Natural Product Research ( IF 2.2 ) Pub Date : 2020-12-30 , DOI: 10.1080/14786419.2020.1867131 Siqiang Chen 1, 2 , Qingbo Zhang 1, 3 , Xinya Zhang 1, 2 , Xiaodong Jiang 1, 2 , Haibo Zhang 1, 3 , Yiguang Zhu 1, 2, 3 , Changsheng Zhang 1, 2, 3 , Liping Zhang 1, 3
Abstract
A new cyclo-heptadepsipeptide xanthostatin B (1), together with isobutyryl hexapeptide (2), xanthostatin (3), TXS-1 (4) and TXS-2 (5), were isolated from the marine sponge derived Streptomyces sp. SCSIO 40064. The structures were elucidated by comprehensive spectroscopic data analyses and comparison with the literatures. The D-Val unit in 1 was assigned by Marfey’s method. The absolute configuration of 4 was determined by X-ray crystallographic analysis. Compounds 1‒5 were evaluated for the inhibitory activities against four pharmaceutical targets and six antibacterial indicator strains. Compound 5 displayed α-glucosidase inhibitory activity with IC50 value of 18.67 ± 1.27 µM.
中文翻译:
一种来自海绵相关放线菌的新黄体素类似物 Streptomyces sp。SCSIO 40064
摘要
从海绵衍生的链霉菌中分离出一种新的环七肽黄素 B ( 1 ),以及异丁酰六肽 ( 2 )、黄素 ( 3 )、TXS-1 ( 4 ) 和 TXS-2 ( 5 ) 。SCIO 40064。通过全面的光谱数据分析和与文献的比较,阐明了结构。1中的 D-Val 单位由 Marfey 方法指定。4的绝对构型由X射线晶体学分析确定。化合物1 - 5对四种药物靶点和六种抗菌指示菌株的抑制活性进行了评估。化合物5显示出α-葡萄糖苷酶抑制活性,IC 50值为18.67 ± 1.27 µM。