1. Academic Validation
  2. New 29-nor-cycloartanes with a 3,4-seco- and a novel 2,3-seco-structure from the leaves of Sinocalycanthus chinensis

New 29-nor-cycloartanes with a 3,4-seco- and a novel 2,3-seco-structure from the leaves of Sinocalycanthus chinensis

  • Bioorg Med Chem. 2011 May 1;19(9):2790-6. doi: 10.1016/j.bmc.2011.03.055.
Yoshiki Kashiwada 1 Kazuya Nishimura Shin-ichiro Kurimoto Yoshihisa Takaishi
Affiliations

Affiliation

  • 1 Graduate School of Pharmaceutical Sciences, University of Tokushima, 1-78 Shomachi, Tokushima 770-8505, Japan. kasiwada@ph.tokushima-u.ac.jp
Abstract

Eight new triterpenoids, including sinocalycanchinensins A-E (1-5) with a 3,4-seco-29-nor-cycloartane skeleton, sinocalycanchinensin F (6) possessing a novel 2,3-seco-29-nor-cycloartane skeleton, and 29-nor-cycloartanes, sinocalycanchinensins G and H (7 and 8), have been isolated from the leaves of Sinocalycanthus chinensis. Their structures were elucidated on the basis of spectroscopic examinations. The cytotoxicities of the isolated new Triterpenes against a panel of human Cancer cell lines, including multi-drug resistant (MDR) Cancer cell lines, were also evaluated. Compound 5 demonstrated enhanced cytotoxicity against MDR KB cells in the presence of colchicine, although all the compounds showed moderate or no cytotoxicities.

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