Affiliation:
1. College of Pharmacy Dankook University 119 Dandae-ro Dongnam-gu Cheonan Korea
2. College of Pharmacy Woosuk University 443 Samnye-ro Wanju-gun Jeonbuk Korea
Abstract
AbstractHerein, we describe the synthesis of the proposed structure of the caffeamide alkaloid bassiamide A. The amide moiety of bassiamide A was readily formed via an amide coupling reaction between caffeic acid and the known N‐(3‐aminopropyl)‐3‐methylbutanamide. However, the spectral data of the synthesized bassiamide A did not agree with that of a previous study. The structure of the synthesized bassiamide A was confirmed using combined two‐dimensional NMR analysis. Extended analyses of the bioactivity of the synthesized bassiamide A revealed its efficacy in protecting dopaminergic neurons from MPP+‐induced neurotoxicity in Caenorhabditis elegans. Additionally, treatment with bassiamide A notably ameliorated the impaired food‐sensing ability and locomotion of Caenorhabditis elegans, suggesting a protective effect on the functionality of dopaminergic neurons.