Journal of Fungi · 2021 · 17 citations · 25 references
PharmacyMedicinal ChemistryPharmacologyDrug DiscoveryMass Spectrometric AnalysisStructure-activity RelationshipsMetabolite IdentificationQualitative Structure-activity RelationshipsQuantitative Structure-activity RelationshipsStructure-activity Relationship AnalysisTerpenoid BiosynthesisBioactive ConstituentsCarbon Skeleton RearrangementCircular DichroismCircular Dichroism AnalysisElectronic Circular DichroismImmunosuppressive CompoundsMass Spectrometric IdentificationSingle Crystal Analysis
The aim of this work was to comprehensively understand the chemical constituents of the edible mushroom Craterellus ordoratus and their bioactivity. A chemical investigation on this mushroom led to the isolation of 23 sesquiterpenoids including eighteen previously undescribed bergamotane sesquiterpenes, craterodoratins A–R (1–18), and one new victoxinine derivative, craterodoratin S (19). The new structures were elucidated by detailed interpretation of spectrometric data, theoretical nuclear magnetic resonance (NMR) and electronic circular dichroism (ECD) calculations, and single-crystal X-ray crystallographic analysis. Compounds 1 and 2 possess a ring-rearranged carbon skeleton. Compounds 3, 10, 12–15, 19, 20 and 23 exhibit potent inhibitory activity against the lipopolysaccharide (LPS)-induced proliferation of B lymphocyte cells with the IC50 values ranging from 0.67 to 22.68 μM. Compounds 17 and 20 inhibit the concanavalin A (ConA)-induced proliferation of T lymphocyte cell with IC50 values of 31.50 and 0.98 μM, respectively. It is suggested that C. ordoratus is a good source for bergamotane sesquiterpenoids, and their immunosuppressive activity was reported for the first time. This research is conducive to the further development and utilization of C. ordoratus.
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Nobuaki Matsumori, Daisuke Kaneno, Michio Murata et al. · The Journal of Organic Chemistry · 1999 · 769 citations