Planta Med 2012; 78(2): 160-165
DOI: 10.1055/s-0031-1280293
Natural Product Chemistry
Original Papers
© Georg Thieme Verlag KG Stuttgart · New York

Isolation of Apoptosis-Inducing Stilbenoids from Four Members of the Orchidaceae Family

Russell B. Williams1 , Steven M. Martin1 , Jin-Feng Hu1 , Eliane Garo1 , Stephanie M. Rice1 , Vanessa L. Norman1 , Julie A. Lawrence1 , Grayson W. Hough1 , Matt G. Goering1 , Mark O'Neil-Johnson1 , Gary R. Eldridge1 , Courtney M. Starks1
  • 1Lead Discovery and Rapid Structure Elucidation Group, Sequoia Sciences, Inc., St. Louis, Missouri, USA
Weitere Informationen

Publikationsverlauf

received June 6, 2011 revised Sept. 1, 2011

accepted Sept. 20, 2011

Publikationsdatum:
14. Oktober 2011 (online)

Abstract

High-throughput natural product research produced a suite of anticancer hits among several species of the Orchidaceae family (Oncidium microchilum, O. isthmi, and Myrmecophila humboldtii). A commercial Oncidium sp. was also examined as a convenient source of additional material. Isolation and structure elucidation led to the identification of fifteen stilbenoids including a new phenanthraquinone and two new dihydrostilbenes. NMR data for structure elucidation and dereplication were acquired utilizing a Bruker BioSpin TCI 1.7-mm MicroCryoProbe or a 5-µL CapNMR capillary microcoil. Several compounds inhibited proliferation of NCI-H460 and M14 cancer cell lines. All compounds were also examined for their ability to induce apoptosis. Apoptosis induction was determined by measuring caspase 3/7 activation and LDH release in a NCI-H460 cell line. Based on these results, a portion of the extract from a commercially available Oncidium sp. was chemically modified in an attempt to obtain additional phenanthraquinones.

Supporting Information

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Dr. Russell B. Williams

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