Reaction Details |
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Target | HIV-1 protease |
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Ligand | BDBM93238 |
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Substrate/Competitor | n/a |
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Meas. Tech. | Fluorometric Assay |
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Ki | 118±0.0 nM |
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Citation | Wannberg, J; Kaiser, NF; Vrang, L; Samuelsson, B; Larhed, M; Hallberg, A High-speed synthesis of potent C2-symmetric HIV-1 protease inhibitors by in-situ aminocarbonylations. J Comb Chem7:611-7 (2005) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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HIV-1 protease |
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Name: | HIV-1 protease |
Synonyms: | n/a |
Type: | Protein |
Mol. Mass.: | 10794.16 |
Organism: | Human immunodeficiency virus |
Description: | Q9YQ34 |
Residue: | 99 |
Sequence: | PQITLWQRPLVTVKIGGQLKEALLDTGADDTVLEEMNLPGRWKPKMIGGIGGFIKVRQYD
QILVEICGHKAIGTVLVGPTPVNIIGRNLLTQIGCTLNF
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BDBM93238 |
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n/a |
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Name | BDBM93238 |
Synonyms: | HIV-1 Protease Inhibitor, 6i |
Type | Small molecule |
Emp. Form. | C44H54N8O10 |
Mol. Mass. | 854.9472 |
SMILES | CNC(=O)[C@@H](NC(=O)[C@H](OCc1ccccc1C(=O)Nc1cccnc1)[C@H](O)[C@@H](O)[C@@H](OCc1ccccc1C(=O)Nc1cccnc1)C(=O)N[C@@H](C(C)C)C(=O)NC)C(C)C |r| |
Structure |
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