Reaction Details |
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Target | Integrase |
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Ligand | BDBM23402 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_378064 (CHEMBL869770) |
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IC50 | 50±n/a nM |
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Citation | Jin, H; Cai, RZ; Schacherer, L; Jabri, S; Tsiang, M; Fardis, M; Chen, X; Chen, JM; Kim, CU Design, synthesis, and SAR studies of novel and highly active tri-cyclic HIV integrase inhibitors. Bioorg Med Chem Lett16:3989-92 (2006) [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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BDBM23402 |
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n/a |
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Name | BDBM23402 |
Synonyms: | 5-(1,1-dioxo-1,2-thiazinan-2-yl)-N-[(4-fluorophenyl)methyl]-8-hydroxy-1,6-naphthyridine-7-carboxamide | CHEMBL414850 | L-870,810 |
Type | Small organic molecule |
Emp. Form. | C20H19FN4O4S |
Mol. Mass. | 430.453 |
SMILES | Oc1c(nc(N2CCCCS2(=O)=O)c2cccnc12)C(=O)NCc1ccc(F)cc1 |
Structure |
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