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抗结核剂 diaportheone B: 其类似物的合成、绝对构型确定及抗结核活性。

Antituberculosis agent diaportheone B: synthesis, absolute configuration assignment, and anti-TB activity of its analogues.

机构信息

Division of Organic Chemistry, CSIR-National Chemical Laboratory, Dr. Homi Bhabha Road, Pune, 411008, India.

出版信息

Org Biomol Chem. 2012 Jul 28;10(28):5385-94. doi: 10.1039/c2ob25831e. Epub 2012 May 25.

Abstract

First synthesis of diaportheone B, an antituberculosis agent isolated from endophytic fungus Diaporthe sp. P133 is reported using two complementary routes, a one step and a three-step sequence. The absolute configuration of diaportheone B was determined by using X-ray crystal structure analysis of its dibromo derivative. In addition, we have prepared several close analogues of diaportheone B and determined their anti-TB potential using Alamar-blue assay (H(37)Rv).

摘要

首次报道了从内生真菌 Diaporthe sp. P133 中分离得到的抗结核药物二盘菌素 B 的全合成。该化合物的合成都采用了两种互补的方法,一种是一步法,另一种是三步法。通过其二溴代衍生物的 X 射线晶体结构分析确定了二盘菌素 B 的绝对构型。此外,我们还制备了几种二盘菌素 B 的类似物,并通过 Alamar-blue assay (H(37)Rv) 测定了它们的抗结核活性。

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