Reaction Details |
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Target | Gag-Pol polyprotein [489-587] |
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Ligand | BDBM50102274 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_196188 (CHEMBL801175) |
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Ki | 800±n/a nM |
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Citation | Campiani, G; Aiello, F; Fabbrini, M; Morelli, E; Ramunno, A; Armaroli, S; Nacci, V; Garofalo, A; Greco, G; Novellino, E; Maga, G; Spadari, S; Bergamini, A; Ventura, L; Bongiovanni, B; Capozzi, M; Bolacchi, F; Marini, S; Coletta, M; Guiso, G; Caccia, S Quinoxalinylethylpyridylthioureas (QXPTs) as potent non-nucleoside HIV-1 reverse transcriptase (RT) inhibitors. Further SAR studies and identification of a novel orally bioavailable hydrazine-based antiviral agent. J Med Chem44:305-15 (2001) [PubMed] |
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More Info.: | Get all data from this article, Assay Method |
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Gag-Pol polyprotein [489-587] |
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Name: | Gag-Pol polyprotein [489-587] |
Synonyms: | Human immunodeficiency virus type 1 protease | POL_HV1H2 | Pol polyprotein | gag-pol |
Type: | Enzyme Subunit |
Mol. Mass.: | 10781.16 |
Organism: | Human immunodeficiency virus type 1 |
Description: | P04585[489-587] |
Residue: | 99 |
Sequence: | PQVTLWQRPLVTIKIGGQLKEALLDTGADDTVLEEMSLPGRWKPKMIGGIGGFIKVRQYD
QILIEICGHKAIGTVLVGPTPVNIIGRNLLTQIGCTLNF
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BDBM50102274 |
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n/a |
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Name | BDBM50102274 |
Synonyms: | 1-(5-Bromo-pyridin-2-yl)-3-[2-(7,8-dimethyl-pyrrolo[1,2-a]quinoxalin-4-yloxy)-ethyl]-thiourea | CHEMBL317406 |
Type | Small organic molecule |
Emp. Form. | C21H20BrN5OS |
Mol. Mass. | 470.385 |
SMILES | Cc1cc2nc(OCCNC(=S)Nc3ccc(Br)cn3)c3cccn3c2cc1C |
Structure |
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