Key Laboratory of Marine Drugs, Chinese Ministry of Education, School of Medicine and Pharmacy, Ocean University of China, Qingdao 266003, People's Republic of China.
J Nat Prod. 2013 Apr 26;76(4):600-6. doi: 10.1021/np300771p. Epub 2013 Mar 25.
Five new polyketides, plakortoxides A (1) and B (2), simplextones C (3) and D (4), and plakorsin D (5), together with six known analogues (6-11) were isolated from the South China Sea sponge Plakortis simplex. Their structures were identified by spectroscopic and chemical methods, including NMR, MS, and IR. Experimental and calculated ECD spectra and the modified Mosher's method were used to determine the absolute configurations. Structurally, both plakortoxides A and B feature a butenolide coupled to an epoxide moiety, while simplextones C and D consist of γ-butyrolactone and cyclopentane moieties, and plakorsin D is a furan acetic acid polyketide. The cytotoxic activities of the isolates were tested, and compounds 8, 10, and 11 showed potent cytotoxicity against both K562 and HeLa tumor cell lines with IC50 values ranging from 0.8 to 5.3 μM. Compound 3 showed significant inhibitory activity against c-Met kinase.
从南海海绵 Plakortis simplex 中分离得到了五个新的聚酮化合物,分别为 plakortoxides A(1)和 B(2)、simplextones C(3)和 D(4)以及 plakorsin D(5),以及六个已知类似物(6-11)。通过光谱和化学方法,包括 NMR、MS 和 IR,确定了它们的结构。实验和计算的 ECD 光谱以及改良的 Mosher 法用于确定绝对构型。结构上,plakortoxides A 和 B 均具有与环氧化物部分偶联的丁烯内酯,而 simplextones C 和 D 由γ-丁内酯和环戊烷部分组成,plakorsin D 是一种呋喃乙酸聚酮化合物。对分离得到的化合物进行了细胞毒性测试,化合物 8、10 和 11 对 K562 和 HeLa 肿瘤细胞系表现出较强的细胞毒性,IC50 值范围为 0.8 至 5.3 μM。化合物 3 对 c-Met 激酶表现出显著的抑制活性。