| Literature DB >> 16271376 |
Dong-Hui He1, Katsuyoshi Matsunami, Hideaki Otsuka, Takakazu Shinzato, Mitsunori Aramoto, Masahiko Bando, Yoshio Takeda.
Abstract
Eight ent-kaurane glucosides, named tricalysiosides H-O, were isolated from Tricalysia dubia. Tricalysioside H possessed a hydroxyl group at the 1-position, to which the glucose moiety was attached. The structure was first elucidated by means of spectroscopic data analysis and finally confirmed by X-ray crystallography. Since acid hydrolysis of 1 gave D-glucose, the aglycone was proved to have an enantio-kaurane type skeleton. The structures of tricalysiosides I-O were mainly elucidated from analysis of spectroscopic evidence.Entities:
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Year: 2005 PMID: 16271376 DOI: 10.1016/j.phytochem.2005.09.014
Source DB: PubMed Journal: Phytochemistry ISSN: 0031-9422 Impact factor: 4.072