Design, synthesis and structure-activity study of shorter hexa peptide analogues as HIV-1 protease inhibitors
Bioorg Med Chem 16(2):7 (2008) PMID 17981043
The design, synthesis and HIV-1 protease inhibition of the shorter synthetic hexa peptides are discussed. Leu-Leu-Glu-Tyr-Val-Xaa. Where, Xaa=Phe, Met, Tyr or Trp.
DOI: 10.1016/j.bmc.2007.10.052
Version: za2963e q8za0 q8zb5 q8zcf q8zd8 q8zef q8zf4 q8zgf