BDBM7982 (3S,4S)-5-[(4-bromophenyl)methoxy]-3-hydroxy-4-[(2S)-3-methyl-2-(pyridin-2-ylformamido)butanamido]-N-[2-(phenylamino)ethyl]pentanamide::Pyridine-2-carboxylic Acid {(S)-1-[(1S,2S)-1-(4-Bromobenzyloxymethyl)-2-hydroxy-3-(2-phenylaminoethylcarbamoyl)propylcarbamoyl]-2-methylpropyl}amide::Statine-like inhibitor 21

SMILES CC(C)[C@H](NC(=O)c1ccccn1)C(=O)N[C@@H](COCc1ccc(Br)cc1)[C@@H](O)CC(=O)NCCNc1ccccc1

InChI Key InChIKey=JVFUMKPBUZXHML-YCVJPRETSA-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 = 7982   

TargetPlasmepsin I(Plasmodium falciparum)
Linkoping University

LigandPNGBDBM7982((3S,4S)-5-[(4-bromophenyl)methoxy]-3-hydroxy-4-[(2...)
Affinity DataKi:  8.90nMAssay Description:Enzyme activities were assayed by monitoring the hydrolysis of substrate in the presence or absence of inhibitor compounds. The hydrolysis was record...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPlasmepsin II(Plasmodium falciparum)
Linkoping University

LigandPNGBDBM7982((3S,4S)-5-[(4-bromophenyl)methoxy]-3-hydroxy-4-[(2...)
Affinity DataKi:  74nM ΔG°:  -9.62kcal/molepH: 4.5 T: 2°CAssay Description:Enzyme activities were assayed by monitoring the hydrolysis of substrate in the presence or absence of inhibitor compounds. The hydrolysis was record...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin D(Homo sapiens (Human))
Linkoping University

LigandPNGBDBM7982((3S,4S)-5-[(4-bromophenyl)methoxy]-3-hydroxy-4-[(2...)
Affinity DataKi:  265nMAssay Description:Enzyme activities were assayed by monitoring the hydrolysis of substrate in the presence or absence of inhibitor compounds. The hydrolysis was record...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed