1. Academic Validation
  2. Discovery of THB Derivates as Ferroptosis Inhibitors for the Treatment of Acute Kidney Injury by Targeting VDAC

Discovery of THB Derivates as Ferroptosis Inhibitors for the Treatment of Acute Kidney Injury by Targeting VDAC

  • J Med Chem. 2025 Jun 12;68(11):11340-11364. doi: 10.1021/acs.jmedchem.5c00280.
Shengkuan Peng 1 Wenhao Zhang 2 Qiaoyi Sun 1 Wenqiang Zhang 1 Yadong Chen 1 Zhicheng Lv 3 Zhihang Fang 3 Xian Wei 4 Tao Lu 1 Guo Chen 2 Yu Jiao 1
Affiliations

Affiliations

  • 1 School of Science, China Pharmaceutical University, Nanjing 211198, P. R. China.
  • 2 School of Biopharmacy, China Pharmaceutical University, Nanjing 211198, P. R. China.
  • 3 School of Life Science and Technology, China Pharmaceutical University, Nanjing 211198, P. R. China.
  • 4 Department of Pharmacy, Youjiang Medical University for Nationalities, Baise 533000, P. R. China.
Abstract

Acute kidney injury (AKI), a clinical syndrome marked by high morbidity and mortality, remains a significant challenge due to the lack of effective therapeutic options. The accumulation of Fe2+ and Reactive Oxygen Species (ROS) in injured renal cells, which triggers Ferroptosis, play a key driver in the pathogenesis of AKI. In this study, tetrahydroberberine (THB), a natural product, was identified as a Ferroptosis inhibitor that targeted the voltage-dependent anion channel (VDAC). Through structural optimization, a series of THB derivatives were developed, among which 34a exhibited about 100-fold enhanced Ferroptosis inhibitory activity. Moreover, 34a significantly reduced ROS, Fe2+ and restored glutathione (GSH) below 20 nM. In vivo experiments confirmed that 34a effectively alleviated folic acid-induced AKI, accompanied by a reduction in key kidney injury markers. These results highlight the potential of 12-amino THB derivatives as novel Ferroptosis inhibitors and provide promising therapeutic strategies for AKI treatment.

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