Reaction Details Report a problem with these data
Target
Integrase
Ligand
BDBM50051643
Substrate
n/a
Meas. Tech.
ChEMBL_90721 (CHEMBL701114)
IC50
78000±n/a nM
Citation
 Mazumder, A; Wang, S; Neamati, N; Nicklaus, M; Sunder, S; Chen, J; Milne, GW; Rice, WG; Burke, TR; Pommier, Y Antiretroviral agents as inhibitors of both human immunodeficiency virus type 1 integrase and protease. J Med Chem 39:2472-81 (1996) [PubMed]  Article 
Target
Name:
Integrase
Synonyms:
Human immunodeficiency virus type 1 integrase
Type:
PROTEIN
Mol. Mass.:
32231.48
Organism:
Human immunodeficiency virus 1
Description:
ChEMBL_90865
Residue:
288
Sequence:
FLDGIDKAQDEHEKYHSNWRAMASDFNLPPVVAKEIVASCDKCQLKGEAMHGQVDCSPGIWQLDCTHLEGKVILVAVHVASGYIEAEVIPAETGQETAYFLLKLAGRWPVKTIHTDNGSNFTSTTVKAACWWAGIKQEFGIPYNPQSQGVVESMNKELKKIIGQVRDQAEHLKTAVQMAVFIHNFKRKGGIGGYSAGERIVDIIATDIQTKELQKQITKIQNFRVYYRDSRDPLWKGPAKLLWKGEGAVVIQDNSDIKVVPRRKVKIIRDYGKQMAGDDCVASRQDED
  
Inhibitor
Name:
BDBM50051643
Synonyms:
CHEMBL309934 | N-{4-[Bis-(3-hydroxy-1,4-dioxo-1,4-dihydro-naphthalen-2-yl)-methyl]-phenyl}-acetamide | NSC-117276
Type:
Small organic molecule
Emp. Form.:
C29H19NO7
Mol. Mass.:
493.4637
SMILES:
CC(=O)Nc1ccc(cc1)C(=C1C(=O)C(=O)c2ccccc2C1=O)c1c(O)c(O)c2ccccc2c1O |w:10.26|
Structure:
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