Compile Data Set for Download or QSAR
maximum 50k data
Found 181 with Last Name = 'seth' and Initial = 'p'
TargetSigma non-opioid intracellular receptor 1(Homo sapiens (Human))
Medical College of Georgia

Curated by PDSP Ki Database
LigandPNGBDBM21398(4-[4-(4-Chloro-phenyl)-4-hydroxy-piperidin-1-yl]-1...)
Affinity DataKi:  3.70nMMore data for this Ligand-Target Pair
TargetSigma non-opioid intracellular receptor 1(Homo sapiens (Human))
Medical College of Georgia

Curated by PDSP Ki Database
LigandPNGBDBM85392(CAS_131443 | NSC_131443 | PPAP, (-))
Affinity DataKi:  7.30nMMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetSigma non-opioid intracellular receptor 1(Homo sapiens (Human))
Medical College of Georgia

Curated by PDSP Ki Database
LigandPNGBDBM15581(CHEMBL8706 | CLG | CLORGILINE | Clorgyline | N-[3-...)
Affinity DataKi:  8.70nMMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetSigma non-opioid intracellular receptor 1(Homo sapiens (Human))
Medical College of Georgia

Curated by PDSP Ki Database
LigandPNGBDBM94507(2-[2-(diethylamino)ethoxy]ethyl 1-phenylcyclopenta...)
Affinity DataKi:  10.4nMMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetSigma non-opioid intracellular receptor 1(Homo sapiens (Human))
Medical College of Georgia

Curated by PDSP Ki Database
LigandPNGBDBM85391(CAS_85976-54-1 | NSC_149136 | PPP, (+))
Affinity DataKi:  42nMMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetSigma non-opioid intracellular receptor 1(Homo sapiens (Human))
Medical College of Georgia

Curated by PDSP Ki Database
LigandPNGBDBM81982(CAS_97-39-2 | DITOLYLGUANIDINE | DTG | Di-o-tolylg...)
Affinity DataKi:  104nMMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetSigma non-opioid intracellular receptor 1(Homo sapiens (Human))
Medical College of Georgia

Curated by PDSP Ki Database
LigandPNGBDBM21397(8-[4-(4-fluorophenyl)-4-keto-butyl]-1-phenyl-1,3,8...)
Affinity DataKi:  353nMMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetSigma non-opioid intracellular receptor 1(Homo sapiens (Human))
Medical College of Georgia

Curated by PDSP Ki Database
LigandPNGBDBM50003560(4-methoxy-17-methyl-17-azatetracyclo[7.5.3.01,10.0...)
Affinity DataKi:  521nMMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetAcetylcholinesterase(Electrophorus electricus (Electric eel))
Jamia Millia Islamia (Central University)

Curated by ChEMBL
LigandPNGBDBM50524452(CHEMBL4451095)
Affinity DataIC50:  4.80nMAssay Description:Inhibition of electric eel AChE using acetylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition measured after 5 m...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Electrophorus electricus (Electric eel))
Jamia Millia Islamia (Central University)

Curated by ChEMBL
LigandPNGBDBM50524455(CHEMBL4560049)
Affinity DataIC50:  4.90nMAssay Description:Inhibition of electric eel AChE using acetylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition measured after 5 m...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Electrophorus electricus (Electric eel))
Jamia Millia Islamia (Central University)

Curated by ChEMBL
LigandPNGBDBM50524460(CHEMBL4437847)
Affinity DataIC50:  12nMAssay Description:Inhibition of electric eel AChE using acetylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition measured after 5 m...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Electrophorus electricus (Electric eel))
Jamia Millia Islamia (Central University)

Curated by ChEMBL
LigandPNGBDBM50524454(CHEMBL4474224)
Affinity DataIC50:  22nMAssay Description:Inhibition of electric eel AChE using acetylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition measured after 5 m...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Electrophorus electricus (Electric eel))
Jamia Millia Islamia (Central University)

Curated by ChEMBL
LigandPNGBDBM50524456(CHEMBL4444093)
Affinity DataIC50:  45nMAssay Description:Inhibition of electric eel AChE using acetylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition measured after 5 m...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Electrophorus electricus (Electric eel))
Jamia Millia Islamia (Central University)

Curated by ChEMBL
LigandPNGBDBM8960((+/-)-2-[(1-benzylpiperidin-4-yl)methyl]-5,6-dimet...)
Affinity DataIC50:  49nMAssay Description:Inhibition of electric eel AChE using acetylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition measured after 5 m...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Electrophorus electricus (Electric eel))
Jamia Millia Islamia (Central University)

Curated by ChEMBL
LigandPNGBDBM50524459(CHEMBL4437109)
Affinity DataIC50:  113nMAssay Description:Inhibition of electric eel AChE using acetylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition measured after 5 m...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCytochrome P450 2D6(Homo sapiens (Human))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50269061((1R)-6-Bromo-N-[(1R)-1-phenylethyl]-2,3,4,9-tetrah...)
Affinity DataIC50:  160nMAssay Description:Inhibition of CYP2D6More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50269061((1R)-6-Bromo-N-[(1R)-1-phenylethyl]-2,3,4,9-tetrah...)
Affinity DataIC50:  1.70E+3nMAssay Description:Inhibition of human ERGMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholinesterase(Equus caballus (Horse))
Jamia Millia Islamia (Central University)

Curated by ChEMBL
LigandPNGBDBM8960((+/-)-2-[(1-benzylpiperidin-4-yl)methyl]-5,6-dimet...)
Affinity DataIC50:  8.71E+3nMAssay Description:Inhibition of equine serum BuChE using butyrylthiocholine iodide as substrate pretreated for 5 mins followed by substrate addition measured after 5 m...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAmyloid-beta precursor protein(Homo sapiens (Human))
Jamia Millia Islamia (Central University)

Curated by ChEMBL
LigandPNGBDBM50524457(CHEMBL4453548)
Affinity DataIC50:  1.57E+4nMAssay Description:Inhibition of self-mediated amyloid beta (1 to 42) (unknown origin) aggregation incubated for 48 hrs by thioflavin-T fluorescence assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetAmyloid-beta precursor protein(Homo sapiens (Human))
Jamia Millia Islamia (Central University)

Curated by ChEMBL
LigandPNGBDBM50524456(CHEMBL4444093)
Affinity DataIC50:  1.79E+4nMAssay Description:Inhibition of self-mediated amyloid beta (1 to 42) (unknown origin) aggregation incubated for 48 hrs by thioflavin-T fluorescence assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50295257((R)-N-(6-chloro-2,3,4,9-tetrahydro-1H-carbazol-1-y...)
Affinity DataIC50: >2.00E+4nMAssay Description:Inhibition of human ERGMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50295256((R)-N-(6-chloro-2,3,4,9-tetrahydro-1H-carbazol-1-y...)
Affinity DataIC50: >2.00E+4nMAssay Description:Inhibition of human ERGMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytochrome P450 2D6(Homo sapiens (Human))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50295256((R)-N-(6-chloro-2,3,4,9-tetrahydro-1H-carbazol-1-y...)
Affinity DataIC50: >2.00E+4nMAssay Description:Inhibition of CYP2D6More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytochrome P450 2D6(Homo sapiens (Human))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50295257((R)-N-(6-chloro-2,3,4,9-tetrahydro-1H-carbazol-1-y...)
Affinity DataIC50: >2.00E+4nMAssay Description:Inhibition of CYP2D6More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50295255(6-bromo-N-phenyl-2,3,4,9-tetrahydro-1H-carbazol-1-...)
Affinity DataIC50: >3.00E+4nMAssay Description:Inhibition of human ERGMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytochrome P450 2D6(Homo sapiens (Human))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50295255(6-bromo-N-phenyl-2,3,4,9-tetrahydro-1H-carbazol-1-...)
Affinity DataIC50:  3.20E+4nMAssay Description:Inhibition of CYP2D6More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholinesterase(Equus caballus (Horse))
Jamia Millia Islamia (Central University)

Curated by ChEMBL
LigandPNGBDBM50524453(CHEMBL4569884)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of equine serum BuChE using butyrylthiocholine iodide as substrate pretreated for 5 mins followed by substrate addition measured after 5 m...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Electrophorus electricus (Electric eel))
Jamia Millia Islamia (Central University)

Curated by ChEMBL
LigandPNGBDBM50524458(CHEMBL4439198)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of electric eel AChE using acetylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition measured after 5 m...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCholinesterase(Equus caballus (Horse))
Jamia Millia Islamia (Central University)

Curated by ChEMBL
LigandPNGBDBM50524455(CHEMBL4560049)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of equine serum BuChE using butyrylthiocholine iodide as substrate pretreated for 5 mins followed by substrate addition measured after 5 m...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCholinesterase(Equus caballus (Horse))
Jamia Millia Islamia (Central University)

Curated by ChEMBL
LigandPNGBDBM50524456(CHEMBL4444093)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of equine serum BuChE using butyrylthiocholine iodide as substrate pretreated for 5 mins followed by substrate addition measured after 5 m...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCholinesterase(Equus caballus (Horse))
Jamia Millia Islamia (Central University)

Curated by ChEMBL
LigandPNGBDBM50524459(CHEMBL4437109)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of equine serum BuChE using butyrylthiocholine iodide as substrate pretreated for 5 mins followed by substrate addition measured after 5 m...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCholinesterase(Equus caballus (Horse))
Jamia Millia Islamia (Central University)

Curated by ChEMBL
LigandPNGBDBM50524458(CHEMBL4439198)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of equine serum BuChE using butyrylthiocholine iodide as substrate pretreated for 5 mins followed by substrate addition measured after 5 m...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Electrophorus electricus (Electric eel))
Jamia Millia Islamia (Central University)

Curated by ChEMBL
LigandPNGBDBM50524453(CHEMBL4569884)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of electric eel AChE using acetylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition measured after 5 m...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Electrophorus electricus (Electric eel))
Jamia Millia Islamia (Central University)

Curated by ChEMBL
LigandPNGBDBM50524457(CHEMBL4453548)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of electric eel AChE using acetylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition measured after 5 m...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCholinesterase(Equus caballus (Horse))
Jamia Millia Islamia (Central University)

Curated by ChEMBL
LigandPNGBDBM50524452(CHEMBL4451095)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of equine serum BuChE using butyrylthiocholine iodide as substrate pretreated for 5 mins followed by substrate addition measured after 5 m...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCholinesterase(Equus caballus (Horse))
Jamia Millia Islamia (Central University)

Curated by ChEMBL
LigandPNGBDBM50524454(CHEMBL4474224)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of equine serum BuChE using butyrylthiocholine iodide as substrate pretreated for 5 mins followed by substrate addition measured after 5 m...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCholinesterase(Equus caballus (Horse))
Jamia Millia Islamia (Central University)

Curated by ChEMBL
LigandPNGBDBM50524457(CHEMBL4453548)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of equine serum BuChE using butyrylthiocholine iodide as substrate pretreated for 5 mins followed by substrate addition measured after 5 m...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCholinesterase(Equus caballus (Horse))
Jamia Millia Islamia (Central University)

Curated by ChEMBL
LigandPNGBDBM50524460(CHEMBL4437847)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of equine serum BuChE using butyrylthiocholine iodide as substrate pretreated for 5 mins followed by substrate addition measured after 5 m...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetGenome polyprotein(Murine norovirus 1)
Chimerix

US Patent
LigandPNGBDBM263072(US9708359, 1 | US9708359, 122 | US9708359, 38 | US...)
Affinity DataEC50:  2.65E+3nMAssay Description:Polymerase reactions (10 μL) were conducted for 60 minutes at 37° C. Nucleoside triphosphates (NTPs) were present at 100 μM each, with 0.05...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetGenome polyprotein(Murine norovirus 1)
Chimerix

US Patent
LigandPNGBDBM263073(US9708359, 2)
Affinity DataEC50:  3.03E+3nMAssay Description:Polymerase reactions (10 μL) were conducted for 60 minutes at 37° C. Nucleoside triphosphates (NTPs) were present at 100 μM each, with 0.05...More data for this Ligand-Target Pair
Ligand InfoKEGGPC cidPC sid
In DepthDetails US Patent
TargetGenome polyprotein(Murine norovirus 1)
Chimerix

US Patent
LigandPNGBDBM263074(US9708359, 3)
Affinity DataEC50:  2.00E+3nMAssay Description:Polymerase reactions (10 μL) were conducted for 60 minutes at 37° C. Nucleoside triphosphates (NTPs) were present at 100 μM each, with 0.05...More data for this Ligand-Target Pair
Ligand InfoKEGGPC cidPC sid
In DepthDetails US Patent
TargetGenome polyprotein(Murine norovirus 1)
Chimerix

US Patent
LigandPNGBDBM263075(US9708359, 4)
Affinity DataEC50:  3.50E+3nMAssay Description:Polymerase reactions (10 μL) were conducted for 60 minutes at 37° C. Nucleoside triphosphates (NTPs) were present at 100 μM each, with 0.05...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetGenome polyprotein(Murine norovirus 1)
Chimerix

US Patent
LigandPNGBDBM263076(US9708359, 5)
Affinity DataEC50:  2.20E+3nMAssay Description:Polymerase reactions (10 μL) were conducted for 60 minutes at 37° C. Nucleoside triphosphates (NTPs) were present at 100 μM each, with 0.05...More data for this Ligand-Target Pair
Ligand InfoKEGGPC cidPC sid
In DepthDetails US Patent
TargetGenome polyprotein(Murine norovirus 1)
Chimerix

US Patent
LigandPNGBDBM263072(US9708359, 1 | US9708359, 122 | US9708359, 38 | US...)
Affinity DataEC50:  3.08E+3nMAssay Description:Polymerase reactions (10 μL) were conducted for 60 minutes at 37° C. Nucleoside triphosphates (NTPs) were present at 100 μM each, with 0.05...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetGenome polyprotein(Murine norovirus 1)
Chimerix

US Patent
LigandPNGBDBM263078(US9708359, 71)
Affinity DataEC50:  3.15E+3nMAssay Description:Polymerase reactions (10 μL) were conducted for 60 minutes at 37° C. Nucleoside triphosphates (NTPs) were present at 100 μM each, with 0.05...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetGenome polyprotein(Murine norovirus 1)
Chimerix

US Patent
LigandPNGBDBM263079(US9708359, 77)
Affinity DataEC50:  4.40E+3nMAssay Description:Polymerase reactions (10 μL) were conducted for 60 minutes at 37° C. Nucleoside triphosphates (NTPs) were present at 100 μM each, with 0.05...More data for this Ligand-Target Pair
Ligand InfoKEGGPC cidPC sid
In DepthDetails US Patent
TargetGenome polyprotein(Murine norovirus 1)
Chimerix

US Patent
LigandPNGBDBM263080(US9708359, 76)
Affinity DataEC50:  1.64E+4nMAssay Description:Polymerase reactions (10 μL) were conducted for 60 minutes at 37° C. Nucleoside triphosphates (NTPs) were present at 100 μM each, with 0.05...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetGenome polyprotein(Murine norovirus 1)
Chimerix

US Patent
LigandPNGBDBM263081(US9708359, 107)
Affinity DataEC50:  1.81E+4nMAssay Description:Polymerase reactions (10 μL) were conducted for 60 minutes at 37° C. Nucleoside triphosphates (NTPs) were present at 100 μM each, with 0.05...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetGenome polyprotein(Murine norovirus 1)
Chimerix

US Patent
LigandPNGBDBM263082(US9708359, 111)
Affinity DataEC50:  2.10E+4nMAssay Description:Polymerase reactions (10 μL) were conducted for 60 minutes at 37° C. Nucleoside triphosphates (NTPs) were present at 100 μM each, with 0.05...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetGenome polyprotein(Murine norovirus 1)
Chimerix

US Patent
LigandPNGBDBM263083(US9708359, 126)
Affinity DataEC50:  3.36E+4nMAssay Description:Polymerase reactions (10 μL) were conducted for 60 minutes at 37° C. Nucleoside triphosphates (NTPs) were present at 100 μM each, with 0.05...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
Displayed 1 to 50 (of 181 total ) | Next | Last >>
Jump to: