Amino acid ester-coupled caffeoylquinic acid derivatives as potential hypolipidemic agents: synthesis and biological evaluation. 2021

Xi Zhang, and Dong-Yun Liu, and Hai Shang, and Yi Jia, and Xu-Dong Xu, and Yu Tian, and Peng Guo
Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences, Peking Union Medical College No. 151, Malianwa North Road, Haidian District Beijing 100193 P. R. China ytian@implad.ac.cn 18010100068@163.com.

Pandanus tectorius (L.) Parkins. (PTPs) is rich in caffeoylquinic acids and amino acids, especially some essential amino acids, such as valine, phenylalanine, and so forth. A series of novel amino acid ester-coupled caffeoylquinic acid derivatives have been designed and synthesized. Biological evaluation suggested that some amino acid ester-coupled derivatives exhibited varying degrees of lipid-lowering effects on oleic acid-elicited lipid accumulation in HepG2 liver cells. Particularly, derivatives 6c, 6d, 6e and 6f exhibited comparable potential lipid-lowering effect with the positive control simvastatin and chlorogenic acid. Further studies on the mechanism of 6c, 6d, 6e and 6f revealed that the lipid-lowering effects were related to their regulation of TG levels and mRNA levels of lipometabolic-modulating genes, and merit further investigation.

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