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New Cyclic Diarylheptanoids from Platycarya strobilacea.

Molecules (Basel, Switzerland)2020Ding WB, Zhao RY, Li GH, et al.
Study designOther primary literature
SubjectHuman & animal

Abstract

Five new cyclic diarylheptanoids (platycary A-E, compounds 1-5) and three previously identified analogues (i.e., phttyearynol (compound 6), myricatomentogenin (compound 7), and juglanin D (compound 8)) were isolated from the stem bark of Platycarya strobilacea. The structures of these compounds were determined using NMR, HRESIMS, and electronic circular dichroism (ECD) data. The cytotoxicity of compounds 1-5 and their ability to inhibit nitric oxide (NO) production, as well as protect against the corticosterone-induced apoptosis of Pheochromocytoma (PC12) cells, were evaluated in vitro using the appropriate bioassays. Compounds 1 and 2 significantly inhibited the corticosterone-induced apoptosis of PC12 cells at a concentration of 20 μΜ.

MeSH

AnimalsCell Line, TumorCell SurvivalDiarylheptanoidsHumansJuglandaceaeMolecular StructureNeoplasmsNitric OxidePlant ExtractsRats

DOI 10.3390/molecules25246034

PMID 33419270

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