Compile Data Set for Download or QSAR
maximum 50k data
Found 16 Enz. Inhib. hit(s) with all data for entry = 50004887
TargetRenin(Homo sapiens (Human))
Bristol-Myers Squibb Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50029588((2R,3S)-3-[(S)-2-((S)-2-tert-Butoxycarbonylamino-3...)
Affinity DataIC50:  5nMAssay Description:Evaluation of inhibitory activity of the compound against human reninMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetRenin(Homo sapiens (Human))
Bristol-Myers Squibb Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50029584(CHEMBL334907 | [(1S,2S)-3-Cyclohexyl-1-hydroxy-2-(...)
Affinity DataIC50:  8.5nMAssay Description:Evaluation of inhibitory activity of the compound against human reninMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetRenin(Homo sapiens (Human))
Bristol-Myers Squibb Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50029580(CHEMBL344155 | {(1S,2S)-2-[(S)-2-((S)-2-tert-Butox...)
Affinity DataIC50:  10nMAssay Description:Evaluation of inhibitory activity of the compound against human renin.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetRenin(Homo sapiens (Human))
Bristol-Myers Squibb Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50029589(3-[(S)-2-((S)-2-tert-Butoxycarbonylamino-3-phenyl-...)
Affinity DataIC50:  15nMAssay Description:Evaluation of inhibitory activity of the compound against human reninMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetRenin(Homo sapiens (Human))
Bristol-Myers Squibb Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50029591(((1S,2S)-3-Cyclohexyl-2-{(S)-2-[(S)-2-(cyclopentan...)
Affinity DataIC50:  16nMAssay Description:Evaluation of inhibitory activity of the compound against human reninMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetRenin(Homo sapiens (Human))
Bristol-Myers Squibb Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50029586(CHEMBL407513 | {(1S,2S)-2-[(S)-2-((S)-2-tert-Butox...)
Affinity DataIC50:  29nMAssay Description:Evaluation of inhibitory activity of the compound against human renin.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetRenin(Homo sapiens (Human))
Bristol-Myers Squibb Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50029592(((1S,2S)-2-{(S)-2-[(S)-2-(6-Amino-hexanoylamino)-3...)
Affinity DataIC50:  31nMAssay Description:Evaluation of inhibitory activity of the compound against human reninMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetRenin(Homo sapiens (Human))
Bristol-Myers Squibb Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50029578(((1S,2S)-3-Cyclohexyl-2-{(S)-2-[(S)-2-(cyclopentan...)
Affinity DataIC50:  38nMAssay Description:Evaluation of inhibitory activity of the compound against human renin.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetRenin(Homo sapiens (Human))
Bristol-Myers Squibb Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50029582(CHEMBL336245 | [(1S,2S)-3-Cyclohexyl-1-hydroxy-2-(...)
Affinity DataIC50:  41nMAssay Description:Evaluation of inhibitory activity of the compound against human reninMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetRenin(Homo sapiens (Human))
Bristol-Myers Squibb Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50029581(((S)-3-Cyclohexyl-2-{(S)-2-[(S)-2-(cyclopentanecar...)
Affinity DataIC50:  44nMAssay Description:Evaluation of inhibitory activity of the compound against human renin. value in parentheses indicate no. of determinationsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetRenin(Homo sapiens (Human))
Bristol-Myers Squibb Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50029581(((S)-3-Cyclohexyl-2-{(S)-2-[(S)-2-(cyclopentanecar...)
Affinity DataIC50:  44nMAssay Description:Evaluation of inhibitory activity of the compound against human renin. value in parentheses indicate no. of determinationsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetRenin(Homo sapiens (Human))
Bristol-Myers Squibb Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50029579(CHEMBL436018 | {(1S,2S)-3-Cyclohexyl-2-[(S)-2-[(S)...)
Affinity DataIC50:  220nMAssay Description:Evaluation of inhibitory activity of the compound against human reninMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetRenin(Homo sapiens (Human))
Bristol-Myers Squibb Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50029590(CHEMBL140422 | Cyclopentanecarboxylic acid ((S)-1-...)
Affinity DataIC50:  400nMAssay Description:Evaluation of inhibitory activity of the compound against human renin. value in parentheses indicate no. of determinationsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetRenin(Homo sapiens (Human))
Bristol-Myers Squibb Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50029583(CHEMBL343814 | Cyclopentanecarboxylic acid ((S)-1-...)
Affinity DataIC50:  5.20E+3nMAssay Description:Evaluation of inhibitory activity of the compound against human renin. value in parentheses indicate no. of determinationsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetRenin(Homo sapiens (Human))
Bristol-Myers Squibb Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50029587(((1S,2S)-3-Cyclohexyl-2-{(S)-2-[(S)-2-(cyclopentan...)
Affinity DataIC50:  2.70E+4nMAssay Description:Evaluation of inhibitory activity of the compound against human reninMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetRenin(Homo sapiens (Human))
Bristol-Myers Squibb Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50029585(CHEMBL140146 | {(1R,2S)-2-[(S)-2-((S)-2-tert-Butox...)
Affinity DataIC50:  4.10E+4nMAssay Description:Evaluation of inhibitory activity of the compound against human renin.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed