Reaction Details |
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Target | HIV-1 protease |
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Ligand | BDBM50480933 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_594352 (CHEMBL1048550) |
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Ki | 16±n/a nM |
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Citation | Mahalingam, AK; Axelsson, L; Ekegren, JK; Wannberg, J; Kihlström, J; Unge, T; Wallberg, H; Samuelsson, B; Larhed, M; Hallberg, A HIV-1 protease inhibitors with a transition-state mimic comprising a tertiary alcohol: improved antiviral activity in cells. J Med Chem53:607-15 (2010) [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 |
Synonyms: | HIV-1 | HIV-1 protease | protease |
Type: | PROTEIN |
Mol. Mass.: | 10795.19 |
Organism: | Human immunodeficiency virus |
Description: | ChEMBL_118439 |
Residue: | 99 |
Sequence: | PQVTLWQRPLVTIKIGGQLKEALLDTGADDTVLEEMSLPGRWKPKMIGGIGGFIKVRQYD
QILIEICGHKAIGTVLIGPTPVNIIGRNLLTQIGCTLNF
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BDBM50480933 |
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n/a |
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Name | BDBM50480933 |
Synonyms: | CHEMBL583370 |
Type | Small organic molecule |
Emp. Form. | C40H47N5O6 |
Mol. Mass. | 693.8311 |
SMILES | COC(=O)N[C@H](C(=O)NN(CC[C@@](O)(Cc1ccccc1)C(=O)N[C@@H]1[C@H](O)Cc2ccccc12)Cc1ccc(cc1)-c1ccccn1)C(C)(C)C |r| |
Structure |
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