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Found 101 with Last Name = 'warner' and Initial = 'i'
TargetPeptide deformylase(Staphylococcus aureus (strain Mu50 / ATCC 700699))
Genomics Institute Of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50224039(CHEMBL36605)
Affinity DataIC50: <5nMAssay Description:Inhibitory activity towards Ni-peptide deformylase of Staphylococcus aureusMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptide deformylase(Staphylococcus aureus (strain Mu50 / ATCC 700699))
Genomics Institute Of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50224041(CHEMBL34538)
Affinity DataIC50: <5nMAssay Description:Inhibitory activity towards Ni-peptide deformylase of Staphylococcus aureusMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptide deformylase(Staphylococcus aureus (strain Mu50 / ATCC 700699))
Genomics Institute Of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50224038(CHEMBL38016)
Affinity DataIC50: <5nMAssay Description:Inhibitory activity towards Ni-peptide deformylase of Staphylococcus aureusMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptide deformylase(Staphylococcus aureus (strain Mu50 / ATCC 700699))
Genomics Institute Of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50224040(CHEMBL286441)
Affinity DataIC50: <5nMAssay Description:Inhibitory activity towards Ni-peptide deformylase of Staphylococcus aureusMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptide deformylase(Staphylococcus aureus (strain Mu50 / ATCC 700699))
Genomics Institute Of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50224042(CHEMBL36140)
Affinity DataIC50: <5nMAssay Description:Inhibitory activity towards Ni-peptide deformylase of Staphylococcus aureusMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptide deformylase(Staphylococcus aureus (strain Mu50 / ATCC 700699))
Genomics Institute Of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50141373(CHEMBL37719 | N-Hydroxy-2-(3-oxo-3,4-dihydro-2H-be...)
Affinity DataIC50: <5nMAssay Description:Inhibitory activity towards Ni-peptide deformylase of Staphylococcus aureusMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptide deformylase(Staphylococcus aureus (strain Mu50 / ATCC 700699))
Genomics Institute Of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50224043(CHEMBL36229)
Affinity DataIC50: <5nMAssay Description:Inhibitory activity towards Ni-peptide deformylase of Staphylococcus aureusMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptide deformylase(Staphylococcus aureus (strain Mu50 / ATCC 700699))
Genomics Institute Of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50089194((R)-N*4*-Hydroxy-N*1*-[(S)-1-((S)-2-hydroxymethyl-...)
Affinity DataIC50: <5nMAssay Description:Inhibitory activity towards Ni-peptide deformylase of Staphylococcus aureusMore data for this Ligand-Target Pair
TargetPeptide deformylase(Staphylococcus aureus (strain Mu50 / ATCC 700699))
Genomics Institute Of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50141359(CHEMBL285938 | N-Hydroxy-N-(3-oxo-3,4-dihydro-2H-b...)
Affinity DataIC50:  10nMAssay Description:Inhibitory activity towards Ni-peptide deformylase of Staphylococcus aureusMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptide deformylase(Staphylococcus aureus (strain Mu50 / ATCC 700699))
Genomics Institute Of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50141360(2-(4-Benzyl-3-oxo-3,4-dihydro-2H-benzo[1,4]thiazin...)
Affinity DataIC50:  12nMAssay Description:Inhibitory activity towards Ni-peptide deformylase of Staphylococcus aureusMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptide deformylase(Staphylococcus aureus (strain Mu50 / ATCC 700699))
Genomics Institute Of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50141370(CHEMBL34024 | N-Hydroxy-2-[3-oxo-4-(tetrahydro-pyr...)
Affinity DataIC50:  18nMAssay Description:Inhibitory activity towards Ni-peptide deformylase of Staphylococcus aureusMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptide deformylase(Staphylococcus aureus (strain Mu50 / ATCC 700699))
Genomics Institute Of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50141369(2-(4-Cyclopropylmethyl-3-oxo-3,4-dihydro-2H-benzo[...)
Affinity DataIC50:  29nMAssay Description:Inhibitory activity towards Ni-peptide deformylase of Staphylococcus aureusMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptide deformylase(Staphylococcus aureus (strain Mu50 / ATCC 700699))
Genomics Institute Of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50141363(CHEMBL287497 | N-Hydroxy-2-(4-methyl-3-oxo-3,4-dih...)
Affinity DataIC50:  37nMAssay Description:Inhibitory activity towards Ni-peptide deformylase of Staphylococcus aureusMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptide deformylase(Staphylococcus aureus (strain Mu50 / ATCC 700699))
Genomics Institute Of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50141365(2-(4-Cyclobutylmethyl-3-oxo-3,4-dihydro-2H-benzo[1...)
Affinity DataIC50:  41nMAssay Description:Inhibitory activity towards Ni-peptide deformylase of Staphylococcus aureusMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptide deformylase(Staphylococcus aureus (strain Mu50 / ATCC 700699))
Genomics Institute Of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50141366(2-(2-Hydroxycarbamoylmethyl-3-oxo-2,3-dihydro-benz...)
Affinity DataIC50:  44nMAssay Description:Inhibitory activity towards Ni-peptide deformylase of Staphylococcus aureusMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptide deformylase(Staphylococcus aureus (strain Mu50 / ATCC 700699))
Genomics Institute Of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50141385(2-[4-(3,3-Dimethyl-2-oxo-butyl)-3-oxo-3,4-dihydro-...)
Affinity DataIC50:  50nMAssay Description:Inhibitory activity towards Ni-peptide deformylase of Staphylococcus aureusMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptide deformylase(Staphylococcus aureus (strain Mu50 / ATCC 700699))
Genomics Institute Of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50141390(2-[4-(2-Cyclohexyl-ethyl)-3-oxo-3,4-dihydro-2H-ben...)
Affinity DataIC50:  57nMAssay Description:Inhibitory activity towards Ni-peptide deformylase of Staphylococcus aureusMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptide deformylase(Staphylococcus aureus (strain Mu50 / ATCC 700699))
Genomics Institute Of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50141374(2-{4-[(2,5-Difluoro-phenylcarbamoyl)-methyl]-3-oxo...)
Affinity DataIC50:  58nMAssay Description:Inhibitory activity towards Ni-peptide deformylase of Staphylococcus aureusMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptide deformylase(Staphylococcus aureus (strain Mu50 / ATCC 700699))
Genomics Institute Of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50141388(CHEMBL34426 | N-Hydroxy-2-[1-(3-methyl-butyl)-2-ox...)
Affinity DataIC50:  63nMAssay Description:Inhibitory activity towards Ni-peptide deformylase of Staphylococcus aureusMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptide deformylase(Staphylococcus aureus (strain Mu50 / ATCC 700699))
Genomics Institute Of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50141389(CHEMBL37522 | N-Hydroxy-2-(2-oxo-1,2,3,4-tetrahydr...)
Affinity DataIC50:  73nMAssay Description:Inhibitory activity towards Ni-peptide deformylase of Staphylococcus aureusMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptide deformylase(Staphylococcus aureus (strain Mu50 / ATCC 700699))
Genomics Institute Of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50141376(2-(8-Bromo-3-oxo-3,4-dihydro-2H-benzo[1,4]thiazin-...)
Affinity DataIC50:  74nMAssay Description:Inhibitory activity towards Ni-peptide deformylase of Staphylococcus aureusMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptide deformylase(Staphylococcus aureus (strain Mu50 / ATCC 700699))
Genomics Institute Of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50141368(CHEMBL38164 | N-Methoxy-2-(3-oxo-3,4-dihydro-2H-be...)
Affinity DataIC50:  74nMAssay Description:Inhibitory activity towards Ni-peptide deformylase of Staphylococcus aureusMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target11-beta-hydroxysteroid dehydrogenase 1(Homo sapiens (Human))
University Of Edinburgh

Curated by ChEMBL
LigandPNGBDBM50319324(1-(3,4-dimethoxyphenyl)-2-(1-m-tolyl-1H-tetrazol-5...)
Affinity DataIC50:  93nMAssay Description:Inhibition of human 11beta-HSD1 expressed in HEK293 cells by scintillation proximity assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target11-beta-hydroxysteroid dehydrogenase 1(Homo sapiens (Human))
University Of Edinburgh

Curated by ChEMBL
LigandPNGBDBM50319333(3-(1-(3-chlorophenyl)-1H-tetrazol-5-yl)-1-phenylpr...)
Affinity DataIC50:  114nMAssay Description:Inhibition of human 11beta-HSD1 expressed in HEK293 cells by scintillation proximity assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target11-beta-hydroxysteroid dehydrogenase 1(Homo sapiens (Human))
University Of Edinburgh

Curated by ChEMBL
LigandPNGBDBM50319316(1-(3,4-dimethoxyphenyl)-2-(1-phenyl-1H-tetrazol-5-...)
Affinity DataIC50:  116nMAssay Description:Inhibition of human 11beta-HSD1 expressed in HEK293 cells by scintillation proximity assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptide deformylase(Staphylococcus aureus (strain Mu50 / ATCC 700699))
Genomics Institute Of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50141392(2-(2-Hydroxycarbamoylmethyl-3-oxo-2,3-dihydro-benz...)
Affinity DataIC50:  168nMAssay Description:Inhibitory activity towards Ni-peptide deformylase of Staphylococcus aureusMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptide deformylase(Staphylococcus aureus (strain Mu50 / ATCC 700699))
Genomics Institute Of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50141364(CHEMBL284794 | N-hydroxy-2-(2-oxo-2,3-dihydro-1H-1...)
Affinity DataIC50:  169nMAssay Description:Inhibitory activity towards Ni-peptide deformylase of Staphylococcus aureusMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptide deformylase(Staphylococcus aureus (strain Mu50 / ATCC 700699))
Genomics Institute Of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50141387(2-(1-Cyclopropylmethyl-2-oxo-1,2,3,4-tetrahydro-qu...)
Affinity DataIC50:  175nMAssay Description:Inhibitory activity towards Ni-peptide deformylase of Staphylococcus aureusMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target11-beta-hydroxysteroid dehydrogenase 1(Homo sapiens (Human))
University Of Edinburgh

Curated by ChEMBL
LigandPNGBDBM50319331(2-(1-cyclohexyl-1H-tetrazol-5-ylthio)-1-(3,4-dimet...)
Affinity DataIC50:  183nMAssay Description:Inhibition of human 11beta-HSD1 expressed in HEK293 cells by scintillation proximity assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target11-beta-hydroxysteroid dehydrogenase 1(Homo sapiens (Human))
University Of Edinburgh

Curated by ChEMBL
LigandPNGBDBM50319360(1-(3-methoxyphenyl)-3-(1-phenyl-1H-tetrazol-5-yl)p...)
Affinity DataIC50:  215nMAssay Description:Inhibition of human 11beta-HSD1 expressed in HEK293 cells by scintillation proximity assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptide deformylase(Staphylococcus aureus (strain Mu50 / ATCC 700699))
Genomics Institute Of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50141382(CHEMBL287247 | N-Benzyloxy-2-(3-oxo-3,4-dihydro-2H...)
Affinity DataIC50:  230nMAssay Description:Inhibitory activity towards Ni-peptide deformylase of Staphylococcus aureusMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target11-beta-hydroxysteroid dehydrogenase 1(Homo sapiens (Human))
University Of Edinburgh

Curated by ChEMBL
LigandPNGBDBM50319310(3,3-dimethyl-1-(1-phenyl-1H-tetrazol-5-ylthio)buta...)
Affinity DataIC50:  252nMAssay Description:Inhibition of human 11beta-HSD1 expressed in HEK293 cells by scintillation proximity assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target11-beta-hydroxysteroid dehydrogenase 1(Homo sapiens (Human))
University Of Edinburgh

Curated by ChEMBL
LigandPNGBDBM50319311(1-phenyl-2-(1-phenyl-1H-tetrazol-5-ylthio)ethanone...)
Affinity DataIC50:  257nMAssay Description:Inhibition of human 11beta-HSD1 expressed in HEK293 cells by scintillation proximity assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target11-beta-hydroxysteroid dehydrogenase 1(Homo sapiens (Human))
University Of Edinburgh

Curated by ChEMBL
LigandPNGBDBM50319317(1-phenyl-3-(1-phenyl-1H-tetrazol-5-ylthio)propan-2...)
Affinity DataIC50:  289nMAssay Description:Inhibition of human 11beta-HSD1 expressed in HEK293 cells by scintillation proximity assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptide deformylase(Staphylococcus aureus (strain Mu50 / ATCC 700699))
Genomics Institute Of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50141362(2-(4-Cyclohexylmethyl-3-oxo-3,4-dihydro-2H-benzo[1...)
Affinity DataIC50:  302nMAssay Description:Inhibitory activity towards Ni-peptide deformylase of Staphylococcus aureusMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target11-beta-hydroxysteroid dehydrogenase 1(Homo sapiens (Human))
University Of Edinburgh

Curated by ChEMBL
LigandPNGBDBM50319343(3-(1-(3-methoxyphenyl)-1H-tetrazol-5-yl)-1-phenylp...)
Affinity DataIC50:  304nMAssay Description:Inhibition of human 11beta-HSD1 expressed in HEK293 cells by scintillation proximity assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target11-beta-hydroxysteroid dehydrogenase 1(Homo sapiens (Human))
University Of Edinburgh

Curated by ChEMBL
LigandPNGBDBM50319358(1-(3-chlorophenyl)-3-(1-phenyl-1H-tetrazol-5-yl)pr...)
Affinity DataIC50:  310nMAssay Description:Inhibition of human 11beta-HSD1 expressed in HEK293 cells by scintillation proximity assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptide deformylase(Staphylococcus aureus (strain Mu50 / ATCC 700699))
Genomics Institute Of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50141379((3-Oxo-3,4-dihydro-2H-benzo[1,4]thiazin-2-yl)-acet...)
Affinity DataIC50:  330nMAssay Description:Inhibitory activity towards Ni-peptide deformylase of Staphylococcus aureusMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptide deformylase(Staphylococcus aureus (strain Mu50 / ATCC 700699))
Genomics Institute Of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50141372(CHEMBL417683 | N-Hydroxy-2-[3-oxo-4-(pyridin-2-ylc...)
Affinity DataIC50:  343nMAssay Description:Inhibitory activity towards Ni-peptide deformylase of Staphylococcus aureusMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target11-beta-hydroxysteroid dehydrogenase 1(Homo sapiens (Human))
University Of Edinburgh

Curated by ChEMBL
LigandPNGBDBM50319341(1-phenyl-3-(1-phenyl-1H-tetrazol-5-yl)propan-1-one...)
Affinity DataIC50:  359nMAssay Description:Inhibition of human 11beta-HSD1 expressed in HEK293 cells by scintillation proximity assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptide deformylase(Staphylococcus aureus (strain Mu50 / ATCC 700699))
Genomics Institute Of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50141358(CHEMBL285024 | N-Hydroxy-2-[3-oxo-4-(2-oxo-2-pyrro...)
Affinity DataIC50:  397nMAssay Description:Inhibitory activity towards Ni-peptide deformylase of Staphylococcus aureusMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target11-beta-hydroxysteroid dehydrogenase 1(Homo sapiens (Human))
University Of Edinburgh

Curated by ChEMBL
LigandPNGBDBM50319344(3-(1-(4-methoxyphenyl)-1H-tetrazol-5-yl)-1-phenylp...)
Affinity DataIC50:  426nMAssay Description:Inhibition of human 11beta-HSD1 expressed in HEK293 cells by scintillation proximity assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptide deformylase(Staphylococcus aureus (strain Mu50 / ATCC 700699))
Genomics Institute Of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50141371(CHEMBL36126 | N-Hydroxy-N-(3-oxo-3,4-dihydro-2H-be...)
Affinity DataIC50:  427nMAssay Description:Inhibitory activity towards Ni-peptide deformylase of Staphylococcus aureusMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target11-beta-hydroxysteroid dehydrogenase 1(Homo sapiens (Human))
University Of Edinburgh

Curated by ChEMBL
LigandPNGBDBM50319318(1-(furan-2-yl)-2-(1-phenyl-1H-tetrazol-5-ylthio)et...)
Affinity DataIC50:  485nMAssay Description:Inhibition of human 11beta-HSD1 expressed in HEK293 cells by scintillation proximity assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target11-beta-hydroxysteroid dehydrogenase 1(Homo sapiens (Human))
University Of Edinburgh

Curated by ChEMBL
LigandPNGBDBM50319365(3-(5-(4-methoxyphenyl)-1H-tetrazol-1-yl)-1-phenylp...)
Affinity DataIC50:  493nMAssay Description:Inhibition of human 11beta-HSD1 expressed in HEK293 cells by scintillation proximity assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target11-beta-hydroxysteroid dehydrogenase 1(Homo sapiens (Human))
University Of Edinburgh

Curated by ChEMBL
LigandPNGBDBM50319362(1-cyclohexyl-3-(1-phenyl-1H-tetrazol-5-yl)propan-1...)
Affinity DataIC50:  506nMAssay Description:Inhibition of human 11beta-HSD1 expressed in HEK293 cells by scintillation proximity assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptide deformylase(Staphylococcus aureus (strain Mu50 / ATCC 700699))
Genomics Institute Of The Novartis Research Foundation

Curated by ChEMBL
LigandPNGBDBM50141377(2-(4-Cyanomethyl-3-oxo-3,4-dihydro-2H-benzo[1,4]th...)
Affinity DataIC50:  515nMAssay Description:Inhibitory activity towards Ni-peptide deformylase of Staphylococcus aureusMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target11-beta-hydroxysteroid dehydrogenase 1(Homo sapiens (Human))
University Of Edinburgh

Curated by ChEMBL
LigandPNGBDBM50319359(1-(4-dichlorophenyl)-3-(1-phenyl-1H-tetrazol-5-yl)...)
Affinity DataIC50:  539nMAssay Description:Inhibition of human 11beta-HSD1 expressed in HEK293 cells by scintillation proximity assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target11-beta-hydroxysteroid dehydrogenase 1(Homo sapiens (Human))
University Of Edinburgh

Curated by ChEMBL
LigandPNGBDBM50319332(3-(1-(4-chlorophenyl)-1H-tetrazol-5-yl)-1-phenylpr...)
Affinity DataIC50:  575nMAssay Description:Inhibition of human 11beta-HSD1 expressed in HEK293 cells by scintillation proximity assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target11-beta-hydroxysteroid dehydrogenase 1(Homo sapiens (Human))
University Of Edinburgh

Curated by ChEMBL
LigandPNGBDBM50319334(1-phenyl-3-(1-p-tolyl-1H-tetrazol-5-yl)propan-1-on...)
Affinity DataIC50:  588nMAssay Description:Inhibition of human 11beta-HSD1 expressed in HEK293 cells by scintillation proximity assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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