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一种新型三环多酮及其生物合成前体来自内生真菌 Dothideomycete sp 的氮杂菲酮衍生物。

A novel tricyclic polyketide and its biosynthetic precursor azaphilone derivatives from the endophytic fungus Dothideomycete sp.

机构信息

Chulabhorn Graduate Institute, Chemical Biology Program, Laksi, Bangkok, Thailand.

出版信息

Org Biomol Chem. 2012 Sep 21;10(35):7220-6. doi: 10.1039/c2ob25959a. Epub 2012 Jul 30.

DOI:10.1039/c2ob25959a
PMID:22847560
Abstract

Azaphilone derivatives 1 and 2 and a novel tricyclic polyketide 3, together with a known azaphilone, austdiol (4), were isolated from the endophytic fungus Dothideomycete sp., which was isolated from a Thai medicinal plant, Tiliacora triandra. Compound 3 is the first polyketide having a tricyclic 6,6,6 ring system, which is similar to that of a terpenoid skeleton. The absolute configurations of stereogenic centers in 1-3 were addressed by Mosher's method and biosynthetic analogy with a known azaphilone isolated from the same fungus. Cytotoxic and antimicrobial activities of the isolated compounds were evaluated.

摘要

从泰国药用植物三叶芫花(Tiliacora triandra)内生真菌枝孢属(Dothideomycete sp.)中分离得到的化合物 1 和 2 是吖啶酮衍生物,3 是新型三环多酮,此外还有一个已知的吖啶酮 austdiol(4)。化合物 3 是第一个具有三环 6,6,6 环系统的多酮,类似于萜烯骨架。通过 Mosher 法和与从同一真菌中分离得到的已知吖啶酮的生物合成类似性,确定了 1-3 中立体中心的绝对构型。对分离得到的化合物进行了细胞毒性和抗菌活性评价。

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