Reaction Details |
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Target | Gag-Pol polyprotein [489-587] |
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Ligand | BDBM50037838 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_159307 (CHEMBL769360) |
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IC50 | >35000±n/a nM |
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Citation | Kitchin, J; Bethell, RC; Cammack, N; Dolan, S; Evans, DN; Holman, S; Holmes, DS; McMeekin, P; Mo, CL; Nieland, N Synthesis and structure-activity relationships of a series of penicillin-derived HIV proteinase inhibitors: heterocyclic ring systems containing P1' and P2' substituents. J Med Chem37:3707-16 (1994) [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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BDBM50037838 |
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n/a |
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Name | BDBM50037838 |
Synonyms: | (2R,4S)-2-[Benzylcarbamoyl-((S)-phenylacetylamino)-methyl]-5,5-dimethyl-thiazolidine-4-carboxylic acid [(S)-3-((2S,4R)-2-tert-butylcarbamoyl-4-ethoxy-pyrrolidin-1-yl)-2-hydroxy-propyl]-amide | CHEMBL332736 |
Type | Small organic molecule |
Emp. Form. | C37H54N6O6S |
Mol. Mass. | 710.926 |
SMILES | CCO[C@@H]1C[C@H](N(C[C@@H](O)CNC(=O)[C@@H]2N[C@H](SC2(C)C)C(NC(=O)Cc2ccccc2)C(=O)NCc2ccccc2)C1)C(=O)NC(C)(C)C |
Structure |
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