Zhang Shuaibing, Huang Ying, He Shijun, Chen Heping, Li Zhenghui, Wu Bin, Zuo Jianping, Feng Tao, Liu Jikai
School of Pharmaceutical Sciences, South-Central University for Nationalities Wuhan 430074 China
Leibniz Research Group - Biobricks of Microbial Natural Product Syntheses, Leibniz Institute for Natural Product Research and Infection Biology (HKI) Adolf-Reichwein-Str. 23 07745 Jena Germany.
RSC Adv. 2018 Jul 2;8(42):23914-23918. doi: 10.1039/c8ra04226h. eCollection 2018 Jun 27.
A chemical study of the common species present in Yunnan province, southwest China led to the identification of a pair of epimers named albatredines A (1) and B (2). They feature a natural unprecedented 1,2,4-oxadiazolidin-5-one skeleton. The acyl substitution pattern and complete configurational assignments were deduced from the comparison between experimental and theoretical C NMR and ECD data, respectively. Bioassay results showed that compound 1 exhibited a weak immunosuppressive activity against the concanavalin A-induced T lymphocyte cell proliferation (IC 2.99 μM).
对中国西南部云南省常见物种进行的化学研究,鉴定出了一对差向异构体,命名为阿尔巴曲定A(1)和B(2)。它们具有一种天然的前所未有的1,2,4-恶二唑烷-5-酮骨架。分别通过实验和理论碳核磁共振(C NMR)及电子圆二色光谱(ECD)数据的比较,推导了酰基取代模式和完整的构型归属。生物活性测试结果表明,化合物1对刀豆蛋白A诱导的T淋巴细胞增殖表现出微弱的免疫抑制活性(半数抑制浓度IC为2.99 μM)。