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TargetIntegrase
LigandBDBM50187771
Substrate/Competitorn/a
Meas. Tech.ChEMBL_378127 (CHEMBL869776)
IC50 7.2±n/a nM
Citation Metobo, SEJin, HTsiang, MKim, CU Design, synthesis, and biological evaluation of novel tricyclic HIV-1 integrase inhibitors by modification of its pyridine ring. Bioorg Med Chem Lett16:3985-8 (2006) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Integrase
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:
FLDGIDKAQDEHEKYHSNWRAMASDFNLPPVVAKEIVASCDKCQLKGEAMHGQVDCSPGI
WQLDCTHLEGKVILVAVHVASGYIEAEVIPAETGQETAYFLLKLAGRWPVKTIHTDNGSN
FTSTTVKAACWWAGIKQEFGIPYNPQSQGVVESMNKELKKIIGQVRDQAEHLKTAVQMAV
FIHNFKRKGGIGGYSAGERIVDIIATDIQTKELQKQITKIQNFRVYYRDSRDPLWKGPAK
LLWKGEGAVVIQDNSDIKVVPRRKVKIIRDYGKQMAGDDCVASRQDED
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BDBM50187771
n/a
NameBDBM50187771
Synonyms:7-(4-fluorobenzyl)-3-fluoro-9-hydroxy-5-methoxy-6,7-dihydropyrrolo[3,4-g]quinolin-8-one | CHEMBL212213
TypeSmall organic molecule
Emp. Form.C19H14F2N2O3
Mol. Mass.356.3229
SMILESCOc1c2CN(Cc3ccc(F)cc3)C(=O)c2c(O)c2ncc(F)cc12
Structure
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