Compile Data Set for Download or QSAR
Found 74 with Last Name = 'davies' and Initial = 'jw'
TargetB2 bradykinin receptor(RAT)
Novartis Institute for Medical Sciences

Curated by ChEMBL
LigandPNGBDBM50370083(CHEMBL1907651)copy SMILEScopy InChI
Affinity DataKi:  0.0230nMAssay Description:Inhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranesMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2X067SGPubMed
TargetB2 bradykinin receptor(RAT)
Novartis Institute for Medical Sciences

Curated by ChEMBL
LigandPNGBDBM50370077(CHEMBL1907652)copy SMILEScopy InChI
Affinity DataKi:  0.310nMAssay Description:Inhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranesMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2X067SGPubMed
TargetB2 bradykinin receptor(RAT)
Novartis Institute for Medical Sciences

Curated by ChEMBL
LigandPNGBDBM50113263((S)-1-[4-(4-benzhydrylthiosemicarbazido)-3-nitrobe...)copy SMILEScopy InChI
Affinity DataKi:  0.5nMAssay Description:Inhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranesMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2X067SGPubMed
TargetB2 bradykinin receptor(RAT)
Novartis Institute for Medical Sciences

Curated by ChEMBL
LigandPNGBDBM50113263((S)-1-[4-(4-benzhydrylthiosemicarbazido)-3-nitrobe...)copy SMILEScopy InChI
Affinity DataKi:  0.600nMAssay Description:Inhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranesMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2X067SGPubMed
TargetB2 bradykinin receptor(Homo sapiens (Human))
Novartis Institute for Medical Sciences

Curated by ChEMBL
LigandPNGBDBM50409527(CHEMBL2112283)copy SMILEScopy InChI
Affinity DataKi:  0.790nMAssay Description:Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2X067SGPubMed
TargetB2 bradykinin receptor(Homo sapiens (Human))
Novartis Institute for Medical Sciences

Curated by ChEMBL
LigandPNGBDBM50409529(CHEMBL2112221)copy SMILEScopy InChI
Affinity DataKi:  1.47nMAssay Description:Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2X067SGPubMed
TargetB2 bradykinin receptor(Homo sapiens (Human))
Novartis Institute for Medical Sciences

Curated by ChEMBL
LigandPNGBDBM50409528(CHEMBL2112220)copy SMILEScopy InChI
Affinity DataKi:  2.79nMAssay Description:Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2X067SGPubMed
TargetB2 bradykinin receptor(Homo sapiens (Human))
Novartis Institute for Medical Sciences

Curated by ChEMBL
LigandPNGBDBM50370080(CHEMBL1907656)copy SMILEScopy InChI
Affinity DataKi:  4.67nMAssay Description:Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2X067SGPubMed
TargetB2 bradykinin receptor(RAT)
Novartis Institute for Medical Sciences

Curated by ChEMBL
LigandPNGBDBM50370081(CHEMBL1907654)copy SMILEScopy InChI
Affinity DataKi:  5.46nMAssay Description:Inhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranesMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2X067SGPubMed
TargetB2 bradykinin receptor(RAT)
Novartis Institute for Medical Sciences

Curated by ChEMBL
LigandPNGBDBM50370078(CHEMBL1907653)copy SMILEScopy InChI
Affinity DataKi:  7.30nMAssay Description:Inhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranesMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2X067SGPubMed
TargetB2 bradykinin receptor(RAT)
Novartis Institute for Medical Sciences

Curated by ChEMBL
LigandPNGBDBM50409527(CHEMBL2112283)copy SMILEScopy InChI
Affinity DataKi:  10.7nMAssay Description:Inhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranesMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2X067SGPubMed
TargetB2 bradykinin receptor(RAT)
Novartis Institute for Medical Sciences

Curated by ChEMBL
LigandPNGBDBM50370080(CHEMBL1907656)copy SMILEScopy InChI
Affinity DataKi:  14.5nMAssay Description:Inhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranesMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2X067SGPubMed
TargetB2 bradykinin receptor(Homo sapiens (Human))
Novartis Institute for Medical Sciences

Curated by ChEMBL
LigandPNGBDBM50370081(CHEMBL1907654)copy SMILEScopy InChI
Affinity DataKi:  34.1nMAssay Description:Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2X067SGPubMed
TargetB2 bradykinin receptor(RAT)
Novartis Institute for Medical Sciences

Curated by ChEMBL
LigandPNGBDBM50409529(CHEMBL2112221)copy SMILEScopy InChI
Affinity DataKi:  64.5nMAssay Description:Inhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranesMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2X067SGPubMed
TargetB2 bradykinin receptor(Homo sapiens (Human))
Novartis Institute for Medical Sciences

Curated by ChEMBL
LigandPNGBDBM50370077(CHEMBL1907652)copy SMILEScopy InChI
Affinity DataKi:  95nMAssay Description:Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2X067SGPubMed
TargetB2 bradykinin receptor(Homo sapiens (Human))
Novartis Institute for Medical Sciences

Curated by ChEMBL
LigandPNGBDBM50370083(CHEMBL1907651)copy SMILEScopy InChI
Affinity DataKi:  119nMAssay Description:Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2X067SGPubMed
TargetB2 bradykinin receptor(RAT)
Novartis Institute for Medical Sciences

Curated by ChEMBL
LigandPNGBDBM50409528(CHEMBL2112220)copy SMILEScopy InChI
Affinity DataKi:  176nMAssay Description:Inhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranesMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2X067SGPubMed
TargetB2 bradykinin receptor(Homo sapiens (Human))
Novartis Institute for Medical Sciences

Curated by ChEMBL
LigandPNGBDBM50113264(1-[4-(4-benzhydrylthiosemicarbazido)-3-nitrobenzen...)copy SMILEScopy InChI
Affinity DataKi:  237nMAssay Description:Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2X067SGPubMed
TargetB2 bradykinin receptor(Homo sapiens (Human))
Novartis Institute for Medical Sciences

Curated by ChEMBL
LigandPNGBDBM50409530(CHEMBL2112219)copy SMILEScopy InChI
Affinity DataKi:  253nMAssay Description:Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2X067SGPubMed
TargetB2 bradykinin receptor(Homo sapiens (Human))
Novartis Institute for Medical Sciences

Curated by ChEMBL
LigandPNGBDBM50370082(CHEMBL1907655)copy SMILEScopy InChI
Affinity DataKi:  299nMAssay Description:Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2X067SGPubMed
TargetB2 bradykinin receptor(Homo sapiens (Human))
Novartis Institute for Medical Sciences

Curated by ChEMBL
LigandPNGBDBM50370084(CHEMBL1907657)copy SMILEScopy InChI
Affinity DataKi:  645nMAssay Description:Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2X067SGPubMed
TargetB2 bradykinin receptor(RAT)
Novartis Institute for Medical Sciences

Curated by ChEMBL
LigandPNGBDBM50370082(CHEMBL1907655)copy SMILEScopy InChI
Affinity DataKi:  654nMAssay Description:Inhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranesMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2X067SGPubMed
TargetB2 bradykinin receptor(Homo sapiens (Human))
Novartis Institute for Medical Sciences

Curated by ChEMBL
LigandPNGBDBM50113263((S)-1-[4-(4-benzhydrylthiosemicarbazido)-3-nitrobe...)copy SMILEScopy InChI
Affinity DataKi:  772nMAssay Description:Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2X067SGPubMed
TargetB2 bradykinin receptor(Homo sapiens (Human))
Novartis Institute for Medical Sciences

Curated by ChEMBL
LigandPNGBDBM50113263((S)-1-[4-(4-benzhydrylthiosemicarbazido)-3-nitrobe...)copy SMILEScopy InChI
Affinity DataKi:  1.43E+3nMAssay Description:Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2X067SGPubMed
TargetEstrogen receptor beta(Homo sapiens (Human))
Novartis Institutes for BioMedical Research

Curated by ChEMBL
LigandPNGBDBM50154137(3-(6-HYDROXY-NAPHTHALEN-2-YL)-BENZO[D]ISOOXAZOL-6-...)copy SMILEScopy InChI
Affinity DataIC50: 1nMAssay Description:Inhibition of estrogen receptor betaMore data for this Ligand-Target Pair
TargetEstrogen receptor beta(Homo sapiens (Human))
Novartis Institutes for BioMedical Research

Curated by ChEMBL
LigandPNGBDBM50154078(7-Bromo-2-(4-hydroxy-2-methyl-phenyl)-benzooxazol-...)copy SMILEScopy InChI
Affinity DataIC50: 1nMAssay Description:Inhibition of estrogen receptor betaMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2GX4CF5PubMed
TargetB2 bradykinin receptor(RAT)
Novartis Institute for Medical Sciences

Curated by ChEMBL
LigandPNGBDBM50409528(CHEMBL2112220)copy SMILEScopy InChI
Affinity DataIC50: 1.90nMAssay Description:Inhibition of Bradykinin receptor B2-mediated contractions of rat uterus smooth muscleMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2X067SGPubMed
TargetB2 bradykinin receptor(RAT)
Novartis Institute for Medical Sciences

Curated by ChEMBL
LigandPNGBDBM50409527(CHEMBL2112283)copy SMILEScopy InChI
Affinity DataIC50: 2.40nMAssay Description:Inhibition of Bradykinin receptor B2-mediated contractions of rat uterus smooth muscleMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2X067SGPubMed
TargetEstrogen receptor beta(Homo sapiens (Human))
Novartis Institutes for BioMedical Research

Curated by ChEMBL
LigandPNGBDBM50154062(2-(5-HYDROXY-NAPHTHALEN-1-YL)-1,3-BENZOOXAZOL-6-OL...)copy SMILEScopy InChI
Affinity DataIC50: 5nMAssay Description:Inhibition of estrogen receptor betaMore data for this Ligand-Target Pair
TargetB2 bradykinin receptor(Homo sapiens (Human))
Novartis Institute for Medical Sciences

Curated by ChEMBL
LigandPNGBDBM50409528(CHEMBL2112220)copy SMILEScopy InChI
Affinity DataIC50: 12nMAssay Description:Antagonism of the [Ca2+] efflux actions of the human Bradykinin receptor B2 (SK-N-SH neuroblastoma)More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2X067SGPubMed
TargetB2 bradykinin receptor(Homo sapiens (Human))
Novartis Institute for Medical Sciences

Curated by ChEMBL
LigandPNGBDBM50409527(CHEMBL2112283)copy SMILEScopy InChI
Affinity DataIC50: 17nMAssay Description:Antagonism of the [Ca2+] efflux actions of human Bradykinin receptor B2 (WI38 fibroblasts)More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2X067SGPubMed
TargetNitric oxide synthase, inducible(Homo sapiens (Human))
Novartis Institutes for BioMedical Research

Curated by ChEMBL
LigandPNGBDBM50148169((4-Chloro-phenyl)-[4-(4-methoxy-pyridin-2-ylamino)...)copy SMILEScopy InChI
Affinity DataIC50: 53nMAssay Description:Inhibition of iNOSMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2GX4CF5PubMed
TargetB2 bradykinin receptor(Homo sapiens (Human))
Novartis Institute for Medical Sciences

Curated by ChEMBL
LigandPNGBDBM50409528(CHEMBL2112220)copy SMILEScopy InChI
Affinity DataIC50: 55nMAssay Description:Antagonism of the [Ca2+] efflux actions of the human Bradykinin receptor B2 (WI38 fibroblasts)More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2X067SGPubMed
TargetNitric oxide synthase, inducible(Homo sapiens (Human))
Novartis Institutes for BioMedical Research

Curated by ChEMBL
LigandPNGBDBM50124525(4'-amino-5'-fluorospiro[hexahydropyridine-4,2'-(1'...)copy SMILEScopy InChI
Affinity DataIC50: 67nMAssay Description:Inhibition of iNOSMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2GX4CF5PubMed
TargetAromatase(Homo sapiens (Human))
Novartis Institutes for BioMedical Research

Curated by ChEMBL
LigandPNGBDBM50035206(4-(5-Methoxy-1a,2,3,7b-tetrahydro-1H-cyclopropa[a]...)copy SMILEScopy InChI
Affinity DataIC50: 69nMAssay Description:Inhibition of aromataseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2GX4CF5PubMed
TargetEstrogen receptor beta(Homo sapiens (Human))
Novartis Institutes for BioMedical Research

Curated by ChEMBL
LigandPNGBDBM19956(3-arylquinazolinethione, 1bd | 7-hydroxy-3-(4-hydr...)copy SMILEScopy InChI
Affinity DataIC50: 79nMAssay Description:Inhibition of estrogen receptor betaMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2GX4CF5PubMed
TargetNitric oxide synthase, inducible(Homo sapiens (Human))
Novartis Institutes for BioMedical Research

Curated by ChEMBL
LigandPNGBDBM50148164(4-(4-Methoxy-pyridin-2-ylamino)-piperidine-1-carbo...)copy SMILEScopy InChI
Affinity DataIC50: 89nMAssay Description:Inhibition of iNOSMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2GX4CF5PubMed
TargetB2 bradykinin receptor(Homo sapiens (Human))
Novartis Institute for Medical Sciences

Curated by ChEMBL
LigandPNGBDBM50409527(CHEMBL2112283)copy SMILEScopy InChI
Affinity DataIC50: 91nMAssay Description:Antagonism of the [Ca2+] efflux actions of human Bradykinin receptor B2 (SK-N-SH neuroblastoma)More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2X067SGPubMed
TargetAromatase(Homo sapiens (Human))
Novartis Institutes for BioMedical Research

Curated by ChEMBL
LigandPNGBDBM10009(1-[(6-Methoxybenzofuran-2-yl)-p-tolylmethyl]-1H-1,...)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:Inhibition of aromataseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2GX4CF5PubMed
TargetB2 bradykinin receptor(RAT)
Novartis Institute for Medical Sciences

Curated by ChEMBL
LigandPNGBDBM50409527(CHEMBL2112283)copy SMILEScopy InChI
Affinity DataIC50: 105nMAssay Description:Inhibition of increase in [Ca2+] efflux from NG108-15 cells caused by activation of rat Bradykinin receptor B2More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2X067SGPubMed
TargetB2 bradykinin receptor(RAT)
Novartis Institute for Medical Sciences

Curated by ChEMBL
LigandPNGBDBM50409528(CHEMBL2112220)copy SMILEScopy InChI
Affinity DataIC50: 141nMAssay Description:Inhibition of increase in [Ca2+] efflux from NG108-15 cells caused by activation of rat Bradykinin receptor B2More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2X067SGPubMed
TargetAromatase(Homo sapiens (Human))
Novartis Institutes for BioMedical Research

Curated by ChEMBL
LigandPNGBDBM10002((6-Methoxybenzofuran-2-yl)-(4-methoxyphenyl)-3-pyr...)copy SMILEScopy InChI
Affinity DataIC50: 160nMAssay Description:Inhibition of aromataseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2GX4CF5PubMed
TargetAromatase(Homo sapiens (Human))
Novartis Institutes for BioMedical Research

Curated by ChEMBL
LigandPNGBDBM9471(4-(1H-Imidazol-1-ylmethyl)-7-methoxy-2H-chromen-2-...)copy SMILEScopy InChI
Affinity DataIC50: 280nMAssay Description:Inhibition of aromataseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2GX4CF5PubMed
TargetNitric oxide synthase, inducible(Homo sapiens (Human))
Novartis Institutes for BioMedical Research

Curated by ChEMBL
LigandPNGBDBM50124528(CHEMBL170176 | ethyl 4'-amino-1H,1'H-spiro[piperid...)copy SMILEScopy InChI
Affinity DataIC50: 300nMAssay Description:Inhibition of iNOSMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2GX4CF5PubMed
TargetNitric oxide synthase, inducible(Homo sapiens (Human))
Novartis Institutes for BioMedical Research

Curated by ChEMBL
LigandPNGBDBM50091813(4-Ethyl-pyridin-2-ylamine | 4-ethylpyridin-2-amine...)copy SMILEScopy InChI
Affinity DataIC50: 1.10E+3nMAssay Description:Inhibition of iNOSMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2GX4CF5PubMed
TargetEstrogen receptor beta(Homo sapiens (Human))
Novartis Institutes for BioMedical Research

Curated by ChEMBL
LigandPNGBDBM50376217(CHEMBL362476)copy SMILEScopy InChI
Affinity DataIC50: 1.10E+3nMAssay Description:Inhibition of estrogen receptor betaMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2GX4CF5PubMed
TargetNitric oxide synthase, inducible(Homo sapiens (Human))
Novartis Institutes for BioMedical Research

Curated by ChEMBL
LigandPNGBDBM50237936(4-Ethyl-5,6-dihydro-1H-pyridin-(2Z)-ylideneamine |...)copy SMILEScopy InChI
Affinity DataIC50: 1.20E+3nMAssay Description:Inhibition of iNOSMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2GX4CF5PubMed
TargetNitric oxide synthase, inducible(Homo sapiens (Human))
Novartis Institutes for BioMedical Research

Curated by ChEMBL
LigandPNGBDBM50376215(CHEMBL409050)copy SMILEScopy InChI
Affinity DataIC50: 1.20E+3nMAssay Description:Inhibition of iNOSMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2GX4CF5PubMed
TargetEstrogen receptor beta(Homo sapiens (Human))
Novartis Institutes for BioMedical Research

Curated by ChEMBL
LigandPNGBDBM50376221(CHEMBL261781)copy SMILEScopy InChI
Affinity DataIC50: 1.20E+3nMAssay Description:Inhibition of estrogen receptor betaMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2GX4CF5PubMed
TargetNitric oxide synthase, inducible(Homo sapiens (Human))
Novartis Institutes for BioMedical Research

Curated by ChEMBL
LigandPNGBDBM50117550((3aR,9bS)-7-methoxy-2,3,3a,9b-tetrahydro-1H-cyclop...)copy SMILEScopy InChI
Affinity DataIC50: 1.40E+3nMAssay Description:Inhibition of iNOSMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2GX4CF5PubMed
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