| Literature DB >> 25699579 |
Yang Liao1, Xia Liu, Jing Yang, Yuan-Zhi Lao, Xing-Wei Yang, Xiao-Nian Li, Jing-Jing Zhang, Zhi-jie Ding, Hong-Xi Xu, Gang Xu.
Abstract
Hypersubones A and B (1, 2), two adamantane type polycyclic polyprenylated acylphloroglucinols possessing an unprecedented seco-adamantane architecture and a tetracyclo-[6.3.1.1(3,10).0(4,8)]-tridecane core combined with a peroxide ring, respectively, were isolated from Hypericum subsessile together with three analogues (3-5). Their structures were determined by extensive NMR spectroscopic analysis, ECD calculations, and single-crystal X-ray diffraction. Compound 2 exhibited significant cytotoxicities against four human cancer lines in vitro (IC50 0.07-7.52 μM).Entities:
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Year: 2015 PMID: 25699579 DOI: 10.1021/acs.orglett.5b00100
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005