Reaction Details |
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Target | Integrase |
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Ligand | BDBM50065794 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_90700 (CHEMBL702101) |
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IC50 | 114000±n/a nM |
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Citation | Mekouar, K; Mouscadet, JF; Desmaële, D; Subra, F; Leh, H; Savouré, D; Auclair, C; d'Angelo, J Styrylquinoline derivatives: a new class of potent HIV-1 integrase inhibitors that block HIV-1 replication in CEM cells. J Med Chem41:2846-57 (1998) [PubMed] Article |
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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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BDBM50065794 |
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n/a |
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Name | BDBM50065794 |
Synonyms: | 8-Hydroxy-2-methyl-quinoline-7-carboxylic acid | 8-hydroxy-2-methylquinoline-7-carboxylic acid | CHEMBL39823 |
Type | Small organic molecule |
Emp. Form. | C11H9NO3 |
Mol. Mass. | 203.1941 |
SMILES | Cc1ccc2ccc(C(O)=O)c(O)c2n1 |
Structure |
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