Four Pairs of Neuroprotective Aryldihydronaphthalene‐Type Lignanamide Enantiomers from the Herbs of Solanum lyratum

Author:

Mi Si‐Hui1,Chang Ye1,Zhang Xin1,Hou Jiao‐Yang1,Niu Jia‐Qi1,Hao Jin‐Le2,Yao Guo‐Dong1,Lin Bin3,Huang Xiao‐Xiao1,Bai Ming1,Song Shao‐Jiang1ORCID

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 P. R. China

2. School of Pharmaceutical Engineering Shenyang Pharmaceutical University Shenyang 110016 P. R. China

3. Wuya College of Innovation Shenyang Pharmaceutical University Shenyang 110016 P. R. China

Abstract

AbstractFour pairs of aryldihydronaphthalene‐type lignanamide enantiomers were isolated from Solanum lyratum (Solanaceae). The enantiomeric separation was accomplished by chiral‐phase HPLC, and five undescribed compounds were elucidated. Analysis by various spectroscopy and ECD calculations, the structures of undescribed compounds were illuminated. The neuroprotective effects of all compounds were evaluated using H2O2‐induced human neuroblastoma SH‐SY5Y cells and AchE inhibition activity. Among them, compound 4 a exhibited remarkable neuroprotective effects at high concentrations of 25 and 50 μmol/L comparable to Trolox. Compound 1 a showed the highest AchE inhibition with the IC50 value of 3.06±2.40 μmol/L. Molecular docking of the three active compounds was performed and the linkage between the compounds and the active site of AchE was elucidated.

Funder

Liaoning Revitalization Talents Program

Publisher

Wiley

Subject

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

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