Reaction Details |
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Target | Protease |
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Ligand | BDBM50485786 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_858545 (CHEMBL2169549) |
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Ki | 700±n/a nM |
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Citation | Dufau, L; Marques Ressurreição, AS; Fanelli, R; Kihal, N; Vidu, A; Milcent, T; Soulier, JL; Rodrigo, J; Desvergne, A; Leblanc, K; Bernadat, G; Crousse, B; Reboud-Ravaux, M; Ongeri, S Carbonylhydrazide-based molecular tongs inhibit wild-type and mutated HIV-1 protease dimerization. J Med Chem55:6762-75 (2012) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Protease |
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Name: | Protease |
Synonyms: | n/a |
Type: | Enzyme |
Mol. Mass.: | 10904.79 |
Organism: | Human immunodeficiency virus 1 (HIV-1) |
Description: | Q9YQ12 |
Residue: | 99 |
Sequence: | PQITLWQRPFVTIKIEGQLKEALLDTGADDTVLEEMNLPGRWKPKMIGGIGGFIKVRQYD
QIVIEICGKKAIGTVLVGPTPVNIIGRNLLTQIGCTLNF
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BDBM50485786 |
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n/a |
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Name | BDBM50485786 |
Synonyms: | CHEMBL2164074 |
Type | Small organic molecule |
Emp. Form. | C32H48N12O10 |
Mol. Mass. | 760.7979 |
SMILES | CC(C)[C@H](NC(=O)NNC(=O)NNC(=O)CCCOc1ccc2ccc(OCCCC(=O)NNC(=O)NNC(=O)N[C@@H](C(C)C)C(N)=O)cc2c1)C(N)=O |r| |
Structure |
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