Reaction Details |
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Target | Integrase |
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Ligand | BDBM50115581 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_88608 (CHEMBL873101) |
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IC50 | >100000±n/a nM |
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Citation | Pais, GC; Zhang, X; Marchand, C; Neamati, N; Cowansage, K; Svarovskaia, ES; Pathak, VK; Tang, Y; Nicklaus, M; Pommier, Y; Burke, TR Structure activity of 3-aryl-1,3-diketo-containing compounds as HIV-1 integrase inhibitors. J Med Chem45:3184-94 (2002) [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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BDBM50115581 |
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n/a |
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Name | BDBM50115581 |
Synonyms: | (Z)-2-Hydroxy-4-oxo-4-(4-phenoxy-phenyl)-but-2-enoic acid | 2-Hydroxy-4-oxo-4-(4-phenoxy-phenyl)-but-2-enoic acid | CHEMBL108423 | CHEMBL185721 | CHEMBL573638 |
Type | Small organic molecule |
Emp. Form. | C16H12O5 |
Mol. Mass. | 284.2635 |
SMILES | OC(=O)C(=O)CC(=O)c1ccc(Oc2ccccc2)cc1 |
Structure |
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