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比马霉素A至E以及比马酮:从一种陆生链霉菌中分离得到的新型醌类抗生素的结构解析及生物活性

Bhimamycin A to approximately E and bhimanone: isolation, structure elucidation and biological activity of novel quinone antibiotics from a terrestrial Streptomycete.

作者信息

Fotso Serge, Maskey Rajendra P, Grün-Wollny Iris, Schulz Klaus-Peter, Munk Morton, Laatsch Hartmut

机构信息

Department of Organic Chemistry, University of Göttingen, Tammannstrasse 2, D-37077 Göttingen, Germany.

出版信息

J Antibiot (Tokyo). 2003 Nov;56(11):931-41. doi: 10.7164/antibiotics.56.931.

Abstract

From the ethyl acetate extract of a terrestrial Streptomycete isolate, five new quinone antibiotics, bhimamycin A (2a), B (2b), C (3c), D (5a), E (7) and the new tetralone bhimanone (8) were isolated together with the known microbial products chrysophanol (1a), aloesaponarin II (1b), 3,8-dihydroxy-1-methylanthraquinone-2-carboxylic acid (1c), adenosine, 2'-deoxyadenosine, phenylacetamide, and 2-(p-hydroxyphenyl)ethanol. The structures of these natural products were deduced from the spectral data and confirmed by comparison with related compounds from the literature and by synthesis.

摘要

从一株陆生链霉菌分离物的乙酸乙酯提取物中,分离出了五种新的醌类抗生素,即比马霉素A(2a)、B(2b)、C(3c)、D(5a)、E(7)以及新的四氢萘酮比马酮(8),同时还分离出了已知的微生物产物大黄酚(1a)、芦荟皂素II(1b)、3,8 - 二羟基 - 1 - 甲基蒽醌 - 2 - 羧酸(1c)、腺苷、2'-脱氧腺苷、苯乙酰胺和2 - (对羟基苯基)乙醇。这些天然产物的结构通过光谱数据推导得出,并通过与文献中相关化合物的比较以及合成进行了确认。

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