Isolation and Characterization of trans‐p‐Hydroxycinnamoyl Meroterpenoids from Ganoderma sinensis

Author:

Yin Yan‐Jiao1,Zhou Hong1,Zhang Jiao‐Jiao1,Cai Dan1,Yuan Yuan‐Nan1,Yang Zhong‐Hui1,Cheng Yong‐Xian123ORCID

Affiliation:

1. Institute for Inheritance-Based Innovation of Chinese Medicine School of Pharmaceutical Sciences, Health Science Center Shenzhen University Shenzhen 518060 P. R. China

2. State Key Laboratory of Southwestern Chinese Medicine Resources Chengdu University of Traditional Chinese Medicine Chengdu 611137 P. R. China

3. Guangdong Key Laboratory for Functional Substances in Medicinal Edible Resources and Healthcare Products School of Life Sciences and Food Engineering Hanshan Normal University Chaozhou 521041 P. R. China

Abstract

AbstractZizhines V, W, Y, Z, (±)‐zizhines X, and Z1Z3, and (±)‐ganosinensol L, thirteen new compounds including four pairs of enantiomers and a known compound (−)‐ganosinensol L, were isolated from the fruiting bodies of Ganoderma sinensis. Their structures were identified by spectroscopic, computational methods, and CD (circular dichroism spectroscopy) comparisons. Zizhines V−Z and Z1Z3 are meroterpenoids consisting of the phenolic and the terpenoidal parts. All the compounds except zizhine Z3 bear a common trans‐p‐hydroxycinnamoyl group. Biological evaluation shows that (−)‐zizhine Z1 inhibits cell migration in the MDA‐MB‐231 cell lines. The present study discloses the chemical profiling of G. sinensis and paves the way for its development as functional products to benefit chronic disorders.

Funder

National Natural Science Foundation of China

National Science Fund for Distinguished Young Scholars

Shenzhen University

Publisher

Wiley

Subject

Molecular Biology,Molecular Medicine,General Chemistry,Biochemistry,General Medicine,Bioengineering

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