| Literature DB >> 25897791 |
Konrad Hohlfeld1, Jörg Kurt Wegner2, Bart Kesteleyn2, Bruno Linclau1, Johan Unge3.
Abstract
A series of darunavir analogues featuring a substituted bis-THF ring as P2 ligand have been synthesized and evaluated. Very high affinity protease inhibitors (PIs) with an interesting activity on wild-type HIV and a panel of multi-PI resistant HIV-1 mutants containing clinically observed, primary mutations were identified using a cell-based assay. Crystal structure analysis was conducted on a number of PI analogues in complex with HIV-1 protease.Entities:
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Year: 2015 PMID: 25897791 DOI: 10.1021/acs.jmedchem.5b00358
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446