| Reaction Details |
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 | Report a problem with these data |
| Target | HIV-1 protease |
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| Ligand | BDBM40774 |
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| Substrate/Competitor | n/a |
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| Meas. Tech. | Enzyme Inhibition Assay |
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| Ki | 3.8±0.0 nM |
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| Citation |  Chen, CA; Sieburth, SM; Glekas, A; Hewitt, GW; Trainor, GL; Erickson-Viitanen, S; Garber, SS; Cordova, B; Jeffry, S; Klabe, RM Drug design with a new transition state analog of the hydrated carbonyl: silicon-based inhibitors of the HIV protease. Chem Biol8:1161-6 (2001) [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 |
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| Synonyms: | HIV-1 protease wild type |
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| Type: | Protein |
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| Mol. Mass.: | 10757.68 |
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| Organism: | Human immunodeficiency virus |
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| Description: | O90785 |
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| Residue: | 99 |
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| Sequence: | PQITLWQRPLVTVKIGGQLREALLDTGADDTVLEDINLPGKWKPKMIGGIGGFIKVKQYE
QVLIEICGKKAIGTVLVGPTPVNIIGRNMLTQIGCTLNF
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| BDBM40774 |
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| n/a |
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| Name | BDBM40774 |
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| Synonyms: | Carbinol, 18b |
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| Type | Small organic molecule |
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| Emp. Form. | C39H42N2O5 |
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| Mol. Mass. | 618.7612 |
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| SMILES | OC(C[C@@H](Cc1ccccc1)C(=O)NC1C(O)Cc2ccccc12)C[C@@H](Cc1ccccc1)C(=O)NC1C(O)Cc2ccccc12 |r| |
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| Structure | 
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