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Title: Expedient synthesis and structure-activity relationships of phenanthroindolizidine and phenanthroquinolizidine alkaloids. Author: Chuang TH, Lee SJ, Yang CW, Wu PL. Journal: Org Biomol Chem; 2006 Mar 07; 4(5):860-7. PubMed ID: 16493470. Abstract: The total synthesis of alkaloids phenanthroindolizidine 1a, tylophorine 1b, and phenanthroquinolizidine 1c, has been achieved in 46%, 49%, and 42% overall yield, respectively, starting from the corresponding phenanthrene-9-carboxaldehyde. Compound exhibited potent inhibition activity in three human cancer cell lines, with IC(50) values ranging from 104 to 130 nM. The structure-activity relations of these alkaloids and some of their synthetic intermediates against the three cell lines were also described.[Abstract] [Full Text] [Related] [New Search]