Reaction Details |
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Target | Integrase |
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Ligand | BDBM50087432 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_90731 (CHEMBL701283) |
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IC50 | 1700±n/a nM |
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Citation | Zouhiri, F; Mouscadet, JF; Mekouar, K; Desmaële, D; Savouré, D; Leh, H; Subra, F; Le Bret, M; Auclair, C; d'Angelo, J Structure-activity relationships and binding mode of styrylquinolines as potent inhibitors of HIV-1 integrase and replication of HIV-1 in cell culture. J Med Chem43:1533-40 (2000) [PubMed] |
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More Info.: | Get all data from this article, Assay Method |
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Integrase |
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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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BDBM50087432 |
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n/a |
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Name | BDBM50087432 |
Synonyms: | 8-Hydroxy-2-[2-(4-nitro-phenyl)-vinyl]-quinoline-7-carboxylic acid | 8-hydroxy-2-(4-nitrostyryl)quinoline-7-carboxylic acid | CHEMBL431508 |
Type | Small organic molecule |
Emp. Form. | C18H12N2O5 |
Mol. Mass. | 336.2983 |
SMILES | OC(=O)c1ccc2ccc(\C=C\c3ccc(cc3)[N+]([O-])=O)nc2c1O |
Structure |
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