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马里隆内 A-C,来源于海绵真菌穗枝犁头霉的香豆素

Marilones A-C, phthalides from the sponge-derived fungus Stachylidium sp.

机构信息

Institute for Pharmaceutical Biology, University of Bonn, Nussallee 6, D-53115 Bonn, Germany.

出版信息

Beilstein J Org Chem. 2011;7:1636-42. doi: 10.3762/bjoc.7.192. Epub 2011 Dec 5.

Abstract

The marine-derived fungus Stachylidium sp. was isolated from the sponge Callyspongia sp. cf. C. flammea. Culture on a biomalt medium supplemented with sea salt led to the isolation of three new phthalide derivatives, i.e., marilones A-C (1-3), and the known compound silvaticol (4). The skeleton of marilones A and B is most unusual, and its biosynthesis is suggested to require unique biochemical reactions considering fungal secondary metabolism. Marilone A (1) was found to have antiplasmodial activity against Plasmodium berghei liver stages with an IC(50) of 12.1 µM. Marilone B (2) showed selective antagonistic activity towards the serotonin receptor 5-HT(2B) with a K(i) value of 7.7 µM.

摘要

海洋来源的真菌 Stachylidium sp. 是从海绵 Callyspongia sp. cf. C. flammea 中分离得到的。在添加海水盐的生物麦芽培养基上培养导致了三个新的邻苯二甲酸衍生物的分离,即 marilones A-C(1-3)和已知化合物 silvaticol(4)。Marilones A 和 B 的骨架非常不寻常,考虑到真菌的次生代谢,其生物合成被认为需要独特的生化反应。Marilone A(1)被发现对 Plasmodium berghei 肝期具有抗疟原虫活性,IC(50)为 12.1 µM。Marilone B(2)对 5-羟色胺受体 5-HT(2B)表现出选择性拮抗活性,K(i)值为 7.7 µM。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79cc/3252867/a823531bb4a8/Beilstein_J_Org_Chem-07-1636-g002.jpg

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