BDBM50115843 (2S)-2-[(2R)-2-[(1R)-5-bromo-2,3-dihydro-1H-inden-1-yl]-3-sulfanylpropanamido]-3-(1H-indol-3-yl)propanoic acid::CHEMBL301646

SMILES OC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](CS)[C@H]1CCc2cc(Br)ccc12

InChI Key InChIKey=STCPANYJWPVHTG-ZVDOUQERSA-N

Data  3 KI

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50115843   

TargetNeprilysin(Oryctolagus cuniculus (rabbit))
University Of Paris

Curated by ChEMBL
LigandPNGBDBM50115843((2S)-2-[(2R)-2-[(1R)-5-bromo-2,3-dihydro-1H-inden-...)
Affinity DataKi:  1.80nMAssay Description:In vitro inhibition of Neutral endopeptidase.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetEndothelin-converting enzyme 1(Homo sapiens (Human))
University Of Paris

Curated by ChEMBL
LigandPNGBDBM50115843((2S)-2-[(2R)-2-[(1R)-5-bromo-2,3-dihydro-1H-inden-...)
Affinity DataKi:  18nMAssay Description:In vitro inhibition of endothelin converting enzyme.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAngiotensin-converting enzyme(Rattus norvegicus)
University Of Paris

Curated by ChEMBL
LigandPNGBDBM50115843((2S)-2-[(2R)-2-[(1R)-5-bromo-2,3-dihydro-1H-inden-...)
Affinity DataKi:  55nMAssay Description:In vitro inhibition of Angiotensin I converting enzyme.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed