Compile Data Set for Download or QSAR
Report error Found 375 of affinity data for UniProtKB/TrEMBL: P47820
TargetAngiotensin-converting enzyme(Rat)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50050127BDBM50050127((S)-3-(4-Hydroxy-phenyl)-2-[(2S,3R)-2-((S)-2-merca...)
Affinity DataIC50: 0.260nMAssay Description:Inhibitory activity against angiotensin I converting enzymeMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/3/2012
Entry Details Article
PubMed
TargetAngiotensin-converting enzyme(Rat)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50050151BDBM50050151(1-[(S)-2-((S)-2-Mercapto-3-phenyl-propionylamino)-...)
Affinity DataIC50: 0.300nMAssay Description:Inhibitory activity against angiotensin I converting enzymeMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/3/2012
Entry Details Article
PubMed
TargetAngiotensin-converting enzyme(Rat)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50050149BDBM50050149(1-[(S)-2-((S)-2-Mercapto-4-phenyl-butyrylamino)-pr...)
Affinity DataIC50: 0.350nMAssay Description:Inhibitory activity against angiotensin I converting enzymeMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/3/2012
Entry Details Article
PubMed
TargetAngiotensin-converting enzyme(Rat)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50050150BDBM50050150(1-[(S)-2-((S)-2-Mercapto-3-phenyl-propionylamino)-...)
Affinity DataIC50: 0.400nMAssay Description:Inhibitory activity against angiotensin I converting enzymeMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/3/2012
Entry Details Article
PubMed
TargetAngiotensin-converting enzyme(Rat)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50051796BDBM50051796((2S,5R)-5-(2-Hydroxy-phenyl)-1-{2-[(S)-2-mercapto-...)
Affinity DataIC50: 0.420nMAssay Description:In vitro inhibition of rat angiotensin I converting enzymeMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/1/2012
Entry Details Article
PubMed
TargetAngiotensin-converting enzyme(Rat)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50051798BDBM50051798((2S,5R)-5-(4-Hydroxy-phenyl)-1-{2-[(S)-3-(4-hydrox...)
Affinity DataIC50: 0.460nMAssay Description:In vitro inhibition of rat angiotensin I converting enzymeMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/1/2012
Entry Details Article
PubMed
TargetAngiotensin-converting enzyme(Rat)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50051784BDBM50051784((2S,5R)-5-(2-Hydroxy-phenyl)-1-[2-((S)-2-mercapto-...)
Affinity DataIC50: 0.5nMAssay Description:In vitro inhibition of rat angiotensin I converting enzymeMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/1/2012
Entry Details Article
PubMed
TargetAngiotensin-converting enzyme(Rat)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50011193BDBM50011193(CHEMBL342372 | Utibaprilat | 5-tert-Butyl-3-[2-(1-...)
Affinity DataIC50: 0.510nMAssay Description:Compound was tested for inhibitory activity against angiotensin I converting enzymeMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAngiotensin-converting enzyme(Rat)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50051785BDBM50051785((2S,5R)-1-[2-((S)-2-Mercapto-3-phenyl-propionylami...)
Affinity DataIC50: 0.550nMAssay Description:In vitro inhibition of rat angiotensin I converting enzymeMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/1/2012
Entry Details Article
PubMed
TargetAngiotensin-converting enzyme(Rat)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50050156BDBM50050156((S)-1-[(S)-2-((2S,3S)-2-Mercapto-3-methyl-pentanoy...)
Affinity DataIC50: 0.580nMAssay Description:Inhibitory activity against angiotensin I converting enzymeMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/3/2012
Entry Details Article
PubMed
TargetAngiotensin-converting enzyme(Rat)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50011190BDBM50011190(CHEMBL138409 | 5-tert-Butyl-3-[2-(1-carboxy-butyla...)
Affinity DataIC50: 0.600nMAssay Description:Compound was tested for inhibitory activity against angiotensin I converting enzymeMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAngiotensin-converting enzyme(Rat)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50051780BDBM50051780((2S,5R)-5-(2-Hydroxy-phenyl)-1-{2-[(S)-3-(4-hydrox...)
Affinity DataIC50: 0.600nMAssay Description:In vitro inhibition of rat angiotensin I converting enzymeMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/1/2012
Entry Details Article
PubMed
TargetAngiotensin-converting enzyme(Rat)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50011191BDBM50011191(CHEMBL139140 | 3-[6-Amino-2-(1-carboxy-3-phenyl-pr...)
Affinity DataIC50: 0.700nMAssay Description:Compound was tested for inhibitory activity against angiotensin I converting enzymeMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAngiotensin-converting enzyme(Rat)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50051791BDBM50051791((2S,5R)-5-(3-Hydroxy-phenyl)-1-{2-[(S)-3-(4-hydrox...)
Affinity DataIC50: 0.700nMAssay Description:In vitro inhibition of rat angiotensin I converting enzymeMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/1/2012
Entry Details Article
PubMedPDB3D3D Structure (crystal)
TargetAngiotensin-converting enzyme(Rat)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50050144BDBM50050144(1-[(S)-2-((S)-2-Mercapto-3-phenyl-propionylamino)-...)
Affinity DataIC50: 0.850nMAssay Description:Inhibitory activity against angiotensin I converting enzymeMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/3/2012
Entry Details Article
PubMed
TargetAngiotensin-converting enzyme(Rat)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50051803BDBM50051803((2S,5R)-1-{2-[3-(4-Chloro-phenyl)-2-mercapto-propi...)
Affinity DataIC50: 0.900nMAssay Description:In vitro inhibition of rat angiotensin I converting enzymeMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/1/2012
Entry Details Article
PubMed
TargetAngiotensin-converting enzyme(Rat)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50017122BDBM50017122(7-[2-(1-Carboxy-3-phenyl-propylamino)-propionyl]-1...)
Affinity DataIC50: 0.900nMAssay Description:Compound tested in vivo for inhibition of Angiotensin I converting enzyme in ratMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/19/2012
Entry Details Article
PubMed
TargetAngiotensin-converting enzyme(Rat)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50011192BDBM50011192(Vasotec | Vaseretic | (R)-1-[(S)-2-((S)-1-Carboxy-...)
Affinity DataIC50: 0.950nMAssay Description:Compound was tested for inhibitory activity against angiotensin I converting enzymeMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAngiotensin-converting enzyme(Rat)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50050125BDBM50050125(1-[(S)-2-((S)-2-Mercapto-3-phenyl-propionylamino)-...)
Affinity DataIC50: 1.10nMAssay Description:Inhibitory activity against angiotensin I converting enzymeMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/3/2012
Entry Details Article
PubMed
TargetAngiotensin-converting enzyme(Rat)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50011194BDBM50011194(CHEMBL423916 | 3-[2-(1-Carboxy-3-phenyl-propylamin...)
Affinity DataIC50: 1.5nMAssay Description:Compound was tested for inhibitory activity against angiotensin I converting enzymeMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAngiotensin-converting enzyme(Rat)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50051790BDBM50051790((2S,5R)-5-(3-Hydroxy-phenyl)-1-[2-((S)-2-mercapto-...)
Affinity DataIC50: 1.5nMAssay Description:In vitro inhibition of rat angiotensin I converting enzymeMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/1/2012
Entry Details Article
PubMed
TargetAngiotensin-converting enzyme(Rat)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50050162BDBM50050162((S)-3-(4-Hydroxy-phenyl)-2-[(S)-2-((S)-2-mercapto-...)
Affinity DataIC50: 1.5nMAssay Description:Inhibitory activity against angiotensin I converting enzymeMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/3/2012
Entry Details Article
PubMed
TargetAngiotensin-converting enzyme(Rat)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50287432BDBM50287432((S)-2-[(1-{Hydroxy-[(R)-1-(4-nitro-benzoylamino)-2...)
Affinity DataIC50: 1.5nMAssay Description:Compound was measured for the inhibition of Angiotensin I converting enzymeMore data for this Ligand-Target Pair
In Depth
Date in BDB:
9/26/2012
Entry Details Article

TargetAngiotensin-converting enzyme(Rat)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50050148BDBM50050148((S)-3-(4-Hydroxy-phenyl)-2-[(S)-2-((S)-2-mercapto-...)
Affinity DataIC50: 1.60nMAssay Description:Inhibitory activity against angiotensin I converting enzymeMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/3/2012
Entry Details Article
PubMed
TargetAngiotensin-converting enzyme(Rat)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50050136BDBM50050136(1-[(S)-2-((S)-2-Mercapto-3-phenyl-propionylamino)-...)
Affinity DataIC50: 1.60nMAssay Description:Inhibitory activity against angiotensin I converting enzymeMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/3/2012
Entry Details Article
PubMed
TargetAngiotensin-converting enzyme(Rat)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50050134BDBM50050134(1-[2-((S)-2-Mercapto-4-phenyl-butyrylamino)-2-meth...)
Affinity DataIC50: 1.60nMAssay Description:Inhibitory activity against angiotensin I converting enzymeMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/3/2012
Entry Details Article
PubMed
TargetAngiotensin-converting enzyme(Rat)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50050146BDBM50050146(1-[(2S,3R)-2-((S)-2-Mercapto-3-phenyl-propionylami...)
Affinity DataIC50: 1.70nMAssay Description:Inhibitory activity against angiotensin I converting enzymeMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/3/2012
Entry Details Article
PubMed
TargetAngiotensin-converting enzyme(Rat)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50021153BDBM50021153([(3S)-3-{[(1S)-1-(ethoxycarbonyl)-3-phenylpropyl]a...)
Affinity DataIC50: 1.70nMAssay Description:In vitro inhibitory activity against Angiotensin I converting enzymeMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/13/2012
Entry Details Article
PubMed
TargetAngiotensin-converting enzyme(Rat)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50021135BDBM50021135(CHEMBL36429 | 2-(1-Carboxymethyl-2-oxo-2,3,4,5-tet...)
Affinity DataIC50: 1.70nMAssay Description:Inhibition of Angiotensin I converting enzyme in ratMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/13/2012
Entry Details Article
PubMed
TargetAngiotensin-converting enzyme(Rat)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50369209BDBM50369209(CHEMBL1794012)
Affinity DataIC50: 1.90nMAssay Description:Inhibitory activity against angiotensin I converting enzymeMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/3/2012
Entry Details Article
PubMed
TargetAngiotensin-converting enzyme(Rat)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 21642BDBM21642((2S)-1-[(2S)-2-methyl-3-sulfanylpropanoyl]pyrrolid...)
Affinity DataKi:  2nMAssay Description:NEP was preincubated in black 96-well microplates with or without increasing concentrations of inhibitors. DGPA was added, and the reaction was stopp...More data for this Ligand-Target Pair
In Depth
Date in BDB:
4/19/2008
Entry Details Article
PubMed
TargetAngiotensin-converting enzyme(Rat)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50051799BDBM50051799((2S,5R)-1-{2-[(S)-2-Mercapto-3-(4-methoxy-phenyl)-...)
Affinity DataIC50: 2.20nMAssay Description:In vitro inhibition of rat angiotensin I converting enzymeMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/1/2012
Entry Details Article
PubMed
TargetAngiotensin-converting enzyme(Rat)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50367254BDBM50367254(ENALAPRILAT)
Affinity DataIC50: 2.30nMAssay Description:Inhibition of rat Angiotensin I converting enzyme (ACE), using Hip-Gly-Gly as synthetic substrate.More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/15/2012
Entry Details Article
PubMed
TargetAngiotensin-converting enzyme(Rat)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50226811BDBM50226811(CHEMBL3349972)
Affinity DataIC50: 2.40nMAssay Description:Inhibition of rat Angiotensin I converting enzyme (ACE), using Hip-Gly-Gly as synthetic substrate.More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/15/2012
Entry Details Article
PubMed
TargetAngiotensin-converting enzyme(Rat)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50051786BDBM50051786((2S,5R)-1-{2-[(S)-3-(4-Hydroxy-phenyl)-2-mercapto-...)
Affinity DataIC50: 2.5nMAssay Description:In vitro inhibition of rat angiotensin I converting enzymeMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/1/2012
Entry Details Article
PubMed
TargetAngiotensin-converting enzyme(Rat)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50287430BDBM50287430((S)-2-[(1-{[(R)-1-((S)-6-Amino-2-methanesulfonylam...)
Affinity DataIC50: 2.5nMAssay Description:Compound was measured for the inhibition of Angiotensin I converting enzymeMore data for this Ligand-Target Pair
In Depth
Date in BDB:
9/26/2012
Entry Details Article

TargetAngiotensin-converting enzyme(Rat)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50050143BDBM50050143((S)-3-(4-Hydroxy-phenyl)-2-[(2S,3S)-2-((S)-2-merca...)
Affinity DataIC50: 2.5nMAssay Description:Inhibitory activity against angiotensin I converting enzymeMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/3/2012
Entry Details Article
PubMed
TargetAngiotensin-converting enzyme(Rat)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50405541BDBM50405541(CHEMBL2079670)
Affinity DataIC50: 2.60nMAssay Description:Inhibition of rat Angiotensin I converting enzyme (ACE), using Hip-Gly-Gly as synthetic substrate.More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/15/2012
Entry Details Article
PubMed
TargetAngiotensin-converting enzyme(Rat)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50405179BDBM50405179(CHEMBL2114418)
Affinity DataIC50: 2.90nMAssay Description:Inhibition of Angiotensin I converting enzyme in ratMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/13/2012
Entry Details Article
PubMed
TargetAngiotensin-converting enzyme(Rat)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50050138BDBM50050138((S)-3-(4-Hydroxy-phenyl)-2-[(S)-2-((S)-2-mercapto-...)
Affinity DataIC50: 3nMAssay Description:Inhibitory activity against angiotensin I converting enzymeMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/3/2012
Entry Details Article
PubMed
TargetAngiotensin-converting enzyme(Rat)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 21642BDBM21642((2S)-1-[(2S)-2-methyl-3-sulfanylpropanoyl]pyrrolid...)
Affinity DataIC50: 3nMAssay Description:In vitro inhibitory activity against rat serum angiotensin I converting enzyme using hippuryl-glycyl-glycine as substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/26/2012
Entry Details Article
PubMed
TargetAngiotensin-converting enzyme(Rat)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50115837BDBM50115837(2-[2-(5-Cyano-indan-1-yl)-3-mercapto-propionylamin...)
Affinity DataKi:  3nMAssay Description:In vitro inhibition of Angiotensin I converting enzyme.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAngiotensin-converting enzyme(Rat)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50051778BDBM50051778((2S,5R)-1-[2-((S)-2-Mercapto-3-phenyl-propionylami...)
Affinity DataIC50: 3.10nMAssay Description:In vitro inhibition of rat angiotensin I converting enzymeMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/1/2012
Entry Details Article
PubMed
TargetAngiotensin-converting enzyme(Rat)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50051800BDBM50051800(1-{2-[(S)-3-(4-Hydroxy-phenyl)-2-mercapto-propiony...)
Affinity DataIC50: 3.10nMAssay Description:In vitro inhibition of rat angiotensin I converting enzymeMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/1/2012
Entry Details Article
PubMed
TargetAngiotensin-converting enzyme(Rat)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50027141BDBM50027141(1-(5-Benzoylamino-4-oxo-6-phenyl-hexanoyl)-pyrroli...)
Affinity DataIC50: 3.20nMAssay Description:Inhibition of rat Angiotensin I converting enzyme (ACE), using Hip-Gly-Gly as synthetic substrate.More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/15/2012
Entry Details Article
PubMed
TargetAngiotensin-converting enzyme(Rat)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50051795BDBM50051795((2S,5R)-5-(3-Hydroxy-phenyl)-1-{2-[(S)-3-(3-hydrox...)
Affinity DataIC50: 3.20nMAssay Description:In vitro inhibition of rat angiotensin I converting enzymeMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/1/2012
Entry Details Article
PubMed
TargetAngiotensin-converting enzyme(Rat)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 21642BDBM21642((2S)-1-[(2S)-2-methyl-3-sulfanylpropanoyl]pyrrolid...)
Affinity DataIC50: 3.20nMAssay Description:Inhibition of Wistar rat plasma angiotensin 1-converting enzyme using H-hippuryl-His-Leu-OH as substrate after 20 mins by fluorescence assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/29/2020
Entry Details Article
PubMed
TargetAngiotensin-converting enzyme(Rat)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50050133BDBM50050133(1-[(S)-2-((2S,3S)-2-Mercapto-3-methyl-pentanoylami...)
Affinity DataIC50: 3.30nMAssay Description:Inhibitory activity against angiotensin I converting enzymeMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/3/2012
Entry Details Article
PubMed
TargetAngiotensin-converting enzyme(Rat)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50051794BDBM50051794((2S,5R)-1-{2-[(S)-3-(4-Amino-phenyl)-2-mercapto-pr...)
Affinity DataIC50: 3.5nMAssay Description:In vitro inhibition of rat angiotensin I converting enzymeMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/1/2012
Entry Details Article
PubMed
TargetAngiotensin-converting enzyme(Rat)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50050145BDBM50050145((S)-3-(4-Hydroxy-phenyl)-2-[(2S,3S)-2-((S)-2-merca...)
Affinity DataIC50: 3.5nMAssay Description:Inhibitory activity against angiotensin I converting enzymeMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/3/2012
Entry Details Article
PubMed
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