Reaction Details |
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Target | Integrase |
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Ligand | BDBM50157832 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1720244 (CHEMBL4135244) |
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IC50 | 35000±n/a nM |
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Citation | Kankanala, J; Kirby, KA; Huber, AD; Casey, MC; Wilson, DJ; Sarafianos, SG; Wang, Z Design, synthesis and biological evaluations of N-Hydroxy thienopyrimidine-2,4-diones as inhibitors of HIV reverse transcriptase-associated RNase H. Eur J Med Chem141:149-161 (2017) [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: | pol |
Type: | PROTEIN |
Mol. Mass.: | 32203.43 |
Organism: | Human immunodeficiency virus 1 |
Description: | ChEMBL_106649 |
Residue: | 288 |
Sequence: | FLDGIDKAQEEHEKYHSNWRAMASDFNLPPVVAKEIVASCDKCQLKGEAMHGQVDCSPGI
WQLDCTHLEGKVILVAVHVASGYIEAEVIPAETGQETAYFLLKLAGRWPVKTVHTDNGSN
FTSTTVKAACWWAGIKQEFGIPYNPQSQGVIESMNKELKKIIGQVRDQAEHLKTAVQMAV
FIHNFKRKGGIGGYSAGERIVDIIATDIQTKELQKQITKIQNFRVYYRDSRDPVWKGPAK
LLWKGEGAVVIQDNSDIKVVPRRKAKIIRDYGKQMAGDDCVASRQDED
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BDBM50157832 |
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n/a |
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Name | BDBM50157832 |
Synonyms: | 3-Hydroxy-4a,7a-dihydro-1H-thieno[2,3-d]pyrimidine-2,4-dione | CHEMBL361350 |
Type | Small organic molecule |
Emp. Form. | C6H4N2O3S |
Mol. Mass. | 184.173 |
SMILES | On1c(=O)[nH]c2sccc2c1=O |
Structure |
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