| Literature DB >> 22677312 |
Jason N Mock1, John P Taliaferro, Xiao Lu, Sravan Kumar Patel, Brian S Cummings, Timothy E Long.
Abstract
Haloenol pyran-2-ones and morpholin-2-ones were synthesized and evaluated as inhibitors of cell growth in two different prostate human cancer cell lines (PC-3 and LNCaP). Analogs derived from L- and D-phenylglycine were found to be the most effective antagonists of LNCaP and PC-3 cell growth. Additional studies reveal that the inhibitors induced G2/M arrest and the (S)-enantiomer of the phenylglycine-based derivatives was a more potent inhibitor of cytosolic iPLA(2)β. Published by Elsevier Ltd.Entities:
Mesh:
Substances:
Year: 2012 PMID: 22677312 PMCID: PMC3376906 DOI: 10.1016/j.bmcl.2012.05.038
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823