BDBM12913 (5S)-N-[(1S,2R)-1-Benzyl-2-hydroxy-3-[[(3-methoxyphenyl)-sulfonyl][(R)-(tetrahydro-2-furanyl)methyl]amino]propyl]-2-oxo-3-phenyloxazolidine-5-carboxamide::(5S)-N-[(2S,3R)-3-hydroxy-4-[(3-methoxybenzene)[(2R)-oxolan-2-ylmethyl]sulfonamido]-1-phenylbutan-2-yl]-2-oxo-3-phenyl-1,3-oxazolidine-5-carboxamide::N-Aryl-oxazolidinone-5-carboxamide Analogue 39a

SMILES COc1cccc(c1)S(=O)(=O)N(C[C@@H](O)[C@H](Cc1ccccc1)NC(=O)[C@@H]1CN(C(=O)O1)c1ccccc1)C[C@H]1CCCO1

InChI Key InChIKey=BKVPEHBIRUOJPV-SFGWMHHMSA-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 = 12913   

TargetDimer of Gag-Pol polyprotein [491-589,Q496K](Human immunodeficiency virus type 1)
University of Massachusetts Medical School

LigandPNGBDBM12913((5S)-N-[(1S,2R)-1-Benzyl-2-hydroxy-3-[[(3-methoxyp...)
Affinity DataKi:  42nMAssay Description:HIV-1 protease inhibitor activities were determined by the fluorescence resonance energy transfer (FRET) method. The energy transfer donor (EDANS) an...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHIV-1 protease(Human immunodeficiency virus)
Umbi

Curated by ChEMBL
LigandPNGBDBM12913((5S)-N-[(1S,2R)-1-Benzyl-2-hydroxy-3-[[(3-methoxyp...)
Affinity DataKi:  42nMAssay Description:Inhibition of HIV1 protease Q7K mutant by FRET methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHIV-1 protease(Human immunodeficiency virus)
Umbi

Curated by ChEMBL
LigandPNGBDBM12913((5S)-N-[(1S,2R)-1-Benzyl-2-hydroxy-3-[[(3-methoxyp...)
Affinity DataKi:  42nMAssay Description:Inhibition of HIV1 protease Q7K mutant by FRET methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed