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Conosiligins A–D, Ring-Rearranged Tremulane Sesquiterpenoids from <i>Conocybe siliginea</i>

Juan He, Chao-Jun Pu, Meng Wang, Zheng-Hui Li, Tao Feng, Dake Zhao, Ji‐Kai Liu

2020Journal of Natural Products15 citationsDOI

Abstract

Conosiligins A–D (1–4), four ring-rearranged sesquiterpenoids, were isolated from cultures of the basidiomycete Conocybe siliginea. Their structures and absolute configurations were determined by detailed spectroscopic analyses and equivalent circulating density (ECD) calculations. Compounds 1 and 2 possess a 5/8-fused ring system, while 3 has a 5/6-fused backbone conjugated with a γ-lactone. Compound 4 is a 5,6-seco tremulane derivative with the loss of a skeletal carbon, featuring a tetracyclic system involving a pyranone moiety. Compounds 3 and 4 inhibited Con A-induced T cell proliferation with IC50 values of 12.3 and 6.6 μM, respectively.

Topics & Concepts

StereochemistryRing (chemistry)DiterpeneSesquiterpeneChemistryOrganic chemistryPhytochemistry and Biological ActivitiesNatural product bioactivities and synthesisSesquiterpenes and Asteraceae Studies
Conosiligins A–D, Ring-Rearranged Tremulane Sesquiterpenoids from <i>Conocybe siliginea</i> | Litcius