1. Academic Validation
  2. Synthesis and structure-activity relationship of 5-substituent-2(1H)-pyridone derivatives as anti-fibrosis agents

Synthesis and structure-activity relationship of 5-substituent-2(1H)-pyridone derivatives as anti-fibrosis agents

  • Bioorg Med Chem Lett. 2012 Mar 15;22(6):2300-2. doi: 10.1016/j.bmcl.2012.01.073.
Jun Chen 1 Miao-Miao Lu Bin Liu Zhuo Chen Qian-Bin Li Li-Jian Tao Gao-Yun Hu
Affiliations

Affiliation

  • 1 Department of Medicinal Chemistry, School of Pharmacy, Central South University, Changsha, Hunan Province, China.
Abstract

Pyridone compounds, such as pirfenidone (PFD) and fluorofenidone (AKF-PD), are multi-target anti-fibrotic agents. Using PFD and AKF-PD as the leading compounds, two series of novel (5-substituent)-2(1H)-pyridone compounds were synthesized with the purpose of maintaining multi-targeting property and overcoming the drawbacks of fast metabolism. These derivatives demonstrated good proliferation inhibiting activity against NIH3T3 cells by MTT assay with AKF-PD as the positive control. Compound 5b exhibited a high potent of anti-fibrosis with a IC(50) of 0.08 mmol/L about 34 times of AKF-PD. The SAR of pyridone derivatives as anti-fibrosis agents was also discussed.

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