Hubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation and Department of Pharmacology, School of Pharmacy, Tongji Medical College, Huazhong University of Science and Technology , Wuhan 430030, Hubei Province, People's Republic of China.
State Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, Chinese Academy of Sciences , Kunming 650204, Yunnan Province, People's Republic of China.
J Nat Prod. 2016 Dec 23;79(12):3134-3142. doi: 10.1021/acs.jnatprod.6b00910. Epub 2016 Dec 14.
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 IC values ranging from 2.9 to 8.9 μM.
从羊蹄甲属植物根部分离得到 18 种化合物,包括 8 种新的贝壳杉型呋喃二萜,3β-羟基黄杨宁 H(1)、3β-乙酰氧基黄杨宁 H(2)、7β-乙酰氧基黄杨宁 H(3)、7β-羟基黄杨宁 H(4)、4-表-3β-羟基美登木素(5)、4-表-3β-乙酰氧基美登木素(6)、20-乙酰氧基他皮宁 D(7)和托莫辛 E(8),以及 10 种已知化合物(9-18)。化合物 1-13 首次从羊蹄甲属植物中分离得到。通过广泛的光谱分析、单晶 X 射线衍射和电子圆二色性计算确定了新化合物的绝对构型。化合物 1、4、5、7 和 11 对 SW1990 人胰腺癌细胞系表现出抑制活性,IC 值范围为 2.9 至 8.9 μM。