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首页> 外文期刊>The Journal of Organic Chemistry >Indoxamycins A-F. Cytotoxic Tricycklic Polypropionates from aMarine-Derived Actinomycete
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Indoxamycins A-F. Cytotoxic Tricycklic Polypropionates from aMarine-Derived Actinomycete

机译:吲哚霉素A-F。源自海洋的放线菌的细胞毒性三环聚丙酸酯

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摘要

Six antitumor antibiotics of a new structure class, indoxamycins A-F (1-6), were isolated from asaline culture group of marine-derived actinomyces whose strains showed approximately 96%sequence homology of 16S rDNA with the family streptomycetaceae. The structures of theseindoxamycins, which are unusual polyketides composed of six consecutive chiral centers, wereassigned by combined spectral and chemical methods. In feeding experiments using a stable isotopelabel, indoxamycin A was assembled from propionate units initially forming the aglyconpentamethyl indeno furan. The discovery of these unprecedented compounds from marine-derivedactinomycetes, a low gene homology genus, offers a significant opportunity for drug discovery.
机译:从海洋衍生的放线菌的碱性培养组中分离出六种新结构类型的抗肿瘤抗生素吲哚霉素A-F(1-6),它们的菌株显示16S rDNA与链霉菌科大约96%的序列同源性。这些indoxamycins是由六个连续的手性中心组成的不寻常的聚酮化合物,其结构通过光谱和化学方法联合确定。在使用稳定同位素标记物的饲养实验中,从最初形成无糖苷五甲基茚满呋喃的丙酸酯单元组装了吲哚霉素A。从海洋同源放线菌(一种低基因同源性属)中发现这些前所未有的化合物,为药物发现提供了重要的机会。

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