Natural Products Research Institute, College of Pharmacy, Seoul National University , San 56-1, Sillim, Gwanak, Seoul 151-742, Korea.
J Nat Prod. 2012 Dec 28;75(12):2055-61. doi: 10.1021/np3005562. Epub 2012 Nov 12.
Nine new compounds, tris-aromatic furanones (1, 2, 3a, 3b, and 4) and related bis-aromatic diesters (5a, 5b, 6a, and 6b), are described from the ascidian Synoicum sp. collected off the coast of Chuja-do, Korea. The structures of these compounds, designated as cadiolides E and G-I (1-4) and synoilides A and B (5 and 6), were determined by extensive spectroscopic analyses. The absolute configuration at the asymmetric center of cadiolide G (2) was assigned by ECD analysis. Of these new compounds, cadiolide I and the synoilides possess unprecedented carbon skeletons. Several of these compounds exhibited significant inhibition against diverse bacterial strains as well as moderate inhibition against the enzymes sortase A, isocitrate lyase, and Na(+)/K(+)-ATPase.
从韩国楚加道海域采集的海鞘 Synoicum sp. 中分离得到了 9 种新化合物,包括三芳基呋喃酮(1、2、3a、3b 和 4)和相关的双芳基二酯(5a、5b、6a 和 6b)。这些化合物被命名为 cadiolides E 和 G-I(1-4)和 synoilides A 和 B(5 和 6),其结构通过广泛的光谱分析确定。通过 ECD 分析确定了 cadiolide G(2)中不对称中心的绝对构型。在这些新化合物中,cadiolide I 和 synoilides 具有前所未有的碳骨架。其中一些化合物对多种细菌菌株表现出显著的抑制作用,对 sortase A、异柠檬酸裂解酶和 Na(+)/K(+)-ATPase 也有中等抑制作用。