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TargetHIV-1 protease
LigandBDBM93237
Substrate/Competitorn/a
Meas. Tech.Fluorometric Assay
Ki 20±0.0 nM
Citation Wannberg, JKaiser, NFVrang, LSamuelsson, BLarhed, MHallberg, A High-speed synthesis of potent C2-symmetric HIV-1 protease inhibitors by in-situ aminocarbonylations. J Comb Chem7:611-7 (2005) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
HIV-1 protease
Name:HIV-1 protease
Synonyms:n/a
Type:Protein
Mol. Mass.:10794.16
Organism:Human immunodeficiency virus
Description:Q9YQ34
Residue:99
Sequence:
PQITLWQRPLVTVKIGGQLKEALLDTGADDTVLEEMNLPGRWKPKMIGGIGGFIKVRQYD
QILVEICGHKAIGTVLVGPTPVNIIGRNLLTQIGCTLNF
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BDBM93237
n/a
NameBDBM93237
Synonyms:HIV-1 Protease Inhibitor, 6h
TypeSmall molecule
Emp. Form.C46H56N6O10
Mol. Mass.852.971
SMILESCNC(=O)[C@@H](NC(=O)[C@H](OCc1ccccc1C(=O)Nc1ccccc1)[C@H](O)[C@@H](O)[C@@H](OCc1ccccc1C(=O)Nc1ccccc1)C(=O)N[C@@H](C(C)C)C(=O)NC)C(C)C |r|
Structure
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