Luesch H, Yoshida W Y, Moore R E, Paul V J
Department of Chemistry, University of Hawaii at Manoa, Honolulu, Hawaii 96822, USA.
J Nat Prod. 2000 Oct;63(10):1437-9. doi: 10.1021/np000104n.
An analogue of the potent microfilament-disrupter lyngbyabellin A (1) has been isolated as a minor metabolite from the marine cyanobacterium Lyngbya majuscula collected at Apra Harbor, Guam. It possesses slightly weaker cytotoxicity than 1 and has been named lyngbyabellin B (2). Primarily NMR spectroscopy was used to determine its structure. The absolute configuration of 2 has been ascertained by chiral HPLC analysis of degradation products and by comparison with lyngbyabellin A (1). The known modified tetrapeptide lyngbyapeptin A (3) has also been found in the same extract, and its absolute stereochemistry could be determined for the first time.
一种强效微丝破坏剂林比阿贝林A(1)的类似物已从关岛阿普拉港采集的海洋蓝藻大鞘丝藻中作为次要代谢产物分离出来。它的细胞毒性比1略弱,被命名为林比阿贝林B(2)。主要通过核磁共振光谱确定其结构。通过对降解产物的手性高效液相色谱分析并与林比阿贝林A(1)比较,确定了2的绝对构型。在同一提取物中还发现了已知的修饰四肽林比阿肽A(3),并首次确定了其绝对立体化学结构。