4.5 Article

Cytotoxic anthracycline and antibacterial tirandamycin analogues from a marine-derived Streptomyces sp. SCSIO 41399

期刊

JOURNAL OF ANTIBIOTICS
卷 72, 期 1, 页码 45-49

出版社

JAPAN ANTIBIOTICS RESEARCH ASSOC
DOI: 10.1038/s41429-018-0103-6

关键词

-

资金

  1. National Natural Science Foundation of China [41776169, 41476135, 21502204, 21772210, 81741154, 81741158]
  2. Science and Technology Project of Guangdong Province [2016A020222010]
  3. Pearl River S&T Nova Program of Guangzhou [201710010136]
  4. High Education Teaching and reform Research Fund Program of Hainan province [Hnjg2017ZD-3]

向作者/读者索取更多资源

Aranciamycin K (1) and isotirandamycin B (2) were isolated from a marine-derived Streptomyces sp. SCSIO 41399, along with the previously reported four anthracycline derivatives (3-6), and two known tirandamycin derivatives (7 and 8). Their structures including absolute configurations were determined by extensive analysis of their spectroscopic analysis and ECD calculation method. Most of the isolated compounds were tested for their cytotoxic, antibacterial, and antifungal activities. Compounds 2, 7 and 8 displayed potent bacteriostatic effects against Streptococcus agalactiae with MIC values of 11.5, 5.9 and 5.7 mu M, respectively. Besides, compounds 3, 5 and 6 exhibited moderate in vitro cytotoxic activities against the K562 cell lines with IC(50 )values of 22.0 +/- 0.20, 1.80 +/- 0.01 and 12.1 +/- 0.07 mu M, respectively.

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。

评论

主要评分

4.5
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据