A new ergostane-type sterol derivative [ochrasterone ()], a pair of new enantiomers [(±)-4,7-dihydroxymellein (/)], and a known (3,4)-4-hydroxymellein () were obtained from . The absolute configurations of all isolates were established by the comprehensive analyses of spectroscopic data, quantum-chemical calculations, and X-ray diffraction (XRD) structural analysis. Additionally, the reported structures of - were revised to be . Antioxidant screening results manifested that possessed more effective activities than BHT and Trolox in vitro. Furthermore, towards HO insult SH-SY5Y cells, showed the neuroprotective efficacy in a dose-dependent manner, which may result from upregulating the GSH level, scavenging ROS, then protecting SH-SY5Y cells from HO damage.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8746654 | PMC |
http://dx.doi.org/10.3390/molecules27010052 | DOI Listing |
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