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Found 6 Enz. Inhib. hit(s) with all data for entry = 50011005
TargetChymase(Homo sapiens (Human))
Shionogi

Curated by ChEMBL
LigandPNGBDBM50093745((6R,7R)-7-(2-Ethoxy-benzoylamino)-7-methoxy-3-(1-m...)
Affinity DataIC50:  27nMAssay Description:Compound was evaluated for its inhibitory activity against human Serine protease chymaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetChymase(Homo sapiens (Human))
Shionogi

Curated by ChEMBL
LigandPNGBDBM50101142(2-((E)-1-Methoxy-3-phenyl-allylidene)-cyclopent-4-...)
Affinity DataIC50:  1.70E+3nMAssay Description:Compound was evaluated for its inhibitory activity against human Serine protease chymaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetChymase(Homo sapiens (Human))
Shionogi

Curated by ChEMBL
LigandPNGBDBM50101141(2-((E)-3-Phenyl-allylidene)-cyclopent-4-ene-1,3-di...)
Affinity DataIC50:  1.20E+4nMAssay Description:Compound was evaluated for its inhibitory activity against human Serine protease chymaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetChymase(Homo sapiens (Human))
Shionogi

Curated by ChEMBL
LigandPNGBDBM50101140(4,5-Dimethoxy-2-((E)-1-methoxy-3-phenyl-allylidene...)
Affinity DataIC50:  3.00E+4nMAssay Description:Compound was evaluated for its inhibitory activity against human Serine protease chymaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetChymase(Homo sapiens (Human))
Shionogi

Curated by ChEMBL
LigandPNGBDBM50101139(2-(1-Methoxy-3-phenyl-propylidene)-cyclopent-4-ene...)
Affinity DataIC50:  4.00E+4nMAssay Description:Compound was evaluated for its inhibitory activity against human Serine protease chymaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetChymase(Homo sapiens (Human))
Shionogi

Curated by ChEMBL
LigandPNGBDBM50101138(2-(1-Methoxy-ethylidene)-cyclopent-4-ene-1,3-dione...)
Affinity DataIC50: >1.00E+6nMAssay Description:Compound was evaluated for its inhibitory activity against human chymaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed