Reaction Details |
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Target | Gag-Pol polyprotein [489-587] |
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Ligand | BDBM50005688 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_157548 (CHEMBL763135) |
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Ki | 0.400000±n/a nM |
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Citation | Tam, TF; Carrière, J; MacDonald, D; Castelhano, AL; Pliura, DH; Dewdney, NJ; Thomas, EM; Bach, C; Barnett, J; Chan, H Intriguing structure-activity relations underlie the potent inhibition of HIV protease by norstatine-based peptides. J Med Chem35:1318-20 (1992) [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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BDBM50005688 |
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n/a |
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Name | BDBM50005688 |
Synonyms: | CHEMBL3085518 | N*1*-[1-Benzyl-3-(2-tert-butylcarbamoyl-pyrrolidin-1-yl)-2-hydroxy-3-oxo-propyl]-2-[2-(naphthalen-1-yloxy)-acetylamino]-succinamide |
Type | Small organic molecule |
Emp. Form. | C35H43N5O7 |
Mol. Mass. | 645.7452 |
SMILES | CC(C)(C)NC(=O)[C@@H]1CCCN1C(=O)[C@@H](O)[C@H](Cc1ccccc1)NC(=O)[C@H](CC(N)=O)NC(=O)COc1cccc2ccccc12 |
Structure |
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