Reaction Details |
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Target | Gag-Pol polyprotein [489-587] |
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Ligand | BDBM50200956 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_422734 (CHEMBL854830) |
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Ki | 14±n/a nM |
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Citation | Whiting, M; Tripp, JC; Lin, YC; Lindstrom, W; Olson, AJ; Elder, JH; Sharpless, KB; Fokin, VV Rapid discovery and structure-activity profiling of novel inhibitors of human immunodeficiency virus type 1 protease enabled by the copper(I)-catalyzed synthesis of 1,2,3-triazoles and their further functionalization. J Med Chem49:7697-710 (2006) [PubMed] Article |
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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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BDBM50200956 |
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n/a |
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Name | BDBM50200956 |
Synonyms: | CHEMBL262496 | cyclopentyl (2S,3S)-3-[4-([4-(2,5-dimethylphenyl)piperazin-1-yl]methyl)-5-(hydroxymethyl)-1H-1,2,3-triazol-1-yl]-1,4-diphenylbutan-2-ylcarbamate |
Type | Small organic molecule |
Emp. Form. | C38H48N6O3 |
Mol. Mass. | 636.8261 |
SMILES | Cc1ccc(C)c(c1)N1CCN(Cc2nnn([C@@H](Cc3ccccc3)[C@H](Cc3ccccc3)NC(=O)OC3CCCC3)c2CO)CC1 |r| |
Structure |
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