screening Center 07/31/11
aid435013 Late stage results from the probe development effort to identify inhibitors of (NADPH oxidase 1) NOX1: Family selectivity: Set 2 The Scripps Research Institute Molecular Screening Center 07/31/11
aid463107 Late-stage fluorescence dose-response cell-based assay to identify agonists of the Sphingosine 1-Phosphate Receptor 4 (S1P4): Synthesized compounds The Scripps Research Institute Molecular Screening Center 07/31/11
aid463118 Late-stage fluorescence-based dose-response cell-based assay to identify agonists of the Sphingosine 1-Phosphate Receptor 4 (S1P4): Sphingosine 1-Phosphate Receptor 1 (S1P1) counterscreen assay The Scripps Research Institute Molecular Screening Center 07/31/11
aid463122 Late-stage fluorescence-based dose-response cell-based assay to identify agonists of the Sphingosine 1-Phosphate Receptor 4 (S1P4): Sphingosine 1-Phosphate Receptor 2 (S1P2) counterscreen assay The Scripps Research Institute Molecular Screening Center 07/31/11
aid463123 Late-stage fluorescence-based dose-response cell-based assay to identify agonists of the Sphingosine 1-Phosphate Receptor 4 (S1P4): Sphingosine 1-Phosphate Receptor 3 (S1P3) counterscreen assay The Scripps Research Institute Molecular Screening Center 07/31/11
aid463129 Late-stage fluorescence-based dose-response cell-based assay to identify agonists of the Sphingosine 1-Phosphate Receptor 4 (S1P4): Sphingosine 1-Phosphate Receptor 5 (S1P5) counterscreen assay The Scripps Research Institute Molecular Screening Center 07/31/11
aid463088 Luminescence-based cell-based high throughput dose response assay for activators of the Aryl Hydrocarbon Receptor (AHR) The Scripps Research Institute Molecular Screening Center 07/31/11
aid463086 Luminescence-based counterscreen for activators of the Aryl Hydrocarbon Receptor (AHR): cell-based high throughput dose response screening assay for activators of the Pregnane X Receptor (PXR) The Scripps Research Institute Molecular Screening Center 07/31/11
aid435014 Measurement of GPCR-mediated thallium flux through GIRK channels: Dose-Response Testing Vanderbilt Screening Center for GPCRs, Ion Channels and Transporters 07/31/11
aid435016 Measurement of GPCR-mediated thallium flux through GIRK channels: Dose-Response with Rauwolscine Vanderbilt Screening Center for GPCRs, Ion Channels and Transporters 07/31/11
aid449726 SAR LYP1 Fluorescent Assay using OMFP substrate for In Vitro dose response studies - Set 3 Burnham Center for Chemical Genomics 07/31/11
aid449727 SAR LYP1 Fluorescent Assay using pCAP substrate for In Vitro dose response studies - Set 3 Burnham Center for Chemical Genomics 07/31/11
aid435018 SAR analysis for the identification of translation initiation inhibitors (PABP) Burnham Center for Chemical Genomics 07/31/11
aid435011 SAR analysis for the identification of translation initiation inhibitors (eIF4H) Burnham Center for Chemical Genomics 07/31/11
aid449736 SAR analysis of compounds that inhibit HePTP - Set 2 Burnham Center for Chemical Genomics 07/31/11
aid435029 SAR analysis of compounds that inhibit Human Immunodeficiency Virus Fusion, cell-cell fusion assay Burnham Center for Chemical Genomics 07/31/11
aid449733 SAR analysis of compounds that inhibit VHR1, Fluorescent Assay - Set 2 Burnham Center for Chemical Genomics 07/31/11
aid449737 SAR analysis of small molecule agonists of the kappa opioid receptor via a luminescent beta-arrestin assay - Set 3 Burnham Center for Chemical Genomics 07/31/11
aid463105 SAR analysis of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay - Set 4 Burnham Center for Chemical Genomics 07/31/11
aid434976 Counterscreen for inhibitors of gld-1: Fluorescence polarization-based biochemical high throughput dose response assay for inhibitors of the HIV Rev protein-RRE RNA interaction The Scripps Research Institute Molecular Screening Center 07/30/11
aid434968 Fluorescence Cell-Free Homogeneous Counter Screen to Identify Inhibitors of GFP Chromophore Formation Broad Institute 07/30/11
aid435010 Fluorescence Cell-Free Homogeneous Dose Retest to Identify Inhibitors of RecA-Intein Splicing Activity Broad Institute 07/30/11
aid435009 Late stage results from the probe development effort to identify inhibitors of (NADPH oxidase 1) NOX1: Xanthine Oxidase Set 2 The Scripps Research Institute Molecular Screening Center 07/30/11
aid435002 Late stage results from the probe development effort to identify inhibitors of NOX1: HEK/293 IC50 Set 2 The Scripps Research Institute Molecular Screening Center 07/30/11
aid434957 Late stage results from the probe development effort to identify inhibitors of kruppel-like factor 5 (KLF5): luminescence-based cell-based dose response assay for inhibitors of KLF5 (Round 1) The Scripps Research Institute Molecular Screening Center 07/30/11
aid435004 Luminescence Cell-Based Dose Retest to Identify Potentiators of Heat Shock Factor 1 (HSF1) Broad Institute 07/30/11
aid434997 Luminescence-based cell-based dose response assay to identify inhibitors of NADPH oxidase 1 (NOX1): Cherry picks 2 The Scripps Research Institute Molecular Screening Center 07/30/11
aid434967 SAR analysis of compounds that inhibit Human Immunodeficiency Virus Fusion. Burnham Center for Chemical Genomics 07/30/11
aid434981 SAR analysis of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay - Set 3 Burnham Center for Chemical Genomics 07/30/11
aid434980 SAR analysis of small molecule inhibitors of Mint-PDZ and N-type Ca2+ channel carboxyl-terminal peptide association using HTRF - Set 2 Burnham Center for Chemical Genomics 07/30/11
aid434943 Absorbance Microorganism Dose Response to Identify Inhibitors of Vibrio harveyi Broad Institute 07/29/11
aid434935 Fluorescence Cell-Based Secondary Assay of Resistant C. albicans Growth in the Presence of Fluconazole Broad Institute 07/29/11
aid434945 Fluorescence Cell-Based Secondary Assay to Identify Inhibitors of Calcineurin Broad Institute 07/29/11
aid434940 Late stage counterscreen results from the probe development effort to identify activators of signal transducer and activator of transcription 1 (STAT1): luminescence-based cell-based dose response assay for STAT3 activators The Scripps Research Institute Molecular Screening Center 07/29/11
aid434932 Late stage results from the probe development effort to identify activators of signal transducer and activator of transcription 1 (STAT1): luminescence-based cell-based dose response assay for STAT1 activators The Scripps Research Institute Molecular Screening Center 07/29/11
aid434938 Luminescence Cell-Based Secondary Assay to Identify Inhibitors of Hsp90 Broad Institute 07/29/11
aid434944 Luminescence Cell-Free Homogeneous Dose Response to Identify Inhibitors of Lux-S Broad Institute 07/29/11
aid434954 Luminescence Cell-Free Homogeneous Dose Retest to Identify Inhibitors of Glycogen Synthase Kinase-3 beta Activity Broad Institute 07/29/11
aid434924 SAR analysis of Agonists of the GPR35 Receptor using an Image-Based Assay - Set 3 Burnham Center for Chemical Genomics 07/29/11
aid434925 SAR analysis of Antagonists of the GPR35 Receptor using an Image-Based Assay - Set 4 Burnham Center for Chemical Genomics 07/29/11
aid434928 SAR analysis of agonists of the Cannabinoid Receptor 2 using an Image-Based Assay - Set 2 Burnham Center for Chemical Genomics 07/29/11
aid434929 SAR analysis of antagonists of the Cannabinoid Receptor 1 using an Image-Based Assay - Set 3 Burnham Center for Chemical Genomics 07/29/11
aid434922 SAR analysis of antagonists of the Cannabinoid Receptor 2 using an Image-Based Assay - Set 2 Burnham Center for Chemical Genomics 07/29/11
aid2784 Dose Response confirmation of uHTS hits from a small molecule antagonists of the APJ receptor via a luminescent beta-arrestin assay Sanford-Burnham Center for Chemical Genomics 07/12/11
aid2828 Dose response, multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS16-Galphao with additional round of SAR compounds NMMLSC 07/12/11
aid2829 Dose response, multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS4-Galphao with additional round of SAR compounds. NMMLSC 07/12/11
aid2826 Dose response, multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS7-Galphao with additional round of SAR compounds. NMMLSC 07/12/11
aid2827 Dose response, multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS8-Galphao with additional round of SAR compounds NMMLSC 07/12/11
aid2841 Dose-response primary assay and counterscreen assay for HTS small molecule inhibitors of CHOP to regulate the unfolded protein response to ER stress Emory University Molecular Libraries Screening Center 07/12/11
aid2802 Fluorescence polarization-based biochemical high throughput dose response assay for inhibitors of GLD-1 protein - TGE RNA interaction The Scripps Research Institute Molecular Screening Center 07/12/11
aid2771 Late stage counterscreen results from the probe development effort to identify STAT1 inhibitors: luminescence-based cell-based dose response assay for STAT3 inhibitors The Scripps Research Institute Molecular Screening Center 07/12/11
aid2772 Late stage results from the probe development effort to identify STAT1 inhibitors: luminescence-based cell-based dose response assay for STAT1 inhibitors The Scripps Research Institute Molecular Screening Center 07/12/11
aid2808 Late-stage luminescence-based cell-based dose response assay to identify inhibitors of NADPH oxidase 1 (NOX1): Purchased analogs The Scripps Research Institute Molecular Screening Center 07/12/11
aid2819 Late-stage luminescence-based cell-based dose response assay to identify inhibitors of NADPH oxidase 1 (NOX1): Purchased analogs 2 The Scripps Research Institute Molecular Screening Center 07/12/11
aid2773 Late-stage luminescence-based cell-based dose response assay to identify inhibitors of NADPH oxidase 1 (NOX1): Synthesized analogs 3 The Scripps Research Institute Molecular Screening Center 07/12/11
aid2821 Luminescence Cell-Free Homogenous Dose Retest to Identify Inhibitors of Serine/Threonine Kinase 33 Activity Broad Institute 07/12/11
aid2793 SAR analysis of NF-kappaB dependent luciferase using DAP as an inducer - Set 2 Burnham Center for Chemical Genomics 07/12/11
aid2789 SAR analysis of NF-kappaB dependent luciferase using Doxorucibin as an inducer - Set 2 Burnham Center for Chemical Genomics 07/12/11
aid2792 SAR analysis of NF-kappaB dependent luciferase using PMA/Ionomycin as an inducer - 2 Burnham Center for Chemical Genomics 07/12/11
aid2798 SAR analysis of compounds that inhibit NOD1 - Set 3 Burnham Center for Chemical Genomics 07/12/11
aid2799 SAR analysis of compounds that inhibit NOD2 - Set 3 Burnham Center for Chemical Genomics 07/12/11
aid2801 SAR analysis of inhibitors of TNFa specific NF-kB induction - Set 3 Burnham Center for Chemical Genomics 07/12/11
aid2723 Absorbance Microorganism Dose Retest to Identify Inhibitors of Vibrio harveyi Broad Institute 07/11/11
aid2470 Absorbance Microorganism-Based Dose Response Followup to Identify Inhibitors of Streptokinase Expression. Broad Institute 07/11/11
aid2725 Absorbance Microorganism-Based Dose Retest to Identify Inhibitors of Vibrio harveyi Broad Institute 07/11/11
aid2594 Confirmation dose response assay for compounds that inhibit/block inward-rectifying potassium ion channel Kir2.1 Johns Hopkins Ion Channel Center 07/11/11
aid2759 Counterscreen for agonists of nuclear receptor subfamily 2, group E, member 3 (NR2E3): TR-FRET-based biochemical high throughput dose response assay to identify agonists of the interaction between peroxisome proliferator-activated receptor gamma (PPARg) and nuclear receptor co-repressor 2 (NCOR2) The Scripps Research Institute Molecular Screening Center 07/11/11
aid2651 Discovery of Novel Allosteric Modulators of the M1 Muscarinic Receptor: PAM Calcium Assay SAR Vanderbilt Screening Center for GPCRs, Ion Channels and Transporters 07/11/11
aid2428 Discovery of novel allosteric modulators of the M1 muscarinic receptor: PAM Calcium Assay Dose-Response with M3 Vanderbilt Screening Center for GPCRs, Ion Channels and Transporters 07/11/11
aid2638 Dosage response for compounds that protect hERG from block by proarrhythmic agents using manual patch clamp Johns Hopkins Ion Channel Center 07/11/11
aid2743 Dose Response of TOR pathway GFP-fusion proteins in Saccharomyes cerevisiae specifically AGP1 based on MLPCN hits NMMLSC 07/11/11
aid2744 Dose Response of TOR pathway GFP-fusion proteins in Saccharomyes cerevisiae specifically CIT2 based on MLPCN hits NMMLSC 07/11/11
aid2745 Dose Response of TOR pathway GFP-fusion proteins in Saccharomyes cerevisiae specifically LAP4 based on MLPCN hits NMMLSC 07/11/11
aid2742 Dose Response of TOR pathway GFP-fusion proteins in Saccharomyes cerevisiae specifically MEP2 based on MLPCN hits NMMLSC 07/11/11
aid2740 Dose Response of TOR pathway GFP-fusion proteins in Saccharomyes cerevisiae specifically RPL19A based on MLPCN hits NMMLSC 07/11/11
aid2654 Dose response of Retigabine-insensitive compounds that potentiate KCNQ2 potassium channel Johns Hopkins Ion Channel Center 07/11/11
aid2755 Epi-absorbance-based dose response assay for common IMP-1 and VIM-2 inhibitors: biochemical high throughput counterscreen to identify inhibitors of TEM-1 metallo-beta-lactamase The Scripps Research Institute Molecular Screening Center 07/11/11
aid2756 Epi-absorbance-based dose response assay for common IMP-1 and VIM-2 inhibitors: biochemical high throughput screening assay to identify inhibitors of IMP-1metallo-beta-lactamase The Scripps Research Institute Molecular Screening Center 07/11/11
aid2754 Epi-absorbance-based dose response assay for common IMP-1 and VIM-2 inhibitors: biochemical high throughput screening assay to identify inhibitors of VIM-2 metallo-beta-lactamase The Scripps Research Institute Molecular Screening Center 07/11/11
aid2579 G6DPH counterscreen for TbHK1 inhibitors - Analogues series University of Pittsburgh Molecular Library Screening Center 07/11/11
aid2485 HTS dose response assay for identification of inhibitors of TNFa-specific NF-kB induction Burnham Center for Chemical Genomics 07/11/11
aid2583 Late stage counterscreen for the probe development effort to identify selective agonists of the Transient Receptor Potential Channels 3 (TRPML3): fluorescence-based cell-based dose response assay for TRPN1 agonists. The Scripps Research Institute Molecular Screening Center 07/11/11
aid2556 Late stage results from the probe development effort to identify inhibitors of (NADPH oxidase 1) NOX1: Xanthine Oxidase The Scripps Research Institute Molecular Screening Center 07/11/11
aid2532 Late stage results from the probe development effort to identify inhibitors of NOX1: HEK/293 IC50 The Scripps Research Institute Molecular Screening Center 07/11/11
aid2510 Late stage results from the probe development effort to identify selective agonists of the Transient Receptor Potential Channels 3 (TRPML3): fluorescence-based cell-based dose response assay for TRPML3 agonists The Scripps Research Institute Molecular Screening Center 07/11/11
aid2664 Late-stage luminescence-based cell-based dose response assay to identify inhibitors of NADPH oxidase 1 (NOX1): Synthesized analogs The Scripps Research Institute Molecular Screening Center 07/11/11
aid2752 Late-stage luminescence-based cell-based dose response assay to identify inhibitors of NADPH oxidase 1 (NOX1): Synthesized analogs 2 The Scripps Research Institute Molecular Screening Center 07/11/11
aid2765 Luminescence Cell-Based Dose Retest to Identify Inhibitors of A1 Apoptosis Broad Institute 07/11/11
aid2735 Luminescence Microorganism Dose Retest to Identify Inhibitors of the AI-2 Quorum Sensing System Broad Institute 07/11/11
aid2724 Luminescence Microorganism-Based Dose Retest to Identify Modulators of the AI-2 Quorum Sensing System Broad Institute 07/11/11
aid2538 Luminescence-based cell-based dose response assay to identify inhibitors of NADPH oxidase 1 (NOX1) The Scripps Research Institute Molecular Screening Center 07/11/11
aid2443 Mode of action - deactivation constant concentration response for ztz240, a potentiator of KCNQ2 potassium channels Johns Hopkins Ion Channel Center 07/11/11
aid2603 Mode of action assay-Automated electrophysiology assay of compounds that potentiate KCNQ2 potassium channel Johns Hopkins Ion Channel Center 07/11/11
aid2493 SAR Analysis of Agonists of the DOR Receptor using an Image-Based Assay - Set 2 Burnham Center for Chemical Genomics 07/11/11
aid2492 SAR Analysis of Agonists of the MOR Receptor using an Image-Based Assay - Set 2 Burnham Center for Chemical Genomics 07/11/11
aid2686 SAR LYP1 Fluorescent Assay using OMFP substrate for In Vitro dose response studies - Set 2 Burnham Center for Chemical Genomics 07/11/11
aid2682 SAR LYP1 Fluorescent Assay using pCAP substrate for In Vitro dose response studies - Set 2 Burnham Center for Chemical Genomics 07/11/11
aid2497 SAR analysis of Agonists of the Kappa Opioid Receptor (KOR) using an Image-Based Assay - Set 2 Burnham Center for Chemical Genomics 07/11/11
aid2480 SAR analysis of Antagonists of the GPR35 Receptor using an Image-Based Assay - Set 2 Burnham Center for Chemical Genomics 07/11/11
aid2491 SAR analysis of Antagonists of the Kappa Opioid Receptor (KOR) using an Image-Based Assay - Set 2 Burnham Center for Chemical Genomics 07/11/11
aid2505 SAR analysis of GM-Tri-DAP induced IL-8 secretion in MCF-7/NOD1 cells - Set 2 Burnham Center for Chemical Genomics 07/11/11
aid2503 SAR analysis of Muramyl dipeptide (MDP) induced IL-8 secretion in MCF-7/NOD2 cells - Set 2 Burnham Center for Chemical Genomics 07/11/11
aid2504 SAR analysis of Tumor necrosis factor alpha (TNF-alpha) induced IL-8 secretion in MCF-7/NOD1 cells - Set 2 Burnham Center for Chemical Genomics 07/11/11
aid2466 SAR analysis of compounds that inhibit NOD1 - Set 2 Burnham Center for Chemical Genomics 07/11/11
aid2475 SAR analysis of compounds that inhibit NOD2 - Set 2 Burnham Center for Chemical Genomics 07/11/11
aid2483 SAR analysis of inhibitors of TNFa specific NF-kB induction - Set 2 Burnham Center for Chemical Genomics 07/11/11
aid2500 SAR analysis of small molecule agonists of the kappa opioid receptor via a luminescent beta-arrestin assay - Set 2 Burnham Center for Chemical Genomics 07/11/11
aid2489 SAR analysis of small molecule inhibitors of Mint-PDZ and N-type Ca2+ channel carboxyl-terminal peptide association using HTRF Burnham Center for Chemical Genomics 07/11/11
aid2758 TR-FRET-based biochemical high throughput dose response assay for agonists of nuclear receptor subfamily 2, group E, member 3 (NR2E3) The Scripps Research Institute Molecular Screening Center 07/11/11
aid2377 Counterscreen for inhibitors of EBNA-1: fluorescence polarization-based biochemical high throughput dose response assay to identify inhibitors of the Epstein-Barr virus-encoded protein, ZTA The Scripps Research Institute Molecular Screening Center 07/10/11
aid2422 Counterscreen for inhibitors of PP1: fluorescence-based biochemical high throughput dose response assay to identify inhibitors of Protein Phosphatase 5 (PP5) The Scripps Research Institute Molecular Screening Center 07/10/11
aid2394 Counterscreen for inhibitors of PP5: fluorescence-based biochemical high throughput dose response assay for inhibitors of Protein Phosphatase 1 (PP1) The Scripps Research Institute Molecular Screening Center 07/10/11
aid2423 Fluorescence Cell-Based Secondary Assay to Identify Inhibitors of Resistant C. albicans Growth in the Presence of Fluconazole Broad Institute 07/10/11
aid2387 Fluorescence Cell-Based Secondary Assay to Measure Toxicity of Compounds Not in the Presence of Fluconazole Broad Institute 07/10/11
aid2381 Fluorescence polarization-based biochemical high throughput dose response assay for inhibitors of the Epstein-Barr virus nuclear antigen 1 (EBNA-1) The Scripps Research Institute Molecular Screening Center 07/10/11
aid2395 Fluorescence-based biochemical high throughput dose response assay for inhibitors of Protein Phosphatase 5 (PP5) The Scripps Research Institute Molecular Screening Center 07/10/11
aid2403 Fluorescence-based biochemical high throughput dose response assay to identify inhibitors of Protein Phosphatase 1 (PP1) The Scripps Research Institute Molecular Screening Center 07/10/11
aid2343 HTS Image-Based Screen for Agonists of the DOR Receptor Burnham Center for Chemical Genomics 07/10/11
aid2356 HTS Image-Based Screen for Antagonists of the DOR Receptor Burnham Center for Chemical Genomics 07/10/11
aid2351 Late stage counterscreen assay for S1P4 antagonists: Fluorescence dose response cell-based screening assay for antagonists of the Sphingosine 1-Phosphate Receptor 1 (S1P1) The Scripps Research Institute Molecular Screening Center 07/10/11
aid2354 Late stage counterscreen assay for S1P4 antagonists: Fluorescence dose response cell-based screening assay for antagonists of the Sphingosine 1-Phosphate Receptor 2 (S1P2) The Scripps Research Institute Molecular Screening Center 07/10/11
aid2349 Late stage counterscreen assay for S1P4 antagonists: Fluorescence dose response cell-based screening assay for antagonists of the Sphingosine 1-Phosphate Receptor 3 (S1P3) The Scripps Research Institute Molecular Screening Center 07/10/11
aid2350 Late stage counterscreen assay for S1P4 antagonists: Fluorescence dose response cell-based screening assay for antagonists of the Sphingosine 1-Phosphate Receptor 5 (S1P5) The Scripps Research Institute Molecular Screening Center 07/10/11
aid2346 Late stage fluorescence dose response cell-based screening assay for antagonists of the Sphingosine 1-Phosphate Receptor 4 (S1P4): Synthesized analogues The Scripps Research Institute Molecular Screening Center 07/10/11
aid2382 Luminescence Cell-Based Dose Confimation HTS to Identify Inhibitors of Heat Shock Factor 1 (HSF1) Broad Institute 07/10/11
aid2388 Luminesence Cell-Based Secondary Assay to Identify Inhibitors of Calcineurin Broad Institute 07/10/11
aid2400 Luminesence Cell-Based Secondary Assay to Identify Inhibitors of Hsp90 Broad Institute 07/10/11
aid2408 Mode of action - current amplitude concentration response for ztz240, a potentiator of KCNQ2 potassium channels Johns Hopkins Ion Channel Center 07/10/11
aid2370 SAR Analysis of Agonists of the DOR Receptor using an Image-Based Assay Burnham Center for Chemical Genomics 07/10/11
aid2352 SAR Analysis of Agonists of the MOR Receptor using an Image-Based Assay Burnham Center for Chemical Genomics 07/10/11
aid2357 SAR Analysis of Antagonists of the DOR Receptor using an Image-Based Assay Burnham Center for Chemical Genomics 07/10/11
aid2420 SAR Analysis of Antagonists of the MOR Receptor using an Image-Based Assay Burnham Center for Chemical Genomics 07/10/11
aid2397 SAR Analysis of Selective Antagonists of GPR55 using an Image-Based Assay Burnham Center for Chemical Genomics 07/10/11
aid2359 SAR analysis of Agonists of the Kappa Opioid Receptor (KOR) using an Image-Based Assay Burnham Center for Chemical Genomics 07/10/11
aid2338 SAR analysis of Antagonists of the GPR35 Receptor using an Image-Based Assay Burnham Center for Chemical Genomics 07/10/11
aid2348 SAR analysis of Antagonists of the Kappa Opioid Receptor (KOR) using an Image-Based Assay Burnham Center for Chemical Genomics 07/10/11
aid2230 Confirmation assay for inhibitors of Trypanosoma brucei hexokinase 1-Analogue-first series University of Pittsburgh Molecular Library Screening Center 07/09/11
aid2214 Counterscreen for inhibitors of M1 and M17 aminopeptidases: QFRET-based biochemical high throughput dose response assay for inhibitors of the Cathepsin L proteinase (CTSL1). The Scripps Research Institute Molecular Screening Center 07/09/11
aid2218 Counterscreen for inhibitors of MCL1: fluorescence polarization-based biochemical high throughput dose response assay for inhibitors of BCL2-related protein, long isoform (BCLXL). The Scripps Research Institute Molecular Screening Center 07/09/11
aid2204 Discovery of Novel Allosteric Modulators of the Muscarinic Receptor M5: Calcium Flux Assay Vanderbilt Screening Center for GPCRs, Ion Channels and Transporters 07/09/11
aid2298 Dose response, multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS16-Galphao for SAR Compounds NMMLSC 07/09/11
aid2311 Dose response, multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS19-Galphao for SAR Compounds NMMLSC 07/09/11
aid2295 Dose response, multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS4-Galphao for SAR compounds NMMLSC 07/09/11
aid2296 Dose response, multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS7-Galphao for SAR Compounds NMMLSC 07/09/11
aid2307 Dose response, multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS8-Galphao for SAR Compounds NMMLSC 07/09/11
aid2207 Fluorescence counterscreen for potentiators or agonists of NPY-Y1: Cell-based high-throughput dose response assay for potentiators or agonists of NPY-Y2. The Scripps Research Institute Molecular Screening Center 07/09/11
aid2217 Fluorescence polarization-based biochemical high throughput dose response assay for inhibitors of myeloid cell leukemia sequence 1 (MCL1) interactions with BIM-BH3 peptide. The Scripps Research Institute Molecular Screening Center 07/09/11
aid2210 Fluorescence-based cell-based high-throughput dose response assay for agonists of NPY-Y2. The Scripps Research Institute Molecular Screening Center 07/09/11
aid2220 Fluorescence-based cell-based high-throughput dose response assay for potentiators or agonists of NPY-Y2. The Scripps Research Institute Molecular Screening Center 07/09/11
aid2219 Fluorescence-based counterscreen for agonists of NPY-Y1: cell-based high-throughput dose response assay for agonists of NPY-Y2. The Scripps Research Institute Molecular Screening Center 07/09/11
aid2212 Fluorescence-based counterscreen for agonists of NPY-Y2: cell-based high-throughput dose response assay for agonists of NPY-Y1. The Scripps Research Institute Molecular Screening Center 07/09/11
aid2211 Fluorescence-based counterscreen for potentiators or agonists of NPY-Y2: cell-based high-throughput dose response assay for potentiators or agonists of NPY-Y1. The Scripps Research Institute Molecular Screening Center 07/09/11
aid2251 Fluorescence-based dose response cell-based high throughput screening assay to identify antagonists of the G-protein coupled receptor 7 (GPR7). The Scripps Research Institute Molecular Screening Center 07/09/11
aid2208 Fluorescence-based dose response cell-based high-throughput screening assay for agonists of NPY-Y1. The Scripps Research Institute Molecular Screening Center 07/09/11
aid2209 Fluorescence-based dose response cell-based high-throughput screening assay for potentiators or agonists of NPY-Y1. The Scripps Research Institute Molecular Screening Center 07/09/11
aid2073 Homogeneous Time-Resolved Fluorescence Resonance Energy Transfer (HTRF) Assay Burnham Center for Chemical Genomics 07/09/11
aid1903 Identification of SV40 T antigen inhibitors: A route to novel anti-viral reagents Southern Research Specialized Biocontainment Screening Center 07/09/11
aid2013 Image-Based HTS for Selective Antagonists for GPR55 Burnham Center for Chemical Genomics 07/09/11
aid2058 Image-Based HTS for Selective Antagonists of GPR35 Burnham Center for Chemical Genomics 07/09/11
aid1961 Image-based HTS for Selective Agonists of GPR55 Burnham Center for Chemical Genomics 07/09/11
aid2332 Late stage fluorescence dose response cell-based screening assay for antagonists of the Sphingosine 1-Phosphate Receptor 4 (S1P4) The Scripps Research Institute Molecular Screening Center 07/09/11
aid2264 SAR analysis of NF-kB dependent luciferase using DAP as an inducer Burnham Center for Chemical Genomics 07/09/11
aid2333 SAR analysis of compounds that inhibit NOD1 revised Burnham Center for Chemical Genomics 07/09/11
aid2334 SAR analysis of compounds that inhibit NOD2 revised Burnham Center for Chemical Genomics 07/09/11
aid2337 SAR analysis of inhibitors of TNFa specific NF-kB induction revised Burnham Center for Chemical Genomics 07/09/11
aid2284 SAR analysis of small molecule agonists of the kappa opioid receptor via a luminescent beta-arrestin assay Burnham Center for Chemical Genomics 07/09/11
aid2285 SAR analysis of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay Burnham Center for Chemical Genomics 07/09/11
aid2006 uHTS HTRF assay for identification of inhibitors of SUMOylation Burnham Center for Chemical Genomics 07/09/11
aid1654 uHTS absorbance assay for the identification of compounds that inhibit VHR1. Burnham Center for Chemical Genomics 07/09/11
aid2014 uHTS fluorescence polarization assay for the identification of translation initiation inhibitors (PABP) Burnham Center for Chemical Genomics 07/09/11
aid2012 uHTS fluorescence polarization assay for the identification of translation initiation inhibitors (eIF4H) Burnham Center for Chemical Genomics 07/09/11
aid1817 uHTS identification of small molecule antagonists of the binding of Siah-1 and a peptide ligand via a fluorescence polarization assay. Burnham Center for Chemical Genomics 07/09/11
aid1778 uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay Burnham Center for Chemical Genomics 07/09/11
aid1779 uHTS identification of small molecule inhibitors of LYP via a fluorescence intensity assay Burnham Center for Chemical Genomics 07/09/11
aid1018 Chemical Antagonists IAP-family anti-apoptotic proteins Sanford-Burnham Center for Chemical Genomics 07/08/11
aid1619 Inhibitors of Plasmodium falciparum M17- Family Leucine Aminopeptidase (M17LAP) SRMLSC 07/08/11
aid696 Luminescent assay for HTS discovery of chemical activators of placental alkaline phosphatase Burnham Center for Chemical Genomics 07/08/11
aid1001 uHTS identification of compounds activating TNAP in the absence of phosphate acceptor performed in luminescent assay Sanford-Burnham Center for Chemical Genomics 07/08/11
aid1578 uHTS luminescence assay for the identification of compounds that inhibit NOD1 Burnham Center for Chemical Genomics 07/08/11
aid2102 Identification of SV40 T antigen inhibitors: Cytotoxicity screen of selected hits Southern Research Specialized Biocontainment Screening Center 06/09/11
aid2009 Oxadiazole SAR compounds tested by Multiplex dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Cdc42 activated mutant NMMLSC 06/09/11
aid1914 Absorbance Microorganism-Based Dose Response HTS to Identify Inhibitors of Streptokinase Expression Broad Institute 06/08/11
aid1435 Homologous Recombination - Rad 51_Dose response PCMD 06/08/11
aid1431 Kallikrein 5 1536 HTS Dose Response Confirmation PCMD 06/08/11
aid1275 Dose Response Confirmation for small molecular inhibitors for p47phox, a regulatory protein of NADPH oxidases (Noxs) Emory University Molecular Libraries Screening Center 06/07/11
aid2137 Absorbance Microorganism-Based Dose Response Followup to Identify Inhibitors of Streptokinase Expression Broad Institute 06/05/11
aid2021 Additional SAR compounds tested by Multiplex dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Cdc42 activated mutant NMMLSC 06/05/11
aid2022 Additional SAR compounds tested via Multiplex dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Cdc42 wildtype NMMLSC 06/05/11
aid2046 Additional SAR compounds tested via Multiplex dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Rab2 wildtype NMMLSC 06/05/11
aid2036 Additional SAR compounds tested via Multiplex dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Rab7 wildtype NMMLSC 06/05/11
aid2039 Additional SAR compounds tested via Multiplex dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Rac1 activated mutant NMMLSC 06/05/11
aid2040 Additional SAR compounds tested via Multiplex dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Rac1 wildtype NMMLSC 06/05/11
aid2043 Additional SAR compounds tested via Multiplex dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Ras activated mutant NMMLSC 06/05/11
aid2038 Additional SAR compounds tested via Multiplex dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Ras wildtype NMMLSC 06/05/11
aid2018 AlphaScreen confirmatory assay for validation of inhibitors of SUMOylation Burnham Center for Chemical Genomics 06/05/11
aid2075 Confirmation dose response of hits from multiplexed high-throughput screen for small molecule regulators of Bcl-2 family protein interactions, specifically Bim-Bcl-2 NMMLSC 06/05/11
aid2077 Confirmation dose response of hits from multiplexed high-throughput screen for small molecule regulators of Bcl-2 family protein interactions, specifically Bim-Bcl-B NMMLSC 06/05/11
aid2081 Confirmation dose response of hits from multiplexed high-throughput screen for small molecule regulators of Bcl-2 family protein interactions, specifically Bim-Bcl-W NMMLSC 06/05/11
aid2084 Confirmation dose response of hits from multiplexed high-throughput screen for small molecule regulators of Bcl-2 family protein interactions, specifically Bim-Bcl-XL NMMLSC 06/05/11
aid2080 Confirmation dose response of hits from multiplexed high-throughput screen for small molecule regulators of Bcl-2 family protein interactions, specifically Bim-Bfl-1 NMMLSC 06/05/11
aid2086 Confirmation dose response of hits from multiplexed high-throughput screen for small molecule regulators of Bcl-2 family protein interactions, specifically Bim-Mcl-1 NMMLSC 06/05/11
aid2167 Counterscreen for inhibitors of tRNA 2'-phosphotransferase (TPT1): fluorescence polarization-based biochemical high throughput dose response assay to identify inhibitors of RNAse T1. The Scripps Research Institute Molecular Screening Center 06/05/11
aid2186 Discovery of Novel Allosteric Modulators of the Muscarinic Receptor M5: Fold-shift Assay Vanderbilt Screening Center for GPCRs, Ion Channels and Transporters 06/05/11
aid2192 Discovery of Novel Allosteric Modulators of the Muscarinic Receptor M5: [3H]N-methylscopolamine Competition Vanderbilt Screening Center for GPCRs, Ion Channels and Transporters 06/05/11
aid2194 Discovery of Novel Allosteric Modulators of the Muscarinic Receptor M5: [3H]N-methylscopolamine Competition with Acetylcholine Vanderbilt Screening Center for GPCRs, Ion Channels and Transporters 06/05/11
aid2150 Dose Response of SAR compounds via Multiplex HTS Assay for Inhibitors of MEK Kinase PB1 Domains, specifically MEK5 binding to MEK Kinase 2 Wildtype NMMLSC 06/05/11
aid2160 Fluorescence polarization-based biochemical high throughput dose response assay to identify inhibitors of tRNA 2'-phosphotransferase (TPT1). The Scripps Research Institute Molecular Screening Center 06/05/11
aid2173 Fluorescence-based biochemical high throughput dose response assay for inhibitors of the Hepatitis C Virus non-structural protein 3 helicase (NS3). The Scripps Research Institute Molecular Screening Center 06/05/11
aid2141 HTS TR-FRET-based dose response confirmatory assay for Siah-1 Burnham Center for Chemical Genomics 06/05/11
aid2134 HTS HePTP Fluorescent Assay using OMFP substrate for In Vitro dose response studies Burnham Center for Chemical Genomics 06/05/11
aid2133 HTS Image-Based Screen for Selective Agonists of the KOR Receptor Burnham Center for Chemical Genomics 06/05/11
aid2136 HTS Image-Based Screen for Selective Antagonists of the KOR Receptor Burnham Center for Chemical Genomics 06/05/11
aid2127 HTS fluorescence polarization-based dose response confirmatory screen for the Siah-1 primary assay utilizing an alternative fluorophore, fluorescein-labeled plectin Burnham Center for Chemical Genomics 06/05/11
aid2126 LYP1 Fluorescent Assay using OMFP substrate for In Vitro dose response studies. Burnham Center for Chemical Genomics 06/05/11
aid2068 MOA HePTP Fluorescent secondary assay for identification of redox-state modulating compounds Burnham Center for Chemical Genomics 06/05/11
aid2070 MOA VHR1 Fluorescent secondary assay for identification of redox-state modulating compounds Burnham Center for Chemical Genomics 06/05/11
aid2197 Modulation of the Metabotropic Glutamate Receptor mGluR4: Potency at human mGluR4 Vanderbilt Screening Center for GPCRs, Ion Channels and Transporters 06/05/11
aid2185 Modulation of the Metabotropic Glutamate Receptor mGluR4: Rat PAM Potency Vanderbilt Screening Center for GPCRs, Ion Channels and Transporters 06/05/11
aid2193 Modulation of the Metabotropic Glutamate Receptor mGluR4: Selectivity at mGluR1 Vanderbilt Screening Center for GPCRs, Ion Channels and Transporters 06/05/11
aid2188 Modulation of the Metabotropic Glutamate Receptor mGluR4: Selectivity at mGluR2 Vanderbilt Screening Center for GPCRs, Ion Channels and Transporters 06/05/11
aid2190 Modulation of the Metabotropic Glutamate Receptor mGluR4: Selectivity at mGluR3 Vanderbilt Screening Center for GPCRs, Ion Channels and Transporters 06/05/11
aid2183 Modulation of the Metabotropic Glutamate Receptor mGluR4: Selectivity at mGluR4 Vanderbilt Screening Center for GPCRs, Ion Channels and Transporters 06/05/11
aid2199 Modulation of the Metabotropic Glutamate Receptor mGluR4: Selectivity at mGluR5 Vanderbilt Screening Center for GPCRs, Ion Channels and Transporters 06/05/11
aid2191 Modulation of the Metabotropic Glutamate Receptor mGluR4: Selectivity at mGluR6 Vanderbilt Screening Center for GPCRs, Ion Channels and Transporters 06/05/11
aid2182 Modulation of the Metabotropic Glutamate Receptor mGluR4: Selectivity at mGluR7 Vanderbilt Screening Center for GPCRs, Ion Channels and Transporters 06/05/11
aid2181 Modulation of the Metabotropic Glutamate Receptor mGluR4: Selectivity at mGluR8 Vanderbilt Screening Center for GPCRs, Ion Channels and Transporters 06/05/11
aid2037 Oxadiazole SAR compounds tested via Multiplex dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Cdc42 wildtype NMMLSC 06/05/11
aid2033 Oxadiazole SAR compounds tested via Multiplex dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Rab2 wildtype NMMLSC 06/05/11
aid2031 Oxadiazole SAR compounds tested via Multiplex dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Rab7 wildtype NMMLSC 06/05/11
aid2051 Oxadiazole SAR compounds tested via Multiplex dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Rac1 activated mutant NMMLSC 06/05/11
aid2027 Oxadiazole SAR compounds tested via Multiplex dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Rac1 wildtype NMMLSC 06/05/11
aid2042 Oxadiazole SAR compounds tested via Multiplex dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Ras activated mutant NMMLSC 06/05/11
aid2053 Oxadiazole SAR compounds tested via Multiplex dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Ras wildtype NMMLSC 06/05/11
aid2020 Pyrazoline SAR compounds tested via Multiplex dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Cdc42 activated mutant NMMLSC 06/05/11
aid2019 Pyrazoline SAR compounds tested via Multiplex dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Cdc42 wildtype protein NMMLSC 06/05/11
aid2041 Pyrazoline SAR compounds tested via Multiplex dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Rab7 wildtype NMMLSC 06/05/11
aid2048 Pyrazoline SAR compounds tested via Multiplex dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Rac1 activated mutant NMMLSC 06/05/11
aid2055 Pyrazoline SAR compounds tested via Multiplex dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Rac1 wildtype NMMLSC 06/05/11
aid2050 Pyrazoline SAR compounds tested via Multiplex dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Ras activated mutant NMMLSC 06/05/11
aid2047 Pyrazoline SAR compounds tested via Multiplex dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Ras wildtype NMMLSC 06/05/11
aid2195 QFRET-based biochemical high throughput dose response assay for inhibitors of the Plasmodium falciparum M18 Aspartyl Aminopeptidase (PFM18AAP). The Scripps Research Institute Molecular Screening Center 06/05/11
aid2196 QFRET-based counterscreen for inhibitors of PFM18AAP: biochemical high throughput dose response assay for inhibitors of the Cathepsin L proteinase (CTSL1). The Scripps Research Institute Molecular Screening Center 06/05/11
aid2151 SAR Compounds tested by Dose Response Screen via Multiplex HTS Assay for Inhibitors of MEK Kinase PB1 Domains, specifically MEK5 binding to MEK Kinase 2 Mutant. NMMLSC 06/05/11
aid2145 SAR Compounds tested by Dose Response Screen via Multiplex HTS Assay for Inhibitors of MEK Kinase PB1 Domains, specifically MEK5 binding to MEK Kinase 3 Wildtype. NMMLSC 06/05/11
aid2140 SAR LYP1 Fluorescent Assay using OMFP substrate for In Vitro dose response studies Burnham Center for Chemical Genomics 06/05/11
aid2135 SAR LYP1 Fluorescent Assay using pCAP substrate for In Vitro dose response studies Burnham Center for Chemical Genomics 06/05/11
aid2159 TR-FRET-based biochemical high-throughput dose response assay to identify inhibitors of Hepatitis C Virus (HCV) core protein dimerization. The Scripps Research Institute Molecular Screening Center 06/05/11
aid2091 uHTS Homogeneous Terbium Time-Resolved Fluorescence Resonance Energy Transfer (HTRF) Assay Burnham Center for Chemical Genomics 06/05/11
aid2001 uHTS luminescence assay for the identification of compounds that inhibit NOD2 in MDP treated cells Burnham Center for Chemical Genomics 06/05/11
aid702 Dose-Response of Allosteric Antagonists for the VLA-4 Integrin NMMLSC 06/04/11
aid521 HTS Discovery of Chemical Inhibitors of HePTP, a Leukemia Target Burnham Center for Chemical Genomics 06/04/11
aid1209 HTS identification of compounds inhibiting phosphomannose isomerase (PMI) via a fluorescence intensity assay. Sanford-Burnham Center for Chemical Genomics 06/04/11
aid568 High Throughput Screening Assay for Hsc70 Inhibitors Burnham Center for Chemical Genomics 06/04/11
aid1445 Inhibitors of Plasmodium falciparum M1- Family Alanyl Aminopeptidase (M1AAP) SRMLSC 06/04/11
aid425 MKP-3 in vitro HTS assay Sanford-Burnham Center for Chemical Genomics 06/04/11
aid1920 Epi-absorbance-based counterscreen for selective VIM-2 inhibitors: dose response biochemical high throughput screening assay to identify inhibitors of IMP-1 metallo-beta-lactamase. The Scripps Research Institute Molecular Screening Center 06/01/11
aid1919 Epi-absorbance-based dose response biochemical high throughput screening assay for selective inhibitors of VIM-2 metallo-beta-lactamase The Scripps Research Institute Molecular Screening Center 06/01/11
aid1926 FRET-based counterscreen for selective VIM-2 inhibitors: dose response biochemical high throughput screening assay to identify epi-absorbance assay artifacts. The Scripps Research Institute Molecular Screening Center 06/01/11
aid1927 FRET-based counterscreen for selective VIM-2 inhibitors: dose response biochemical high throughput screening assay to identify inhibitors of IMP-1 metallo-beta-lactamase. The Scripps Research Institute Molecular Screening Center 06/01/11
aid1960 Fluorescent Polarization Homogeneous Dose Response HTS to Indentify Inhibitors of Mex-5 Binding to TCR-2 Broad Institute 06/01/11
aid1964 Fluorescent Polarization Homogeneous Dose Response HTS to Indentify Inhibitors of POS-1 Binding to mex-3-RNA Broad Institute 06/01/11
aid1636 Cathepsin L probe #2 dose-response testing PCMD 05/31/11
aid1764 Discovery of novel allosteric modulators of the M1 muscarinic receptor: Agonist NMS competition at M3 Vanderbilt Screening Center for GPCRs, Ion Channels and Transporters 05/31/11
aid1895 Dose Response Confirmation Screen via Multiplex HTS Assay for Inhibitors of MEK Kinase PB1 Domains, specifically MEK5 binding to MEK Kinase 2 Mutant NMMLSC 05/31/11
aid1897 Dose Response Confirmation via Multiplex HTS Assay for Inhibitors of MEK Kinase PB1 Domains, specifically MEK5 binding to MEK Kinase 2 Wildtype NMMLSC 05/31/11
aid1872 Dose response, multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS4-Galphao. NMMLSC 05/31/11
aid1442 E3 Ligase_Mutant_Dose Response PCMD 05/31/11
aid1444 E3 Ligase_WT_Dose Response PCMD 05/31/11
aid1682 Fluorescence counterscreen assay for TRPML3 agonists: dose response cell-based high-throughput screening assay to identify agonists of the transient receptor potential channel N1 (TRPN1) The Scripps Research Institute Molecular Screening Center 05/31/11
aid1660 Fluorescence counterscreen assay for TRPN1 agonists: dose response cell-based high-throughput screening assay to identify agonists of the transient receptor potential channel ML3 (TRPML3) The Scripps Research Institute Molecular Screening Center 05/31/11
aid1878 Fluorescent assay for identification of compounds that inhibit VHR1 Burnham Center for Chemical Genomics 05/31/11
aid1436 Homologous Recombination_Rad51_DNA binding assay PCMD 05/31/11
aid1437 Homologous recombination_Rad 51_dose response_2 PCMD 05/31/11
aid1723 Identification of Novel Modulators of Cl- dependent Transport Process via HTS: Dose-Dependent Assay 2 with KCC2 Vanderbilt Screening Center for GPCRs, Ion Channels and Transporters 05/31/11
aid1695 Rml C and D dose-response confirmation PCMD 05/31/11
aid1659 SAR assay for compounds activating TNAP in the presence of 100 mM DEA performed in a luminescence assay Burnham Center for Chemical Genomics 05/31/11
aid858 Allosteric Modulators of D1 Receptors: Dose-dependent Assay Vanderbilt Screening Center for GPCRs, Ion Channels and Transporters 05/30/11
aid857 Allosteric Modulators of D1 Receptors: Dose-dependent Counterscreen Vanderbilt Screening Center for GPCRs, Ion Channels and Transporters 05/30/11
aid1417 Dose Response Confirmation for Mcl-1/Noxa Interaction Inhibitors Emory University Molecular Libraries Screening Center 05/30/11
aid1419 Dose Response Confirmation for Small Molecule Inhibitors of Epstein-Barr Virus Emory University Molecular Libraries Screening Center 05/30/11
aid855 Dose Response Confirmation for Small Molecule Inhibitors of Eukaryotic Translation Initiation Emory University Molecular Libraries Screening Center 05/30/11
aid733 Estrogen Receptor-beta Coactivator Binding Inhibitors Dose Response Confirmation Emory University Molecular Libraries Screening Center 05/30/11
aid1060 Estrogen Receptor-beta Coactivator Binding Inhibitors ELISA Secondary Assay Emory University Molecular Libraries Screening Center 05/30/11
aid618 Luminescent HTS for small molecule inhibitors of MT1-MMP transcription Sanford-Burnham Center for Chemical Genomics 05/30/11
aid1241 Name: High Throughput Screen to Identify Compounds that increase expression of NF-kB in Human Neuronal Cells - Dose Response SRMLSC 05/30/11
aid1938 Discovery of a Highly Selective in vitro and in vivo M4 Positive Allosteric Modulator (PAM): Analog Dose Response with rM4 Vanderbilt Screening Center for GPCRs, Ion Channels and Transporters 05/29/11
aid1939 Discovery of a Highly Selective in vitro and in vivo M4 Positive Allosteric Modulator (PAM): NMS Competition at rM4 Vanderbilt Screening Center for GPCRs, Ion Channels and Transporters 05/29/11
aid1923 Discovery of a Highly Selective in vitro and in vivo M4 Positive Allosteric Modulator(PAM): Analog Potency Vanderbilt Screening Center for GPCRs, Ion Channels and Transporters 05/29/11
aid1767 Discovery of novel allosteric modulators of the M1 muscarinic receptor: Agonist NMS competition at M2 Vanderbilt Screening Center for GPCRs, Ion Channels and Transporters 05/29/11
aid1757 Discovery of novel allosteric modulators of the M1 muscarinic receptor: Agonist NMS competition at M4 Vanderbilt Screening Center for GPCRs, Ion Channels and Transporters 05/29/11
aid1690 Dose Response for ABC transporter inhibitors: specifically ABCG2 screen, ABCB1 counter-screen NMMLSC 05/29/11
aid1888 Dose respone, multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS16-Galphao. NMMLSC 05/29/11
aid1869 Dose respone, multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS8-Galphao. NMMLSC 05/29/11
aid1884 Dose response, multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS19-Galphao. NMMLSC 05/29/11
aid1871 Dose response, multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS7-Galphao. NMMLSC 05/29/11
aid1701 Fluorescence-based counterscreen assay for S1P4 agonists: Cell-based dose response high throughput screening assay to identify agonists of the Sphingosine 1-Phosphate Receptor 1 (S1P1) The Scripps Research Institute Molecular Screening Center 05/29/11
aid1966 HTS Dose response counterscreen for assays utilizing the enzyme, b-galactosidase Burnham Center for Chemical Genomics 05/29/11
aid1736 Identification of Novel Modulators of Cl- dependent Transport Process via HTS; Dose-dependent Assay with KCC2 Vanderbilt Screening Center for GPCRs, Ion Channels and Transporters 05/29/11
aid1913 Luminescence-based dose response biochemical high throughput screening assay for inhibitors of the Heat Shock Protein 90 (HSP90) The Scripps Research Institute Molecular Screening Center 05/29/11
aid1699 Luminescent counterscreen for inhibitors of the Janus kinase 2 mutant JAK2V617F: dose response cell-based high throughput screening assay for inhibitors of parental Ba/F3 cell viability. The Scripps Research Institute Molecular Screening Center 05/29/11
aid1769 Profiling Assay to determine GST-GSH interactions in multiplex bead-based assays NMMLSC 05/29/11
aid1890 QFRET-based dose response biochemical high throughput screening assay to identify inhibitors of the SARS coronavirus 3C-like Protease (3CLPro) The Scripps Research Institute Molecular Screening Center 05/29/11
aid1957 SAR VHR1 Fluorescent Assay for In Vitro dose response studies Burnham Center for Chemical Genomics 05/29/11
aid1958 SAR VHR1 absorbance Assay for In Vitro dose response studies. Burnham Center for Chemical Genomics 05/29/11
aid1941 SAR assay for compounds inhibiting TNAP in the absence of phosphate acceptor performed in a luminescent assay Burnham Center for Chemical Genomics 05/29/11
aid1627 Cathepsin L dose-response testing in the presence of cysteine PCMD 05/28/11
aid936 Concentration Response Redox Cycling H2O2 Generation assay, 1 mM DTT, to characterize small molecule inhibitors identified in the Polo box domain (PBD) of Plk1 Primary HTS. University of Pittsburgh Molecular Library Screening Center 05/28/11
aid1057 Concentration Response fluorescence polarization-based assay to test PMLSC Chemistry Core synthesized analogs of confirmed hits from the Polo box domain (PBD) of Plk1 Primary HTS. University of Pittsburgh Molecular Library Screening Center 05/28/11
aid1536 Confirmation of compounds inhibiting phosphomannose isomerase (PMI) via a fluorescence intensity assay using a high concentration of mannose 6-phosphate. Burnham Center for Chemical Genomics 05/28/11
aid1535 Confirmation of compounds inhibiting phosphomannose isomerase (PMI) via a fluorescence intensity assay. Burnham Center for Chemical Genomics 05/28/11
aid1514 Counter Screen using XIAP-Bir3 of the Chemical Antagonists of IAP-family anti-apoptotic proteins confirmation assay Burnham Center for Chemical Genomics 05/28/11
aid1655 Counter screen SAR assay for PMM2 inhibitors via a fluorescence intensity assay Burnham Center for Chemical Genomics 05/28/11
aid1528 Counterscreen assay for PERK inhibitors: Dose response cell-based high throughput screening assay to measure inhibition of PERK at 6 hours The Scripps Research Institute Molecular Screening Center 05/28/11
aid874 Counterscreen for S1P2 Agonists: Dose Response High Throughput Cell-Based Screen to Identify Activators of CRE-BLA: S1P2 Purchased Analogues The Scripps Research Institute Molecular Screening Center 05/28/11
aid856 Counterscreen for S1P2 Antagonists: Dose Response Cell-Based Screen to Identify Antagonists of CRE-BLA The Scripps Research Institute Molecular Screening Center 05/28/11
aid1470 Discovery of novel allosteric modulators of the M1 muscarinic receptor: Agonist NMS binding at M1 Vanderbilt Screening Center for GPCRs, Ion Channels and Transporters 05/28/11
aid1323 Dose response biochemical High Throughput Screening assay for agonists of the steroid receptor coactivator 2 (SRC-2) recruitment by the peroxisome proliferator-activated receptor gamma (PPARgamma) The Scripps Research Institute Molecular Screening Center 05/28/11
aid1331 Dose response biochemical High Throughput Screening assay for agonists of the steroid receptor coactivator 3 (SRC-3) recruitment by the peroxisome proliferator-activated receptor gamma (PPARgamma) The Scripps Research Institute Molecular Screening Center 05/28/11
aid1534 Dose response biochemical high throughput screening assay for inhibitors of the p97 ATPase The Scripps Research Institute Molecular Screening Center 05/28/11
aid1399 Dose response cell-based assay to measure STAT3 inhibition The Scripps Research Institute Molecular Screening Center 05/28/11
aid1518 Dose response cell-based high throughput screening assay for antagonists of the Sphingosine 1-Phosphate Receptor 3 (S1P3) The Scripps Research Institute Molecular Screening Center 05/28/11
aid1562 Dose response cell-based high-throughput screening assay for agonists of the transient receptor potential channel ML3 (TRPML3) The Scripps Research Institute Molecular Screening Center 05/28/11
aid1538 Dose response cell-based high-throughput screening assay for agonists of the transient receptor potential channel N1 (TRPN1) The Scripps Research Institute Molecular Screening Center 05/28/11
aid1522 Dose response cell-based high-throughput screening assay to measure PERK inhibition The Scripps Research Institute Molecular Screening Center 05/28/11
aid1411 Dose response counterscreen assay for STAT3 inhibitors: cell-based high throughput assay to measure STAT1 inhibition The Scripps Research Institute Molecular Screening Center 05/28/11
aid1409 Dose response counterscreen for STAT1 inhibitors: cell-based high throughput assay to measure STAT3 inhibition The Scripps Research Institute Molecular Screening Center 05/28/11
aid1221 Estrogen Receptor (beta) binding: Dose Response of Primary Screen Assay NMMLSC 05/28/11
aid1342 Fluorescence polarization assay for PKD inhibitiors-interference assay-57K HTS campaign University of Pittsburgh Molecular Library Screening Center 05/28/11
aid1077 Fluorescent secondary assay for dose-response confirmation of chemical inhibitors of HePTP Burnham Center for Chemical Genomics 05/28/11
aid1632 HTS assay for inhibitors of Trypanosoma brucei hexokinase 1: IC50 determinations University of Pittsburgh Molecular Library Screening Center 05/28/11
aid1193 In Vitro Hsc70 Dose Response Fluorescence Polarization Assay Sanford-Burnham Center for Chemical Genomics 05/28/11
aid1544 Luminescence counterscreen assay for p97 inhibitors: Dose response biochemical high throughput screening assay to identify inhibitors of the C522A mutant p97 ATPase. The Scripps Research Institute Molecular Screening Center 05/28/11
aid1629 Luminescence counterscreen assay for p97 inhibitors: dose response biochemical high throughput screening assay to identify inhibitors of the C522A mutant p97 ATPase: synthesized compounds. The Scripps Research Institute Molecular Screening Center 05/28/11
aid1512 Luminescent assay for HTS discovery of chemical inhibitors of placental alkaline phosphatase confirmation Burnham Center for Chemical Genomics 05/28/11
aid1330 Multiplexed dose response screen for small molecule regulators of Bcl-2 family protein interactions, specifically Bim-Bcl-W. NMMLSC 05/28/11
aid1340 Multiplexed dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Rac wildtype NMMLSC 05/28/11
aid1327 Multiplexed high-throughput screen for small molecule regulators of Bcl-2 family protein interactions, specifically Bim-Bcl-B protein. NMMLSC 05/28/11
aid1324 Profiling Assay to determine GST-GSH interactions in multiplex bead-based assays (HPSMTB buffer) NMMLSC 05/28/11
aid1056 SAR analysis of an In Vitro TNAP Dose Response Luminescent Assay Burnham Center for Chemical Genomics 05/28/11
aid1666 SAR assay for compounds that inhibit PHOSPHO1 Burnham Center for Chemical Genomics 05/28/11
aid1028 Screening for Inhibitors of the Mevalonate Pathway in Streptococcus Pneumoniae - DPM-DC - Secondary Assay SRMLSC 05/28/11
aid1641 TR-FRET counterscreen for FAK inhibitors: dose-response biochemical high throughput screening assay to identify inhibitors of Proline-rich tyrosine kinase 2 (Pyk2) The Scripps Research Institute Molecular Screening Center 05/28/11
aid689 Colorimetric assay for HTS discovery of chemical inhibitors of EphA4 receptor antagonists Sanford-Burnham Center for Chemical Genomics 05/27/11
aid779 Counter Screen for Placental Alkaline Phosphatase-based Assays Positives Burnham Center for Chemical Genomics 05/27/11
aid843 Counter screen for S1P2 Agonists: Dose Response High Throughput Cell-Based Screen to Identify Activators of CRE-BLA The Scripps Research Institute Molecular Screening Center 05/27/11
aid842 Dose response biochemical assay to identify inhibitors of the HIV Rev - RRE RNA interaction (disruption of protein-RNA interaction) The Scripps Research Institute Molecular Screening Center 05/27/11
aid852 Factor XIIa 1536 HTS Dose Response Confirmation PCMD 05/27/11
aid844 Identification of Molecular Probes that Activate MRP-1 - Dose Response SRMLSC 05/27/11
aid518 TNAP luminescent HTS assay Burnham Center for Chemical Genomics 05/27/11
aid1744 Discovery of novel allosteric modulators of the M1 muscarinic receptor: Agonist Activity against Muscarinic Panel Vanderbilt Screening Center for GPCRs, Ion Channels and Transporters 05/25/11
aid1734 Identification of Novel Modulators of Cl- dependent Transport Process via HTS: Rubidium Flux Vanderbilt Screening Center for GPCRs, Ion Channels and Transporters 05/25/11
aid1749 SAR analysis of Antagonists of IAP-family anti-apoptotic proteins Burnham Center for Chemical Genomics 05/25/11
aid1750 SAR analysis of Antagonists of XIAP-Bir3 domain of IAP-family anti-apoptotic proteins Burnham Center for Chemical Genomics 05/25/11
aid1755 SAR analysis of compounds that potentiate TRAIL-induced apoptosis in MDA-MB-435 cells. Burnham Center for Chemical Genomics 05/25/11
aid1752 SAR analysis of compounds that potentiate TRAIL-induced apoptosis in PPC-1 cells. Burnham Center for Chemical Genomics 05/25/11
aid1378 AKT counterscreen of confirmed PKD inhibitors-57K library University of Pittsburgh Molecular Library Screening Center 05/21/11
aid1380 CDK7 counterscreen of confirmed PKD inhibitors-57K library addition University of Pittsburgh Molecular Library Screening Center 05/21/11
aid1449 Chemical Antagonists of IAP-family anti-apoptotic proteins confirmation Burnham Center for Chemical Genomics 05/21/11
aid1414 Counterscreen assay for inhibitors of Wee1 degradation: dose response cell-based assay to identify inhibitors of cyclin B degradation The Scripps Research Institute Molecular Screening Center 05/21/11
aid1412 Dose Response Cell-based Assay for Inhibitors of Wee1 Degradation The Scripps Research Institute Molecular Screening Center 05/21/11
aid1396 Dose response cell-based assay to measure STAT1 inhibition The Scripps Research Institute Molecular Screening Center 05/21/11
aid1398 Dose response cell-based assay to measure STAT3 activation The Scripps Research Institute Molecular Screening Center 05/21/11
aid1406 Dose response counterscreen assay for STAT3 activators: cell-based high throughput assay to measure STAT1 activation The Scripps Research Institute Molecular Screening Center 05/21/11
aid1404 Dose response counterscreen for STAT1 activators: cell-based high throughput assay to measure STAT3 activation The Scripps Research Institute Molecular Screening Center 05/21/11
aid1394 E3 Ligase dose-response_384 PCMD 05/21/11
aid1383 PLK1 counterscreening assay for identified PKD inhibitors University of Pittsburgh Molecular Library Screening Center 05/21/11
aid1392 RNA polymerase SAR PCMD 05/21/11
aid1450 SAR assay for compounds activating TNAP in the absence of phosphate acceptor performed in a luminescent assay Burnham Center for Chemical Genomics 05/21/11
aid1319 Dose response biochemical High Throughput Screening assay for agonists of the steroid receptor coactivator 1 (SRC-1) recruitment by the peroxisome proliferator-activated receptor gamma (PPARgamma) The Scripps Research Institute Molecular Screening Center 05/20/11
aid1284 Dose response biochemical screening assay for inhibitors of c-Jun N-Terminal Kinase 3 (JNK3) The Scripps Research Institute Molecular Screening Center 05/20/11
aid1268 Dose response cell-based high throughput screening assay to identify enhancers of beta-glucosidase activity The Scripps Research Institute Molecular Screening Center 05/20/11
aid1277 Dose response cell-based screening assay for antagonists of neuropeptide Y receptor Y1 (NPY-Y1) The Scripps Research Institute Molecular Screening Center 05/20/11
aid1278 Dose response counterscreen assay for neuropeptide Y receptor Y1 (NPY-Y1): Cell-based high throughput assay to measure NPY-Y2 antagonism The Scripps Research Institute Molecular Screening Center 05/20/11
aid1279 Dose response counterscreen for neuropeptide Y receptor Y2 (NPY-Y2): Cell-based high throughput assay to measure NPY-Y1 antagonism The Scripps Research Institute Molecular Screening Center 05/20/11
aid1333 Multiplex dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Cdc42 activated mutant NMMLSC 05/20/11
aid1337 Multiplex dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Rab2 wildtype NMMLSC 05/20/11
aid1339 Multiplex dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Rac activated mutant NMMLSC 05/20/11
aid1329 Multiplexed dose response screen for small molecule regulators of Bcl-2 family protein interactions, specifically Bim-Mcl-1. NMMLSC 05/20/11
aid1335 Multiplexed dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Ras wildtype NMMLSC 05/20/11
aid1328 Multiplexed high-throughput screen for small molecule regulators of Bcl-2 family protein interactions, specifically Bim-Bcl-2 NMMLSC 05/20/11
aid1261 YopH - IC50 determinations (10 point dose range) University of Pittsburgh Molecular Library Screening Center 05/20/11
aid1003 Confirmation Cuvette-Based Assay for Inhibitors of AmpC Beta-Lactamase (assay with detergent) NCGC 05/17/11
aid1244 Counter Screen for TR3-Based Bcl-B Inhibitors: Fluorescence Polarization Bcl-B/FITC-Bim-BH3 Assay Sanford-Burnham Center for Chemical Genomics 05/17/11
aid1050 Dose Response cell-based high-throughput screening assay to identify agonists of galanin receptor 2 (GALR2) The Scripps Research Institute Molecular Screening Center 05/17/11
aid1225 Dose Response cell-based high-throughput screening assay to identify antagonists of galanin receptor 2 (GALR2) The Scripps Research Institute Molecular Screening Center 05/17/11
aid1228 Dose response counterscreen for agonists of galanin receptor 2 (GalR2): a cell-based high-throughput screening assay for activators of beta-lactamase activity The Scripps Research Institute Molecular Screening Center 05/17/11
aid1238 Dose response counterscreen for antagonists of galanin receptor 2 (GalR2): a cell-based high-throughput screening assay for inhibitors of beta-lactamase activity The Scripps Research Institute Molecular Screening Center 05/17/11
aid1223 Estrogen Receptor (alpha) binding: Dose Response of Primary Screen Assay NMMLSC 05/17/11
aid1079 Estrogen Receptor-alpha Coactivator Binding Inhibitors ELISA Secondary Assay Emory University Molecular Libraries Screening Center 05/17/11
aid1243 Fluorescence Polarization Dose Response Assay for TR3-Based Bcl-B Inhibitors Sanford-Burnham Center for Chemical Genomics 05/17/11
aid1227 GAPDH Dose Response Colorimetric Assay Sanford-Burnham Center for Chemical Genomics 05/17/11
aid1233 High Throughput Screen to Identify Compounds that Inhibit Class II HMG-CoA Reductases - Confirmatory Screen SRMLSC 05/17/11
aid1070 In Vitro Bfl-1 Dose Response Fluorescence Polarization Assay for SAR Study Sanford-Burnham Center for Chemical Genomics 05/17/11
aid1072 In Vitro Hsp70 Dose Response Fluorescence Polarization Assay for SAR Study Burnham Center for Chemical Genomics 05/17/11
aid1017 Luminescent assay for identification of inhibitors of human intestinal alkaline phosphatase Sanford-Burnham Center for Chemical Genomics 05/17/11
aid1052 MKP-3 in vitro secondary assay for identification of irreversible and slow-binding inhibitors Burnham Center for Chemical Genomics 05/17/11
aid1058 SMAD Transcription Factor Inhibitors Secondary Dose Response Confirmation Emory University Molecular Libraries Screening Center 05/17/11
aid1026 sEH_DR_Inh_Infinite200_Fluorescence_01072008 Columbia University Molecular Screening Center 05/17/11
aid832 Cathepsin G dose-response confirmation PCMD 05/12/11
aid831 Cathepsin S dose-response confirmation PCMD 05/12/11
aid876 Concentration Response Redox Cycling H2O2 Generation assay to characterize small molecule inhibitors identified in the Polo box domain (PBD) of Plk1 Primary HTS. University of Pittsburgh Molecular Library Screening Center 05/12/11
aid877 Concentration Response fluorescence polarization-based assay to confirm small molecule inhibitors identified in the Polo box domain (PBD) of Plk1 Primary HTS. University of Pittsburgh Molecular Library Screening Center 05/12/11
aid854 Dose Response Cell Based Assay for Agonists of the S1P2 Receptor The Scripps Research Institute Molecular Screening Center 05/12/11
aid872 Dose Response Cell Based Assay for Agonists of the S1P2 Receptor of Purchased Analogues The Scripps Research Institute Molecular Screening Center 05/12/11
aid851 Dose Response Cell Based Assay for Antagonists of the S1P2 Receptor The Scripps Research Institute Molecular Screening Center 05/12/11
aid835 Dose-response biochemical assay for antagonists of the interaction between the Eph receptor B4 (EphB4) and its ligand ephrin-B2 via TNYL-RAW peptide The Scripps Research Institute Molecular Screening Center 05/12/11
aid838 Mycobacterium tuberculosis Pantothenate Synthetase Secondary Assay SRMLSC 05/12/11
aid820 Cathepsin B dose-response confirmation PCMD 05/11/11
aid825 Cathepsin L dose-response confirmation PCMD 05/11/11
aid829 Complement C1s ELISA PCMD 05/11/11
aid787 Complement factor C1s IC50 from mixture screen PCMD 05/11/11
aid810 Dose-response biochemical assay for inhibitors of Focal Adhesion Kinase (FAK) The Scripps Research Institute Molecular Screening Center 05/11/11
aid826 RNA polymerase dose-response confirmation PCMD 05/11/11
aid786 TR-FRET secondary assay for HTS discovery of chemical inhibitors of Hsp70 Burnham Center for Chemical Genomics 05/11/11
aid714 BAP1 Enzyme inhibitors Dose Response Confirmation Emory University Molecular Libraries Screening Center 05/06/11
aid754 Cell-based secondary assay for identifying Hsp90 inhibitors that degrade Hsp90 client protein Her2 Emory University Molecular Libraries Screening Center 05/06/11
aid769 Dose response biochemical assay for autofluorescent inhibitors of Matrix Metalloproteinase 13 (MMP13) activity The Scripps Research Institute Molecular Screening Center 05/06/11
aid735 Dose-response biochemical assay for inhibitors of Matrix Metalloproteinase 13 (MMP13) activity The Scripps Research Institute Molecular Screening Center 05/06/11
aid713 Estrogen Receptor-alpha Coactivator Binding Inhibitors Dose Response Confirmation Emory University Molecular Libraries Screening Center 05/06/11
aid737 Estrogen Receptor-alpha Coactivator Binding Potentiators Dose Response Confirmation Emory University Molecular Libraries Screening Center 05/06/11
aid716 Factor XIIa Dose Response Confirmation PCMD 05/06/11
aid724 Formylpeptide Receptor (FPR) Ligand Structure Activity Relationship (SAR) Analysis : Dose Response Assay NMMLSC 05/06/11
aid723 Formylpeptide Receptor (FPR) Ligand Structure Activity Relationship (SAR) Analysis : Dose Response Assay Counterscreen Against Formyl Peptide Receptor-Like-1 (FPRL1) NMMLSC 05/06/11
aid766 Formylpeptide Receptor (FPRL1) Ligand Structure Activity Relationship (SAR) Analysis : Dose Response Assay NMMLSC 05/06/11
aid762 Formylpeptide Receptor (FPRL1) Ligand Structure Activity Relationship (SAR) Analysis : FPR Dose Response Counterscreen Assay NMMLSC 05/06/11
aid748 High Throughput Fluorescence Polarization Screen for Bcl-B Phenotype Converters Burnham Center for Chemical Genomics 05/06/11
aid730 S1P3 Dose Response Assay Counterscreen for 5-Hydroxytryptamine(Serotonin) Receptor Subtype 1E Agonists The Scripps Research Institute Molecular Screening Center 05/06/11
aid776 S1P3 Dose Response Assay Counterscreen for 5-Hydroxytryptamine(Serotonin) Receptor Subtype 1E Antagonists The Scripps Research Institute Molecular Screening Center 05/06/11
aid715 SMAD Transcription Factor Inhibitors Dose Response Confirmation Emory University Molecular Libraries Screening Center 05/06/11
aid711 14-3-3 protein interaction modulators Dose Response Confirmation Emory University Molecular Libraries Screening Center 05/05/11
aid695 Counterscreen for activators of the Retinoic Acid Receptor-related orphan receptor A (RORA): A cell-based dose-response assay for inhibition of the Steroidogenic Factor 1 (SF-1) The Scripps Research Institute Molecular Screening Center 05/04/11
aid692 Dose-response cell-based assay for activators of the nuclear receptor Steroidogenic Factor 1 (SF-1) The Scripps Research Institute Molecular Screening Center 05/04/11
aid569 Cdc25B Catalytic Domain Protein Tyrosine Phosphatase HTS Dose Response Confirmation Assay University of Pittsburgh Molecular Library Screening Center 04/30/11
aid650 Cdc25B Catalytic Domain Protein Tyrosine Phosphatase Probe Assessment Dose Response Reproducibility Assay University of Pittsburgh Molecular Library Screening Center 04/30/11
aid649 Cdc25B Catalytic Domain Protein Tyrosine Phosphatase Probe Assessment Dose Response assay in 25 mM DTT University of Pittsburgh Molecular Library Screening Center 04/30/11
aid669 Cdc25B Catalytic Domain Protein Tyrosine Phosphatase Probe Assessment Dose Response assay in 25 mM DTT and Catalase. University of Pittsburgh Molecular Library Screening Center 04/30/11
aid670 Cdc25B Catalytic Domain Protein Tyrosine Phosphatase Probe Assessment Dose Response assay in the presence of Beta-Mercaptoethanol. University of Pittsburgh Molecular Library Screening Center 04/30/11
aid668 Cdc25B Catalytic Domain Protein Tyrosine Phosphatase Probe Assessment Dose Response assay in the presence of Catalase. University of Pittsburgh Molecular Library Screening Center 04/30/11
aid671 Cdc25B Catalytic Domain Protein Tyrosine Phosphatase Probe Assessment Dose Response assay in the presence of Glutathione. University of Pittsburgh Molecular Library Screening Center 04/30/11
aid674 Cdc25B Catalytic Domain Protein Tyrosine Phosphatase Probe Assessment: MKP-1 Dose Response Selectivity comparison. University of Pittsburgh Molecular Library Screening Center 04/30/11
aid673 Cdc25B Catalytic Domain Protein Tyrosine Phosphatase Probe Assessment: MKP-3 Dose Response Selectivity comparison. University of Pittsburgh Molecular Library Screening Center 04/30/11
aid675 Counterscreen for activators of the nuclear receptor Steroidogenic Factor 1 (SF-1): A cell-based dose-response assay for inhibition of the RAR-related orphan receptor A (RORA) The Scripps Research Institute Molecular Screening Center 04/30/11
aid611 Counterscreen for inhibitors of the Retinoic Acid Receptor-related orphan receptor A (RORA): A cell-based dose-response assay for inhibition of the Steroidogenic Factor 1 (SF-1) The Scripps Research Institute Molecular Screening Center 04/30/11
aid599 Counterscreen for inhibitors of the nuclear receptor Steroidogenic Factor 1 (SF-1): A cell-based dose-response assay for inhibition of the RAR-related orphan receptor A (RORA) The Scripps Research Institute Molecular Screening Center 04/30/11
aid644 Dose-response biochemical assay of inhibitors of Rho kinase 2 (Rock2) The Scripps Research Institute Molecular Screening Center 04/30/11
aid681 Dose-response cell-based assay for activators of the Retinoic Acid Receptor-related orphan receptor A (RORA) The Scripps Research Institute Molecular Screening Center 04/30/11
aid610 Dose-response cell-based assay for inhibitors of the Retinoic Acid Receptor-related orphan receptor A (RORA) The Scripps Research Institute Molecular Screening Center 04/30/11
aid600 Dose-response cell-based assay for inhibitors of the nuclear receptor Steroidogenic Factor 1 (SF-1) The Scripps Research Institute Molecular Screening Center 04/30/11
aid679 Factor XIa Dose Response Confirmation PCMD 04/30/11
aid606 HTS for LYP Inhibitors-an Autoimmunity Target - Primary screen Columbia University Molecular Screening Center 04/30/11
aid562 In vitro MKP-1 Phosphatase Dose Response Active/Probe Assessment Assay - Effects of Catalase University of Pittsburgh Molecular Library Screening Center 04/30/11
aid558 In vitro MKP-1 Phosphatase Dose Response Active/Probe Assessment Assay - Effects of DTT University of Pittsburgh Molecular Library Screening Center 04/30/11
aid563 In vitro MKP-1 Phosphatase Dose Response Active/Probe Assessment Assay - Reproducibility testing University of Pittsburgh Molecular Library Screening Center 04/30/11
aid564 In vitro MKP-3 Phosphatase Dose Response Active/Probe Assessment Assay - Effects of Catalase University of Pittsburgh Molecular Library Screening Center 04/30/11
aid566 In vitro MKP-3 Phosphatase Dose Response Active/Probe Assessment Assay - Reproducibility testing University of Pittsburgh Molecular Library Screening Center 04/30/11
aid690 Luminescent assay for HTS discovery of chemical inhibitors of placental alkaline phosphatase Burnham Center for Chemical Genomics 04/30/11
aid676 MKP-1 Dual Specificity Protein Tyrosine Phosphatase Probe Assessment: Cdc25B Dose Response Selectivity Assay University of Pittsburgh Molecular Library Screening Center 04/30/11
aid557 Screening for Inhibitors of the Mevalonate Pathway in Streptococcus Pneumoniae - MK Dose Response SRMLSC 04/30/11
aid621 TR-FRET secondary assay for HTS discovery of chemical inhibitors of anti-apoptotic protein Bfl-1 Sanford-Burnham Center for Chemical Genomics 04/30/11
aid653 West Nile Virus NS2bNS3 Proteinase Inhibitor Dose Response Confirmation. University of Pittsburgh Molecular Library Screening Center 04/30/11
aid523 Cathepsin B Inhibitor Series SAR Study PCMD 04/29/11
aid486 Clearance of Mutant Huntingtin Protein - Confirmatory screen Columbia University Molecular Screening Center 04/29/11
aid519 Dose Response Assay for Formylpeptide Receptor (FPR) Ligands and Dose Response Counter-Screen Assay for Formylpeptide-Like-1 (FPRL1) Ligands NMMLSC 04/29/11
aid520 Dose Response Assay for Formylpeptide Receptor-Like-1 (FPRL1) Ligands and Dose Response Counter-Screen Assay for Formylpeptide Receptor (FPR) Ligands NMMLSC 04/29/11
aid484 Dose Response Assay for S1P3 Antagonists The Scripps Research Institute Molecular Screening Center 04/29/11
aid468 Dose Response Assays for S1P1 Agonists and Agonism Potentiators - Agonist Assay 60K MLSMR The Scripps Research Institute Molecular Screening Center 04/29/11
aid548 Dose-response biochemical assay for inhibitors of protein kinase A (PKA) activity The Scripps Research Institute Molecular Screening Center 04/29/11
aid553 In vitro MKP-3 Phosphatase Dose Response Hit/Probe Assessment Assay University of Pittsburgh Molecular Library Screening Center 04/29/11
aid550 Screening for Inhibitors of the Mevalonate Pathway in Streptococcus Pneumoniae - DPM-DC Dose Response SRMLSC 04/29/11
aid549 Screening for Inhibitors of the Mevalonate Pathway in Streptococcus Pneumoniae - PMK Dose Response SRMLSC 04/29/11
aid443 Cdc25B Catalytic Domain Protein Tyrosine Phosphatase Dose Response Confirmation and Secondary Selectivity/Specificity Assay University of Pittsburgh Molecular Library Screening Center 04/28/11
aid467 Dose Response Assays for S1P1 Agonists and Agonism Potentiators - Parental Cell Line Counter Screen 60K MLSMR The Scripps Research Institute Molecular Screening Center 04/28/11
aid466 Dose Response Assays for S1P1 Agonists and Agonism Potentiators - Potentiator Assay 60K MLSMR The Scripps Research Institute Molecular Screening Center 04/28/11
aid442 In vitro MKP-1 Phosphatase Dose Response Confirmation and Secondary Selectivity/Specificity Assay University of Pittsburgh Molecular Library Screening Center 04/28/11
aid452 In vitro MKP-3 Phosphatase Dose Response Confirmation and Secondary Selectivity/Selectivity Assay University of Pittsburgh Molecular Library Screening Center 04/28/11
aid375 Mycobacterium tuberculosis Pantothenate Synthetase Assay SRMLSC 04/28/11
aid439 S1P3 Agonist Dose-Response Potency Assay The Scripps Research Institute Molecular Screening Center 04/28/11
aid1433 Kinase Inhibitor Selectivity Profiling Assay Ambit Biosciences 04/23/11
aid830 Cathepsin B mixture HTS dose-response confirmation PCMD 12/17/09
aid579 In vitro MKP-1 Phosphatase Dose Response SAR Support Assay CC_PMLSC 12/17/09
aid551 In vitro MKP-1 Phosphatase HTS Dose Response Confirmation Assay University of Pittsburgh Molecular Library Screening Center 12/17/09
aid652 HIV-1 RT-RNase H MLSCN MH077605 Probe Assessment: Dose response Assay University of Pittsburgh Molecular Library Screening Center 11/24/09
aid432 HTS discovery of chemical inhibitors of anti-apoptotic protein Bfl-1 Burnham Center for Chemical Genomics 11/24/09
aid1220 HTS identification of compounds inhibiting phosphomannose isomerase (PMI) via a fluorescence intensity assay using a high concentration of mannose 6-phosphate Burnham Center for Chemical Genomics 11/24/09
aid728 Factor XIIa Dose Response Confirmation from Single Well HTS PCMD 11/09/09
aid1215 Thrombin 1536 HTS Dose Response Confirmation PCMD 11/09/09
aid846 Factor XIa 1536 HTS Dose Response Confirmation PCMD 10/26/09
aid721 Factor XIa Dose Response Confirmation from Single Well Screen PCMD 10/26/09
aid1320 Multiplexed dose response screen for small molecule regulators of Bcl-2 family protein interactions, specifically Bim-Bfl-1. NMMLSC 10/26/09
aid1408 Fluorescence polarization assay for PKD inhibitiors-IC50 determinations University of Pittsburgh Molecular Library Screening Center 10/09/09
aid1322 Multiplexed dose response screen for small molecule regulators of Bcl-2 family protein interactions, specifically Bim-Bcl-XL. NMMLSC 10/09/09
aid712 Tumor Hsp90 Inhibitors Dose Response Confirmation Emory University Molecular Libraries Screening Center 10/09/09
aid583 High Throughput Screening Assay for Hsp70 Inhibitors Burnham Center for Chemical Genomics 09/25/09
aid1055 In Vitro MKP-3 Dose Response Assay for SAR Study Burnham Center for Chemical Genomics 09/25/09
aid1516 Counterscreen assay for S1P3 antagonists: Dose response cell-based high throughput screening assay to identify antagonists of the 5-Hydroxytryptamine Receptor Subtype 1E (5HT1E) The Scripps Research Institute Molecular Screening Center 09/05/09
aid749 Dose Response Cell Based Assay for Antagonists of the 5-Hydroxytryptamine Receptor Subtype 1E (5HT1E) The Scripps Research Institute Molecular Screening Center 09/05/09
aid726 Dose Response Cell Based High Throughput Screening Assay for Agonists of the 5-Hydroxytryptamine Receptor Subtype 1E (5HT1E) The Scripps Research Institute Molecular Screening Center 09/05/09
aid613 Dose Response Assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) Agonists The Scripps Research Institute Molecular Screening Center 08/14/09
aid755 Dose Response Cell Based Assay for Antagonists of the 5-Hydroxytryptamine Receptor Subtype 1A (5HT1A) The Scripps Research Institute Molecular Screening Center 08/14/09
aid718 Dose Response assay for agonists of 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1A (5HT1A) The Scripps Research Institute Molecular Screening Center 08/14/09
aid1560 Confirmation of compounds inhibiting the binding between the RUNX1 Runt domain and CBFb-SMMHC via a fluorescence resonance energy transfer (FRET) assay Burnham Center for Chemical Genomics 07/24/09
aid1550 Confirmation of compounds inhibiting the binding between the RUNX1 Runt domain and CBFbeta-SMMHC via a time resolved fluorescence resonance energy transfer (TR-FRET) assay. Burnham Center for Chemical Genomics 07/24/09
aid1434 uHTS identification of compounds inhibiting the binding between the RUNX1 Runt domain and CBFbeta-SMMHC via a fluorescence resonance energy transfer (FRET) assay. Burnham Center for Chemical Genomics 07/24/09
aid1438 Identification of compounds inhibiting the binding between the RUNX1 Runt domain and CBFb-SMMHC via a time resolved fluorescence resonance energy transfer (TR-FRET) assay. Burnham Center for Chemical Genomics 06/18/09