Chen Xuan-Qin, Li Yan, Li Kun-Zhi, Peng Li-Yan, He Juan, Wang Kou, Pan Zheng-Hong, Cheng Xiao, Li Ming-Ming, Zhao Qin-Shi, Xu Gang
State Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, Chinese Academy of Sciences, Kumning, Yunnan, People's Republic of China.
Chem Pharm Bull (Tokyo). 2011;59(10):1250-3. doi: 10.1248/cpb.59.1250.
Four new acylphloroglucinols with an unusual 6/6/5 spirocyclic skeleton, hyperbeanols A-D (1-4), were isolated from the methanol extract of Hypericum beanii along with 16 known compounds. Their structures were established on the basis of spectroscopic and X-ray diffraction analysis. Hyperbeanols A-C were three stereoisomers different only at the relative configuration of C-4 and C-13, which were distinguished by the nuclear Overhauser effect spectroscopy (NOESY) spectroscopic data in combination with the single X-ray analysis of hyperbeanol A (1). The cytotoxic activity of hyperbeanols A-D against the cancer cell lines SK-BR-3, HL-60, SMMC-7721, PANC-1, MCF-7, and K562 was also evaluated.
从赶山鞭的甲醇提取物中分离出四种具有不寻常的6/6/5螺环骨架的新酰基间苯三酚,即赶山鞭醇A-D(1-4),以及16种已知化合物。它们的结构通过光谱和X射线衍射分析确定。赶山鞭醇A-C是仅在C-4和C-13的相对构型上不同的三种立体异构体,通过核Overhauser效应光谱(NOESY)光谱数据结合赶山鞭醇A(1)的单晶X射线分析来区分。还评估了赶山鞭醇A-D对癌细胞系SK-BR-3、HL-60、SMMC-7721、PANC-1、MCF-7和K562的细胞毒性活性。