A Review of Cinnamic Acid’s Skeleton Modification: Features for Antibacterial-Agent-Guided Derivatives

Author:

Annuur Rose Malina1ORCID,Triana Desita2,Ernawati Teni1,Murai Yuta2,Aswad Muhammad3ORCID,Hashimoto Makoto2,Tachrim Zetryana Puteri1ORCID

Affiliation:

1. Research Center for Pharmaceutical Ingredient and Traditional Medicine, National Research and Innovation Agency, Kawasan Sains Teknologi (KST) BJ Habibie, Serpong, South Tangerang 15314, Indonesia

2. Division of Applied Bioscience, Graduate School of Agriculture, Hokkaido University, Kita 9, Nishi 9, Kita-ku, Sapporo 0608589, Japan

3. Faculty of Pharmacy, Hasanuddin University, Makassar 90245, Indonesia

Abstract

Antimicrobial resistance has emerged as a significant danger to global health, and the need for more effective antimicrobial resistance (AMR) control has been highlighted. Cinnamic acid is abundant in plant products and is a potential starting material for further modification, focusing on the development of new antimicrobial compounds. In the following review, we describe the classification of critical antibacterial-guided reactions applied to the main skeleton structure of cinnamic acid derivatives over the last decade. Of all of the main parts of cinnamic acids, the phenyl ring and the carboxylic group significantly affect antibacterial activity. The results presented in the following review can provide valuable insights into considerable features in the organic modification of cinnamic acids related to antibacterial medication development and the food industry.

Funder

JST SPRING

Cooperative Research Program of the Network Joint Research Center for Materials and Devices

National Research and Innovation Agency (BRIN) in collaboration with the Education Fund Management Institute

Publisher

MDPI AG

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