Ahmed Atallah F, Su Jui-Hsin, Shiue Ru-Ting, Pan Xin-Jie, Dai Chang-Feng, Kuo Yao-Haur, Sheu Jyh-Horng
Department of Marine Resources, National Sun Yat-Sen University, Kaohsiung 804, Taiwan, Republic of China.
J Nat Prod. 2004 Apr;67(4):592-7. doi: 10.1021/np030286w.
Two new norsesquiterpenoids, nanonorcaryophyllenes A (1) and B (2), two new diterpenoids, nanolobatins A (3) and B (4), and a novel norditerpenoid, nanolobatin C (5), were isolated from the n-hexane extract of the Taiwanese soft coral Sinularia nanolobata. Also, two new furanone derivatives, 6 and 7, were isolated for the first time from natural sources. The structures of 1-5 were elucidated on the basis of extensive spectroscopic analyses and by comparison of the spectral data with those of the related metabolites. Nanonorcaryophyllenes A (1) and B (2) were characterized as 13-norcaryophyllenes that lack a methyl group at C-11, while nanolobatin C (5) represents the first example of a xeniaphyllane-based 17-norditerpenoid. The cytotoxicity of 1-6 against the growth of a limited panel of cancer cell lines is also described.
从台湾软珊瑚细枝软珊瑚(Sinularia nanolobata)的正己烷提取物中分离出两种新的去甲倍半萜类化合物,即细枝去甲石竹烯A(1)和B(2),两种新的二萜类化合物,即细枝叶甲素A(3)和B(4),以及一种新型的去甲二萜类化合物,细枝叶甲素C(5)。此外,还首次从天然来源中分离出两种新的呋喃酮衍生物,6和7。通过广泛的光谱分析,并将光谱数据与相关代谢物的数据进行比较,阐明了1-5的结构。细枝去甲石竹烯A(1)和B(2)被鉴定为在C-11位缺少一个甲基的13-去甲石竹烯,而细枝叶甲素C(5)代表了基于异叶叶烷的17-去甲二萜类化合物的首个实例。还描述了1-6对一组有限的癌细胞系生长的细胞毒性。