| Reaction Details |
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 | Report a problem with these data |
| Target | Protease |
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| Ligand | BDBM50484743 |
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| Substrate/Competitor | n/a |
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| Meas. Tech. | ChEMBL_807276 (CHEMBL1960369) |
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| Ki | 3.8±n/a nM |
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| Citation |  Yan, J; Huang, N; Li, S; Yang, LM; Xing, W; Zheng, YT; Hu, Y Synthesis and biological evaluation of novel amprenavir-based P1-substituted bi-aryl derivatives as ultra-potent HIV-1 protease inhibitors. Bioorg Med Chem Lett22:1976-9 (2012) [PubMed] Article |
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| More Info.: | Get all data from this article, Assay Method |
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| Protease |
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| Name: | Protease |
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| Synonyms: | n/a |
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| Type: | Enzyme |
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| Mol. Mass.: | 10904.79 |
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| Organism: | Human immunodeficiency virus 1 (HIV-1) |
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| Description: | Q9YQ12 |
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| Residue: | 99 |
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| Sequence: | PQITLWQRPFVTIKIEGQLKEALLDTGADDTVLEEMNLPGRWKPKMIGGIGGFIKVRQYD
QIVIEICGKKAIGTVLVGPTPVNIIGRNLLTQIGCTLNF
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| BDBM50484743 |
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| n/a |
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| Name | BDBM50484743 |
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| Synonyms: | CHEMBL1957074 |
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| Type | Small organic molecule |
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| Emp. Form. | C31H39N3O7S |
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| Mol. Mass. | 597.722 |
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| SMILES | COc1ccc(cc1)S(=O)(=O)N(CC(C)C)C[C@@H](O)[C@H](Cc1ccc(cc1)-c1ccncc1)NC(=O)O[C@H]1CCOC1 |r| |
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| Structure | 
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