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

Curated by ChEMBL
LigandPNGBDBM50029588(3-[2-(2-tert-Butoxycarbonylamino-3-phenyl-propiony...)
Affinity DataIC50: 5nMAssay Description:Evaluation of inhibitory activity against human reninMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetRenin(Human)
Bristol-Myers Squibb Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50029584([(1S,2S)-3-Cyclohexyl-1-hydroxy-2-((S)-4-methyl-2-...)
Affinity DataIC50: 8.5nMAssay Description:Evaluation of inhibitory activity against human reninMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetRenin(Human)
Bristol-Myers Squibb Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50029580({(1S,2S)-2-[(S)-2-((S)-2-tert-Butoxycarbonylamino-...)
Affinity DataIC50: 10nMAssay Description:Evaluation of inhibitory activity against human renin.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetRenin(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 against human reninMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetRenin(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 against human reninMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetRenin(Human)
Bristol-Myers Squibb Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50029586({(1S,2S)-2-[(S)-2-((S)-2-tert-Butoxycarbonylamino-...)
Affinity DataIC50: 29nMAssay Description:Evaluation of inhibitory activity against human renin.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetRenin(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 against human reninMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetRenin(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 against human renin.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetRenin(Human)
Bristol-Myers Squibb Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50029582([(1S,2S)-3-Cyclohexyl-1-hydroxy-2-((S)-3-(1H-imida...)
Affinity DataIC50: 41nMAssay Description:Evaluation of inhibitory activity against human reninMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetRenin(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 against human renin. value in parentheses indicate no. of determinationsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetRenin(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 against human renin. value in parentheses indicate no. of determinationsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetRenin(Human)
Bristol-Myers Squibb Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50029579({(1S,2S)-3-Cyclohexyl-2-[(S)-2-[(S)-2-(cyclopentan...)
Affinity DataIC50: 220nMAssay Description:Evaluation of inhibitory activity against human reninMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetRenin(Human)
Bristol-Myers Squibb Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50029590(Cyclopentanecarboxylic acid ((S)-1-{(S)-1-[(1S,2S)...)
Affinity DataIC50: 400nMAssay Description:Evaluation of inhibitory activity against human renin. value in parentheses indicate no. of determinationsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetRenin(Human)
Bristol-Myers Squibb Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50029583(Cyclopentanecarboxylic acid ((S)-1-{(S)-1-[(1S,2R)...)
Affinity DataIC50: 5.20E+3nMAssay Description:Evaluation of inhibitory activity against human renin. value in parentheses indicate no. of determinationsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetRenin(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 against human reninMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetRenin(Human)
Bristol-Myers Squibb Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50029585({(1R,2S)-2-[(S)-2-((S)-2-tert-Butoxycarbonylamino-...)
Affinity DataIC50: 4.10E+4nMAssay Description:Evaluation of inhibitory activity against human renin.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed