Charan Romila D, McKee Tawnya C, Boyd Michael R
Molecular Targets Drug Discovery Program, Center for Cancer Research, National Cancer Institute, Frederick, Maryland 21702-1201, USA.
J Nat Prod. 2002 Apr;65(4):492-5. doi: 10.1021/np010439k.
Extracts of the marine sponge Thorectandra sp. have been found to contain three new sesterterpenes, thorectandrols C (4), D (5), and E (6), together with the known compounds luffarin R (7), luffarin V (8), and palauolide (9). The structures were determined by extensive NMR spectral data analysis. Their relative stereochemistry was defined using NOE correlations and coupling constants, while CD data were used to suggest their absolute stereochemistry. Cytotoxicity data for compounds 4-9 as well as the previously reported compounds thorectandrols A and B and palauolol (1-3) against six or more human tumor cell lines are also reported.
已发现海洋海绵Thorectandra sp.的提取物含有三种新的倍半萜烯,即thorectandrols C(4)、D(5)和E(6),以及已知化合物luffarin R(7)、luffarin V(8)和帕劳内酯(9)。通过广泛的核磁共振光谱数据分析确定了它们的结构。利用核Overhauser效应(NOE)相关和耦合常数确定了它们的相对立体化学,同时利用圆二色(CD)数据推测了它们的绝对立体化学。还报道了化合物4 - 9以及先前报道的化合物thorectandrols A和B以及帕劳洛尔(1 - 3)对六种或更多种人类肿瘤细胞系的细胞毒性数据。