Two New Enantiomers of Phenylethanoid and Their Anti‐Inflammatory Activities

Author:

Jia Qi1,Yang Pei‐Yuan1,Li Ya‐Ling1,Yao Guo‐Dong1,Song Shao‐Jiang1,Huang Xiao‐Xiao1ORCID

Affiliation:

1. Key Laboratory of Computational Chemistry-Based Natural Antitumor Drug Research & Development Liaoning Province Engineering Research Center of Natural Medicine Active Molecule Research & Development Liaoning Province Key Laboratory of Natural Bioactive Compounds Discovery & Modification Shenyang School of Traditional Chinese Materia Medica Shenyang Pharmaceutical University Shenyang 110016 Liaoning China

Abstract

AbstractIn this phytochemical investigation, two pairs of new phenylethanoid derivative enantiomers (1a/1b and 2a/2b), a new phenylethanoid derivative 3b, and seven known compounds (3a, 49) were isolated from the leaves of Picrasma quassioides. Spectroscopic techniques were used for the elucidation of their chemical structures, and the absolute configurations were determined by a comparison between the experimental and calculated ECD data, as well as the application of Snatzke's method. Compounds (1a/1b3a/3b) were measured for their production of NO levels in LPS‐induced BV‐2 microglial cells. The results showed that all compounds exhibited potential inhibitory effects, and compound 1a showed stronger activity than the positive control.

Funder

Liaoning Revitalization Talents Program

Shenyang Pharmaceutical University

Publisher

Wiley

Subject

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

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