期刊
ORGANIC & BIOMOLECULAR CHEMISTRY
卷 21, 期 8, 页码 1737-1743出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/d2ob02247h
关键词
-
Three novel actinomycins, actimomycin S (1), neo-actinomycins C and D (2 and 3), and one new benzo[d]oxazole alkaloid (4) were isolated from the Streptomyces sp. strain S22. The structures of the new products were determined by spectroscopic methods, and the absolute configuration of amino acid residues was determined by Marfey's analysis. Actinomycins 1-3 exhibited antimicrobial activity against multiple resistant ESKAPE pathogens and showed potent cytotoxic activities against the HepG2 liver carcinoma cell line.
Three novel actinomycins, actimomycin S (1), neo-actinomycins C and D (2 and 3), and one new benzo[d]oxazole alkaloid (4) were isolated from the Streptomyces sp. strain S22, along with three known congeners F-9 (5), X-2 (6) and X-0 beta (7) and 2-acetylamino-3-hydroxyl-4-methyl-benzoic acid methyl ester (8). The structures of the new products were elucidated by spectroscopic methods, and the absolute configuration of amino acid residues was determined by Marfey's analysis. Actinomycin S contains an aspartic acid (Asp) residue in the beta-peptidolactone ring. This is the first report of an Asp residue within an actinomycin-type natural product. Notably, neo-actinomycins C and D feature a rare tetracyclic 5H-oxazolo[4,5-b]phenoxazine chromophore. Among these, neo-actinomycin D, with an unprecedented molecular formula, represents the highest molecular weight member in the actinomycin family. Actinomycins 1-3 exhibited antimicrobial activity against multiple resistant ESKAPE pathogens with MIC values ranging from 1.25 to 80.0 mu g mL(-1). In addition, 1-3 showed potent cytotoxic activities against the HepG2 liver carcinoma cell line with IC50 values of 0.10, 0.32, and 0.024 mu M, respectively. Furthermore, 1 inhibited cell proliferation by inducing G0-G1 phase arrest in the cell cycle.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据