Simple jQuery Dropdowns
Please use this identifier to cite or link to this item:
Title: A new cytotoxic daphnane diterpenoid, rediocide G, from Trigonostemon reidioides
Authors: Atchara Tempeam
Nopporn Thasana
Chitkavee Pavaro
Wongsatit Chuakul
Pongpun Siripong
Somsak Ruchirawat
Mahidol University
The Institute of Science and Technology for Research and Development, Mahidol University
Chulabhorn Research Institute
National Cancer Institute Thailand
Keywords: Chemistry;Pharmacology, Toxicology and Pharmaceutics
Issue Date: 1-Oct-2005
Citation: Chemical and Pharmaceutical Bulletin. Vol.53, No.10 (2005), 1321-1323
Abstract: Rediocide G (7), a new daphnane diterpenoid, was isolated from the roots of Trigonostemon reidioides (Euphorbiaceae), together with two congeners, rediocide A and rediocide B, (+)-syringaresinol, scopoletin, tomentin and stigmasterol. The structure of the new natural product was elucidated by comparison of its NMR and mass spectral data with those of previously known rediocides and confirmed by extensive 2D NMR spectral analysis. Rediocide G (7) was found to be cytotoxic to various cancer cell lines. © 2005 Pharmaceutical Society of Japan.
ISSN: 13475223
Appears in Collections:Scopus 2001-2005

Files in This Item:
There are no files associated with this item.

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.