| Literature DB >> 28151673 |
Chang-Shan Niu1, Yong Li1, Yun-Bao Liu1, Shuang-Gang Ma1, Fei Liu1, Li Li1, Song Xu1, Xiao-Jing Wang1, Ru-Bing Wang1, Jing Qu1, Shi-Shan Yu1.
Abstract
Pierisketolide A (1) and pierisketones B and C (2 and 3), three diterpenes with an unusual A-homo-B-nor-ent-kaurane carbon skeleton, were isolated from the roots of Pieris formosa. Their structures were characterized by a series of spectroscopic methods, X-ray diffraction, and electronic circular dichroism (ECD). Pierisketolide A (1) exhibited an analgesic effect with a 45% writhe inhibition rate at a dose of 10.0 mg/kg. The plausible biosynthetic pathways of 1-3 are proposed.Entities:
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Year: 2017 PMID: 28151673 DOI: 10.1021/acs.orglett.7b00048
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005