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  2. Design, Synthesis, and In Vitro and In Vivo Biological Evaluation of Limonin Derivatives for Anti-Inflammation Therapy

Design, Synthesis, and In Vitro and In Vivo Biological Evaluation of Limonin Derivatives for Anti-Inflammation Therapy

  • J Agric Food Chem. 2021 Nov 17;69(45):13487-13499. doi: 10.1021/acs.jafc.1c04989.
Ming Bian 1 2 3 Guohua Gong 1 3 4 Pang Lei 5 Huanhuan Du 1 3 Chunmei Bai 1 3 Chengxi Wei 1 3 Zheshan Quan 2 Qianqian Ma 1 3
Affiliations

Affiliations

  • 1 Inner Mongolia Key Laboratory of Mongolian Medicine Pharmacology for Cardio-Cerebral Vascular System, Inner Mongolia, Tongliao 028000, P. R. China.
  • 2 College of Pharmacy, Yanbian University, Yanji City, Jilin 133002, China.
  • 3 Institute of Pharmaceutical Chemistry and Pharmacology, Inner Mongolia Minzu University, Inner Mongolia Autonomous Region, Tongliao 028000, China.
  • 4 First Clinical Medical of Inner Mongolia Minzu University, Inner Mongolia, Tongliao 028000, P. R. China.
  • 5 Nanchong Key Laboratory of Individualized Drug Therapy, Department of Pharmacy, the Second Clinical Medical College of North Sichuan Medical College, Nanchong Central Hospital, Nanchong, Sichuan 637000, China.
Abstract

In this study, limonin derivatives were used to design new anti-inflammatory compounds with high pharmacological activity and low toxicity. A total of 23 new limonin derivatives were discovered, synthesized, and screened for their anti-inflammatory activity against lipopolysaccharide (LPS)-treated RAW 264.7 cells. Of them, compound f4 was found to be the most active, with a higher efficiency compared with limonin and celecoxib. Subsequently, we studied the mechanism underlying the activity of f4 and found that it inhibited proinflammatory cytokines by blocking the NF-κB/MAPK signaling pathway in LPS-treated RAW 264.7 cells as well as mice. In conclusion, f4 may be a promising anti-inflammatory lead compound.

Keywords

RAW 264.7 cells; acute lung injury; anti-inflammatory; limonin; structural modification.

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