| Literature DB >> 27994761 |
Yuzhi Lu1, Shuangchan Wu1, Yuan Yue1, Si He1, Jun Li1, Jun Tang1, Wei Wang1, Hai-Bing Zhou1.
Abstract
A series of gossypol Schiff bases that were derived from unnatural linear amino acid methyl esters were identified and found to be much more potent than gossypol and ABT-199 in terms of anticancer activity. This is the first example of gossypol Schiff bases with increased activity. The investigation of the Schiff base side chain of gossypol revealed that the unique anticancer effect was achieved by the introduction of hydrophobic ester groups. The optimized products showed low micromolar pan antitumor activities against NCI-60 tumor cell lines, which is promising for further drug development. Studies on the preliminary mechanism of action for their cellular activities was also carried out with antiapoptotic protein (Bcl-2 and Mcl-1) inhibition FP assays. The molecular modeling analysis demonstrated a possible binding mode for these compounds with Bcl-2, which could explain the binding affinity of the novel gossypol Schiff bases with these proteins.Entities:
Keywords: Gossypol Schiff bases; antiapoptotic proteins; linear amino acid esters
Year: 2016 PMID: 27994761 PMCID: PMC5150665 DOI: 10.1021/acsmedchemlett.6b00302
Source DB: PubMed Journal: ACS Med Chem Lett ISSN: 1948-5875 Impact factor: 4.345