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阿塔克霉素 A-C,由链霉菌 C38 产生的具有 22 个成员的抗肿瘤大环内酯。

Atacamycins A-C, 22-membered antitumor macrolactones produced by Streptomyces sp. C38.

机构信息

Institut für Chemie, Technische Universität Berlin, Berlin, Germany.

出版信息

J Antibiot (Tokyo). 2011 Dec;64(12):775-80. doi: 10.1038/ja.2011.96. Epub 2011 Oct 19.

Abstract

Three new 22-membered macrolactone antibiotics, atacamycins A-C, were produced by Streptomyces sp. C38, a strain isolated from a hyper-arid soil collected from the Atacama Desert in the north of Chile. The metabolites were discovered in our HPLC-diode array screening and isolated from the mycelium by extraction and chromatographic purification steps. The structures were determined by mass spectrometry and NMR experiments. Atacamycins A, B and C exhibited moderate inhibitory activities against the enzyme phosphodiesterase (PDE-4B2), whereas atacamycin A showed a moderate antiproliferative activity against adeno carcinoma and breast carcinoma cells.

摘要

三种新的 22 元大环内酯抗生素,atacamycins A-C,由从智利北部阿塔卡马沙漠采集的极端干旱土壤中分离出的链霉菌 C38 产生。这些代谢产物是通过我们的 HPLC-二极管阵列筛选发现的,并通过提取和色谱纯化步骤从菌丝体中分离出来。结构通过质谱和 NMR 实验确定。Atacamycins A、B 和 C 对酶磷酸二酯酶(PDE-4B2)表现出中等抑制活性,而 atacamycin A 对腺癌和乳腺癌细胞表现出中等的抗增殖活性。

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