Issue 11, 2021, Issue in Progress

Vlasoulides A and B, a pair of neuroprotective C32 dimeric sesquiterpenes with a hexacyclic 5/7/5/5/(5)/7 carbon skeleton from the roots of Vladimiria souliei

Abstract

Vlasoulides A and B (1 and 2), a pair of epimeric C32 sesquiterpene lactone dimers, featuring a 5/7/5/5/(5)/7 ring system were isolated from the roots of Vladimiria souliei. Their chemical structures were determined by comprehensive analysis of spectroscopic data, including HRESIMS and 1D and 2D NMR spectroscopic data. Their absolute configurations were established by Mosher's method and ECD experiments. Furthermore, biological studies showed that compound 1 showed prominent neuroprotective effects against glutamate-induced neurotoxicity in PC-12 cells, with EC50 values of 13.54 ± 0.33 μM, while, the EC50 value of compound 2 is greater than 30 μM.

Graphical abstract: Vlasoulides A and B, a pair of neuroprotective C32 dimeric sesquiterpenes with a hexacyclic 5/7/5/5/(5)/7 carbon skeleton from the roots of Vladimiria souliei

Supplementary files

Article information

Article type
Paper
Submitted
05 Jan 2021
Accepted
28 Jan 2021
First published
03 Feb 2021
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2021,11, 6159-6162

Vlasoulides A and B, a pair of neuroprotective C32 dimeric sesquiterpenes with a hexacyclic 5/7/5/5/(5)/7 carbon skeleton from the roots of Vladimiria souliei

Z. Wu, Q. Wang, L. Fu, R. Su, Z. Sun and H. Li, RSC Adv., 2021, 11, 6159 DOI: 10.1039/D1RA00075F

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