Five new guanacastane-type diterpenes,named guanacastepenes P–T(1–5),were isolated from cultures of the fungus Psathyrella candolleana.Their structures were elucidated on the basis of extensive spectroscopic methods...Five new guanacastane-type diterpenes,named guanacastepenes P–T(1–5),were isolated from cultures of the fungus Psathyrella candolleana.Their structures were elucidated on the basis of extensive spectroscopic methods.All of the compounds were tested for their 11b-hydroxysteroid dehydrogenase(11b-HSD1)inhibitory activity.Compound 3 exhibited inhibitory activity against both human and mouse isozymes of 11b-HSD1 with IC50 values of 6.2 and 13.9 lM,respectively.展开更多
Five previously undescribed guanacastane diterpenoids,namely psathyrellins A-E(1-5),were obtained from cultures of the mushroom Psathyrella candolleana.Their structures with absolute configurations were elucidated by ...Five previously undescribed guanacastane diterpenoids,namely psathyrellins A-E(1-5),were obtained from cultures of the mushroom Psathyrella candolleana.Their structures with absolute configurations were elucidated by extensive spectroscopic methods.Compounds 1-3 showed antibacterial activity against four strains with MIC values in a range of 16-128μg/mL.展开更多
基金the National Natural Sciences Foundation of China(U1132607,81373289).
文摘Five new guanacastane-type diterpenes,named guanacastepenes P–T(1–5),were isolated from cultures of the fungus Psathyrella candolleana.Their structures were elucidated on the basis of extensive spectroscopic methods.All of the compounds were tested for their 11b-hydroxysteroid dehydrogenase(11b-HSD1)inhibitory activity.Compound 3 exhibited inhibitory activity against both human and mouse isozymes of 11b-HSD1 with IC50 values of 6.2 and 13.9 lM,respectively.
基金the National Key Research and Development Program of China(Grant No.2017YFC1704007).
文摘Five previously undescribed guanacastane diterpenoids,namely psathyrellins A-E(1-5),were obtained from cultures of the mushroom Psathyrella candolleana.Their structures with absolute configurations were elucidated by extensive spectroscopic methods.Compounds 1-3 showed antibacterial activity against four strains with MIC values in a range of 16-128μg/mL.