Reaction Details |
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Target | Gag-Pol polyprotein [489-587] |
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Ligand | BDBM50040573 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_159442 (CHEMBL763238) |
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IC50 | 20000±n/a nM |
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Citation | De Voss, JJ; Sui, Z; DeCamp, DL; Salto, R; Babé, LM; Craik, CS; Ortiz de Montellano, PR Haloperidol-based irreversible inhibitors of the HIV-1 and HIV-2 proteases. J Med Chem37:665-73 (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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BDBM50040573 |
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n/a |
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Name | BDBM50040573 |
Synonyms: | 4-[4-(4-Chloro-phenyl)-4-hydroxy-piperidin-1-yl]-1-phenyl-but-2-yn-1-one | CHEMBL161488 |
Type | Small organic molecule |
Emp. Form. | C21H20ClNO2 |
Mol. Mass. | 353.842 |
SMILES | OC1(CCN(CC#CC(=O)c2ccccc2)CC1)c1ccc(Cl)cc1 |
Structure |
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