| Literature DB >> 27966950 |
Yuben Qiao1, Qianqian Xu1, Zhengxi Hu1, Xiao-Nian Li2, Ming Xiang1, Junjun Liu1, Jinfeng Huang1, Hucheng Zhu1, Jianping Wang1, Zengwei Luo1, Yongbo Xue1, Yonghui Zhang1.
Abstract
Eighteen compounds, including eight new cassane-type furanoditerpenoids, 3β-hydroxyphanginin H (1), 3β-acetoxyphanginin H (2), 7β-acetoxyphanginin H (3), 7β-hydroxyphanginin H (4), 4-epi-3β-hydroxycaesalpinilinn (5), 4-epi-3β-acetoxycaesalpinilinn (6), 20-acetoxytaepeenin D (7), and tomocin E (8), along with 10 known compounds (9-18) were isolated from the roots of Caesalpinia decapetala. Compounds 1-13 were isolated from C. decapetala for the first time. The new compounds with their absolute configurations were determined by extensive spectroscopic analysis, single-crystal X-ray diffraction, and electronic circular dichroism calculations. Compounds 1, 4, 5, 7, and 11 exhibited inhibitory activities against the SW1990 human pancreatic cancer cell line with IC50 values ranging from 2.9 to 8.9 μM.Entities:
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Year: 2016 PMID: 27966950 DOI: 10.1021/acs.jnatprod.6b00910
Source DB: PubMed Journal: J Nat Prod ISSN: 0163-3864 Impact factor: 4.050