Compile Data Set for Download or QSAR
Found 364 with Last Name = 'ohtsuka' and Initial = 't'
TargetChymase(Homo sapiens (Human))
Welfide Corporation

Curated by ChEMBL
LigandPNGBDBM50098853(2-(2-{2-[5-Amino-2-(3-methoxy-phenyl)-6-oxo-6H-pyr...)copy SMILEScopy InChI
Affinity DataKi:  1.12nMAssay Description:Inhibitory activity against canine skin chymaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q26H4J4KPubMed
TargetChymase(Homo sapiens (Human))
Welfide Corporation

Curated by ChEMBL
LigandPNGBDBM50098874(4-{2-[5-Amino-2-(3-chloro-phenyl)-6-oxo-6H-pyrimid...)copy SMILEScopy InChI
Affinity DataKi:  2.62nMAssay Description:In vitro inhibitory activity was determined against human heart chymaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22R3SCDPubMed
TargetChymase(Homo sapiens (Human))
Welfide Corporation

Curated by ChEMBL
LigandPNGBDBM50098868(4-[2-(5-Amino-6-oxo-2-m-tolyl-6H-pyrimidin-1-yl)-a...)copy SMILEScopy InChI
Affinity DataKi:  3.56nMAssay Description:In vitro inhibitory activity was determined against human heart chymaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22R3SCDPubMed
TargetChymase(Homo sapiens (Human))
Welfide Corporation

Curated by ChEMBL
LigandPNGBDBM50098847(2-(2-{2-[5-Amino-2-(4-fluoro-phenyl)-6-oxo-6H-pyri...)copy SMILEScopy InChI
Affinity DataKi:  3.68nMAssay Description:Inhibitory activity against canine skin chymaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q26H4J4KPubMed
TargetChymase(Homo sapiens (Human))
Welfide Corporation

Curated by ChEMBL
LigandPNGBDBM50098853(2-(2-{2-[5-Amino-2-(3-methoxy-phenyl)-6-oxo-6H-pyr...)copy SMILEScopy InChI
Affinity DataKi:  4.85nMAssay Description:Inhibitory activity evaluated against chymase from human heart.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q26H4J4KPubMed
TargetChymase(Homo sapiens (Human))
Welfide Corporation

Curated by ChEMBL
LigandPNGBDBM50098854(2-{2-[2-(5-Amino-6-oxo-2-phenyl-6H-pyrimidin-1-yl)...)copy SMILEScopy InChI
Affinity DataKi:  5.57nMAssay Description:Inhibitory activity evaluated against chymase from human heart.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q26H4J4KPubMed
TargetChymase(Homo sapiens (Human))
Welfide Corporation

Curated by ChEMBL
LigandPNGBDBM50068894(3-(4-{[(S)-1-((S)-2-tert-Butoxycarbonylamino-3-met...)copy SMILEScopy InChI
Affinity DataKi:  5.60nMAssay Description:In vitro inhibitory activity was determined against human heart chymaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22R3SCDPubMed
TargetChymase(Homo sapiens (Human))
Welfide Corporation

Curated by ChEMBL
LigandPNGBDBM50098841(2-(2-{2-[5-Amino-2-(3-amino-phenyl)-6-oxo-6H-pyrim...)copy SMILEScopy InChI
Affinity DataKi:  5.60nMAssay Description:Inhibitory activity evaluated against chymase from human heart.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q26H4J4KPubMed
TargetChymase(Homo sapiens (Human))
Welfide Corporation

Curated by ChEMBL
LigandPNGBDBM50098892(4-[2-(5-Amino-6-oxo-2-m-tolyl-6H-pyrimidin-1-yl)-a...)copy SMILEScopy InChI
Affinity DataKi:  7.71nMAssay Description:In vitro inhibitory activity was determined against human heart chymaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22R3SCDPubMed
TargetChymase(Homo sapiens (Human))
Welfide Corporation

Curated by ChEMBL
LigandPNGBDBM50098879(4-[2-(5-Amino-6-oxo-2-m-tolyl-6H-pyrimidin-1-yl)-a...)copy SMILEScopy InChI
Affinity DataKi:  9.32nMAssay Description:In vitro inhibitory activity was determined against human heart chymaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22R3SCDPubMed
TargetChymotrypsin-C(Homo sapiens (Human))
Welfide Corporation

Curated by ChEMBL
LigandPNGBDBM87059(CHEMBL247767 | Chymostatin)copy SMILEScopy InChI
Affinity DataKi:  9.36nMAssay Description:In vitro inhibitory activity was determined against bovine pancreas chymotrypsinMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22R3SCDPubMed
TargetChymotrypsin-C(Homo sapiens (Human))
Welfide Corporation

Curated by ChEMBL
LigandPNGBDBM87059(CHEMBL247767 | Chymostatin)copy SMILEScopy InChI
Affinity DataKi:  9.36nMAssay Description:inhibitory activity against alpha chymotrypsin from bovine pancreas.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q26H4J4KPubMed
TargetChymase(Homo sapiens (Human))
Welfide Corporation

Curated by ChEMBL
LigandPNGBDBM50098880(3-{4-[2-(5-Amino-6-oxo-2-m-tolyl-6H-pyrimidin-1-yl...)copy SMILEScopy InChI
Affinity DataKi:  9.70nMAssay Description:In vitro inhibitory activity was determined against human heart chymaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22R3SCDPubMed
TargetChymase(Homo sapiens (Human))
Welfide Corporation

Curated by ChEMBL
LigandPNGBDBM50098878(4-[2-(5-Amino-6-oxo-2-m-tolyl-6H-pyrimidin-1-yl)-a...)copy SMILEScopy InChI
Affinity DataKi:  10.2nMAssay Description:In vitro inhibitory activity was determined against human heart chymaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22R3SCDPubMed
TargetChymase(Homo sapiens (Human))
Welfide Corporation

Curated by ChEMBL
LigandPNGBDBM50098870(CHEMBL26182 | {4-[2-(5-Amino-6-oxo-2-m-tolyl-6H-py...)copy SMILEScopy InChI
Affinity DataKi:  10.2nMAssay Description:In vitro inhibitory activity was determined against human heart chymaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22R3SCDPubMed
TargetChymase(Homo sapiens (Human))
Welfide Corporation

Curated by ChEMBL
LigandPNGBDBM50098875(4-[2-(5-Amino-6-oxo-2-m-tolyl-6H-pyrimidin-1-yl)-a...)copy SMILEScopy InChI
Affinity DataKi:  12nMAssay Description:In vitro inhibitory activity was determined against human heart chymaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22R3SCDPubMed
TargetChymotrypsin-C(Homo sapiens (Human))
Welfide Corporation

Curated by ChEMBL
LigandPNGBDBM50098882(4-[2-(5-Amino-6-oxo-2-m-tolyl-6H-pyrimidin-1-yl)-a...)copy SMILEScopy InChI
Affinity DataKi:  12.6nMAssay Description:In vitro inhibitory activity was determined against bovine pancreas chymotrypsinMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22R3SCDPubMed
TargetChymase(Homo sapiens (Human))
Welfide Corporation

Curated by ChEMBL
LigandPNGBDBM87059(CHEMBL247767 | Chymostatin)copy SMILEScopy InChI
Affinity DataKi:  13.1nMAssay Description:In vitro inhibitory activity was determined against human heart chymaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22R3SCDPubMed
TargetChymase(Homo sapiens (Human))
Welfide Corporation

Curated by ChEMBL
LigandPNGBDBM87059(CHEMBL247767 | Chymostatin)copy SMILEScopy InChI
Affinity DataKi:  13.1nMAssay Description:inhibitory activity was evaluated against chymase from human heart.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q26H4J4KPubMed
TargetChymase(Homo sapiens (Human))
Welfide Corporation

Curated by ChEMBL
LigandPNGBDBM50098882(4-[2-(5-Amino-6-oxo-2-m-tolyl-6H-pyrimidin-1-yl)-a...)copy SMILEScopy InChI
Affinity DataKi:  13.3nMAssay Description:In vitro inhibitory activity was determined against human heart chymaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22R3SCDPubMed
TargetChymase(Homo sapiens (Human))
Welfide Corporation

Curated by ChEMBL
LigandPNGBDBM50098877(4-{2-[5-Amino-2-(3-methoxy-phenyl)-6-oxo-6H-pyrimi...)copy SMILEScopy InChI
Affinity DataKi:  13.8nMAssay Description:In vitro inhibitory activity was determined against human heart chymaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22R3SCDPubMed
TargetChymase(Homo sapiens (Human))
Welfide Corporation

Curated by ChEMBL
LigandPNGBDBM50098849(2-(2-{2-[5-Amino-2-(3-fluoro-phenyl)-6-oxo-6H-pyri...)copy SMILEScopy InChI
Affinity DataKi:  14.3nMAssay Description:Inhibitory activity evaluated against chymase from human heart.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q26H4J4KPubMed
TargetChymase(Homo sapiens (Human))
Welfide Corporation

Curated by ChEMBL
LigandPNGBDBM50098876(4-{2-[5-Amino-2-(3-fluoro-phenyl)-6-oxo-6H-pyrimid...)copy SMILEScopy InChI
Affinity DataKi:  15.7nMAssay Description:In vitro inhibitory activity was determined against human heart chymaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22R3SCDPubMed
TargetChymase(Homo sapiens (Human))
Welfide Corporation

Curated by ChEMBL
LigandPNGBDBM50098866(4-({4-[2-(5-Amino-6-oxo-2-m-tolyl-6H-pyrimidin-1-y...)copy SMILEScopy InChI
Affinity DataKi:  16.6nMAssay Description:In vitro inhibitory activity was determined against human heart chymaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22R3SCDPubMed
TargetChymase(Homo sapiens (Human))
Welfide Corporation

Curated by ChEMBL
LigandPNGBDBM50098891(4-[2-(5-Amino-6-oxo-2-m-tolyl-6H-pyrimidin-1-yl)-a...)copy SMILEScopy InChI
Affinity DataKi:  16.9nMAssay Description:In vitro inhibitory activity was determined against human heart chymaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22R3SCDPubMed
TargetChymase(Homo sapiens (Human))
Welfide Corporation

Curated by ChEMBL
LigandPNGBDBM50098872(CHEMBL442146 | {4-[2-(5-Amino-6-oxo-2-m-tolyl-6H-p...)copy SMILEScopy InChI
Affinity DataKi:  16.9nMAssay Description:In vitro inhibitory activity was determined against human heart chymaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22R3SCDPubMed
TargetChymase(Homo sapiens (Human))
Welfide Corporation

Curated by ChEMBL
LigandPNGBDBM50098889(4-[2-(5-Amino-6-oxo-2-m-tolyl-6H-pyrimidin-1-yl)-a...)copy SMILEScopy InChI
Affinity DataKi:  18.5nMAssay Description:In vitro inhibitory activity was determined against human heart chymaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22R3SCDPubMed
TargetGlycylpeptide N-tetradecanoyltransferase(Candida albicans (Yeast))
Nippon Roche Research Center

LigandPNGBDBM43856(4-ethoxy-N-[(6-fluoro-1,1-diketo-2,3-dihydrothioch...)copy SMILEScopy InChI
Affinity DataKi:  20nMAssay Description:Inhibition activity against C. albicans Nmt and human Nmt as assessed by IC50 using myristoyl-CoA (0.5 uM) and peptide substrate GLTISKLFRR-NH2 (0.5 ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BV7F0CPubMed
TargetChymase(Homo sapiens (Human))
Welfide Corporation

Curated by ChEMBL
LigandPNGBDBM50098847(2-(2-{2-[5-Amino-2-(4-fluoro-phenyl)-6-oxo-6H-pyri...)copy SMILEScopy InChI
Affinity DataKi:  22.6nMAssay Description:Inhibitory activity evaluated against chymase from human heart.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q26H4J4KPubMed
TargetChymase(Homo sapiens (Human))
Welfide Corporation

Curated by ChEMBL
LigandPNGBDBM50098867(3-{4-[2-(5-Amino-6-oxo-2-m-tolyl-6H-pyrimidin-1-yl...)copy SMILEScopy InChI
Affinity DataKi:  23nMAssay Description:In vitro inhibitory activity was determined against human heart chymaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22R3SCDPubMed
TargetChymotrypsinogen A(Bos taurus (bovine))
Welfide Corporation

Curated by ChEMBL
LigandPNGBDBM50098842(2-(2-{2-[5-Amino-2-(4-fluoro-phenyl)-6-oxo-6H-pyri...)copy SMILEScopy InChI
Affinity DataKi:  23.3nMAssay Description:Inhibitory activity against alpha chymotrypsin from bovine pancreas.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q26H4J4KPubMed
TargetChymase(Homo sapiens (Human))
Welfide Corporation

Curated by ChEMBL
LigandPNGBDBM50098844(2-(2-{2-[5-Amino-2-(3-chloro-phenyl)-6-oxo-6H-pyri...)copy SMILEScopy InChI
Affinity DataKi:  26.1nMAssay Description:Inhibitory activity evaluated against chymase from human heart.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q26H4J4KPubMed
TargetChymase(Homo sapiens (Human))
Welfide Corporation

Curated by ChEMBL
LigandPNGBDBM50098874(4-{2-[5-Amino-2-(3-chloro-phenyl)-6-oxo-6H-pyrimid...)copy SMILEScopy InChI
Affinity DataKi:  28nMAssay Description:Inhibitory activity against canine skin chymaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22R3SCDPubMed
TargetChymase(Homo sapiens (Human))
Welfide Corporation

Curated by ChEMBL
LigandPNGBDBM50098881(4-[2-(5-Amino-6-oxo-2-m-tolyl-6H-pyrimidin-1-yl)-a...)copy SMILEScopy InChI
Affinity DataKi:  28.9nMAssay Description:In vitro inhibitory activity was determined against human heart chymaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22R3SCDPubMed
TargetGlycylpeptide N-tetradecanoyltransferase(Candida albicans (Yeast))
Nippon Roche Research Center

LigandPNGBDBM43856(4-ethoxy-N-[(6-fluoro-1,1-diketo-2,3-dihydrothioch...)copy SMILEScopy InChI
Affinity DataKi:  30nM IC50: 30nMAssay Description:Inhibition activity against C. albicans Nmt and human Nmt as assessed by IC50 using myristoyl-CoA (0.5 uM) and peptide substrate GLTISKLFRR-NH2 (0.5 ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BV7F0CPubMed
TargetGlycylpeptide N-tetradecanoyltransferase(Candida albicans (Yeast))
Nippon Roche Research Center

LigandPNGBDBM43856(4-ethoxy-N-[(6-fluoro-1,1-diketo-2,3-dihydrothioch...)copy SMILEScopy InChI
Affinity DataKi:  30nMAssay Description:Inhibition activity against C. albicans Nmt and human Nmt as assessed by IC50 using myristoyl-CoA (0.5 uM) and peptide substrate GLTISKLFRR-NH2 (0.5 ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BV7F0CPubMed
TargetGlycylpeptide N-tetradecanoyltransferase(Candida albicans (Yeast))
Nippon Roche Research Center

LigandPNGBDBM43856(4-ethoxy-N-[(6-fluoro-1,1-diketo-2,3-dihydrothioch...)copy SMILEScopy InChI
Affinity DataKi:  30nMAssay Description:Inhibition activity against C. albicans Nmt and human Nmt as assessed by IC50 using myristoyl-CoA (0.5 uM) and peptide substrate GLTISKLFRR-NH2 (0.5 ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BV7F0CPubMed
TargetGlycylpeptide N-tetradecanoyltransferase(Candida albicans (Yeast))
Nippon Roche Research Center

LigandPNGBDBM43856(4-ethoxy-N-[(6-fluoro-1,1-diketo-2,3-dihydrothioch...)copy SMILEScopy InChI
Affinity DataKi:  30nMAssay Description:Inhibition activity against C. albicans Nmt and human Nmt as assessed by IC50 using myristoyl-CoA (0.5 uM) and peptide substrate GLTISKLFRR-NH2 (0.5 ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BV7F0CPubMed
TargetGlycylpeptide N-tetradecanoyltransferase(Candida albicans (Yeast))
Nippon Roche Research Center

LigandPNGBDBM43856(4-ethoxy-N-[(6-fluoro-1,1-diketo-2,3-dihydrothioch...)copy SMILEScopy InChI
Affinity DataKi:  30nMAssay Description:Inhibition activity against C. albicans Nmt and human Nmt as assessed by IC50 using myristoyl-CoA (0.5 uM) and peptide substrate GLTISKLFRR-NH2 (0.5 ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BV7F0CPubMed
TargetChymase(Homo sapiens (Human))
Welfide Corporation

Curated by ChEMBL
LigandPNGBDBM50098861(2-(2-{2-[5-Amino-2-(4-fluoro-phenyl)-6-oxo-6H-pyri...)copy SMILEScopy InChI
Affinity DataKi:  30nMAssay Description:Inhibitory activity evaluated against chymase from human heart.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q26H4J4KPubMed
TargetChymase(Homo sapiens (Human))
Welfide Corporation

Curated by ChEMBL
LigandPNGBDBM50098886(4-[2-(5-Amino-6-oxo-2-phenyl-6H-pyrimidin-1-yl)-ac...)copy SMILEScopy InChI
Affinity DataKi:  32.5nMAssay Description:In vitro inhibitory activity was determined against human heart chymaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22R3SCDPubMed
TargetChymotrypsinogen A(Bos taurus (bovine))
Welfide Corporation

Curated by ChEMBL
LigandPNGBDBM50098862(2-(2-{2-[5-Amino-2-(4-fluoro-phenyl)-6-oxo-6H-pyri...)copy SMILEScopy InChI
Affinity DataKi:  32.6nMAssay Description:Inhibitory activity against alpha chymotrypsin from bovine pancreas.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q26H4J4KPubMed
TargetChymase(Homo sapiens (Human))
Welfide Corporation

Curated by ChEMBL
LigandPNGBDBM50098883(4-[2-(5-Amino-6-oxo-2-m-tolyl-6H-pyrimidin-1-yl)-a...)copy SMILEScopy InChI
Affinity DataKi:  33.7nMAssay Description:In vitro inhibitory activity was determined against human heart chymaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q22R3SCDPubMed
TargetGlycylpeptide N-tetradecanoyltransferase(Candida albicans (Yeast))
Nippon Roche Research Center

LigandPNGBDBM43856(4-ethoxy-N-[(6-fluoro-1,1-diketo-2,3-dihydrothioch...)copy SMILEScopy InChI
Affinity DataKi:  40nMAssay Description:Inhibition activity against C. albicans Nmt and human Nmt as assessed by IC50 using myristoyl-CoA (0.5 uM) and peptide substrate GLTISKLFRR-NH2 (0.5 ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BV7F0CPubMed
TargetGlycylpeptide N-tetradecanoyltransferase(Candida albicans (Yeast))
Nippon Roche Research Center

LigandPNGBDBM43856(4-ethoxy-N-[(6-fluoro-1,1-diketo-2,3-dihydrothioch...)copy SMILEScopy InChI
Affinity DataKi:  40nMAssay Description:Inhibition activity against C. albicans Nmt and human Nmt as assessed by IC50 using myristoyl-CoA (0.5 uM) and peptide substrate GLTISKLFRR-NH2 (0.5 ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BV7F0CPubMed
TargetMast cell protease 9(Mus musculus)
Welfide Corporation

Curated by ChEMBL
LigandPNGBDBM50098847(2-(2-{2-[5-Amino-2-(4-fluoro-phenyl)-6-oxo-6H-pyri...)copy SMILEScopy InChI
Affinity DataKi:  40.4nMAssay Description:Inhibitory activity against mouse peritoneal chymaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q26H4J4KPubMed
TargetChymase(Homo sapiens (Human))
Welfide Corporation

Curated by ChEMBL
LigandPNGBDBM50098864(2-(2-{2-[5-Amino-2-(3-nitro-phenyl)-6-oxo-6H-pyrim...)copy SMILEScopy InChI
Affinity DataKi:  41.8nMAssay Description:Inhibitory activity evaluated against chymase from human heart.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q26H4J4KPubMed
TargetChymase(Homo sapiens (Human))
Welfide Corporation

Curated by ChEMBL
LigandPNGBDBM50098843(2-{2-[2-(5-Amino-6-oxo-2-pyridin-4-yl-6H-pyrimidin...)copy SMILEScopy InChI
Affinity DataKi:  43.5nMAssay Description:Inhibitory activity evaluated against chymase from human heart.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q26H4J4KPubMed
TargetChymase(Homo sapiens (Human))
Welfide Corporation

Curated by ChEMBL
LigandPNGBDBM50098838(2-{2-[2-(5-Amino-6-oxo-2-m-tolyl-6H-pyrimidin-1-yl...)copy SMILEScopy InChI
Affinity DataKi:  44.2nMAssay Description:Inhibitory activity evaluated against chymase from human heart.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q26H4J4KPubMed
TargetChymotrypsinogen A(Bos taurus (bovine))
Welfide Corporation

Curated by ChEMBL
LigandPNGBDBM50098839(2-{2-[2-(5-Amino-6-oxo-2-pyridin-3-yl-6H-pyrimidin...)copy SMILEScopy InChI
Affinity DataKi:  45.1nMAssay Description:Inhibitory activity against alpha chymotrypsin from bovine pancreas.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q26H4J4KPubMed
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