| Literature DB >> 19467682 |
Yoshihito Shiono1, Sadayoshi Motoki, Takuya Koseki, Tetsuya Murayama, Masato Tojima, Ken-ichi Kimura.
Abstract
The methanol extract of fruiting bodies of the ascomycete Xylaria polymorpha afforded three isopimarane diterpene glycosides, namely, 16-alpha-D-mannopyranosyloxyisopimar-7-en-19-oic acid (1), 15-hydroxy-16-alpha-D-mannopyranosyloxyisopimar-7-en-19-oic acid (2), and 16-alpha-D-glucopyranosyloxyisopimar-7-en-19-oic acid (3). Their structures were determined by spectroscopic methods and by single-crystal X-ray analysis. They showed cytotoxicity against human cancer cell lines and exhibited IC50 values ranging from 71 to 607 microM. Further studies on the cytotoxicity of these compounds against HL60 cells demonstrated that they induced apoptosis along with typical DNA fragmentation. It was observed that 2 was less active than 1 and 3.Entities:
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Year: 2009 PMID: 19467682 DOI: 10.1016/j.phytochem.2009.03.023
Source DB: PubMed Journal: Phytochemistry ISSN: 0031-9422 Impact factor: 4.072