Reaction Details |
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Target | Gag-Pol polyprotein [489-587] |
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Ligand | BDBM50062941 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_159631 (CHEMBL881815) |
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IC50 | 1.9±n/a nM |
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Citation | Kempf, DJ; Sham, HL; Marsh, KC; Flentge, CA; Betebenner, D; Green, BE; McDonald, E; Vasavanonda, S; Saldivar, A; Wideburg, NE; Kati, WM; Ruiz, L; Zhao, C; Fino, L; Patterson, J; Molla, A; Plattner, JJ; Norbeck, DW Discovery of ritonavir, a potent inhibitor of HIV protease with high oral bioavailability and clinical efficacy. J Med Chem41:602-17 (1998) [PubMed] Article |
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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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BDBM50062941 |
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n/a |
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Name | BDBM50062941 |
Synonyms: | ((1S,3S,4S)-1-Benzyl-4-{2-[3-cyclopropyl-3-(2-isopropyl-thiazol-4-ylmethyl)-ureido]-3-methyl-butyrylamino}-3-hydroxy-5-phenyl-pentyl)-carbamic acid thiazol-5-ylmethyl ester | CHEMBL348147 |
Type | Small organic molecule |
Emp. Form. | C39H50N6O5S2 |
Mol. Mass. | 746.982 |
SMILES | CC(C)C(NC(=O)N(Cc1csc(n1)C(C)C)C1CC1)C(=O)N[C@@H](Cc1ccccc1)[C@@H](O)C[C@H](Cc1ccccc1)NC(=O)OCc1cncs1 |
Structure |
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