Journal of Natural Products · 2020 · 15 citations · 13 references
Life SciencesBiochemistryMicrobiologyDrug DiscoveryMicrobial EcologyMycologyFungal Natural Product BiosynthesisFungal Secondary MetabolitesRetrosynthetic AnalysisTerpenoid BiosynthesisEquivalent Circulating DensityFungal Terpenoid BiosynthesisFused Ring ModificationSesquiterpene BiosynthesisTerpene CompoundsTerpenoid Glycosides
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.
13
Acute hepatic allograft rejection: Incidence, risk factors, and impact on outcome †
Russell H. Wiesner, Jake Demetris, Steven H. Belle et al. · Hepatology · 1998 · 498 citations
Life Sciences, Immunology, Surgery +17