1. Academic Validation
  2. Pterisolic Acid B is a Nrf2 Activator by Targeting C171 within Keap1-BTB Domain

Pterisolic Acid B is a Nrf2 Activator by Targeting C171 within Keap1-BTB Domain

  • Sci Rep. 2016 Jan 13:6:19231. doi: 10.1038/srep19231.
Ting Dong 1 2 Weilong Liu 1 2 Zhirong Shen 2 Lin Li 2 She Chen 2 Xiaoguang Lei 1 2
Affiliations

Affiliations

  • 1 Beijing National Laboratory for Molecular Sciences, Key Laboratory of Bioorganic Chemistry and Molecular Engineering of Ministry of Education, Department of Chemical Biology, College of Chemistry and Molecular Engineering, Synthetic and Functional Biomolecules Center, and Peking-Tsinghua Center for Life Sciences, Peking University, Beijing 100871 (China).
  • 2 National Institute of Biological Sciences (NIBS), Changping District, Beijing 102206 (China).
Abstract

The use of chemoprotective agents to minimize the side effects of the chemotherapy, primarily via activation of the Nrf2 pathway, is an emerging research field, which has attracted broad attention from both academia and pharmaceutical industry. Through high-throughput chemical screens we have disclosed that pterisolic acid B (J19), a naturally occuring diterpenoid, is an effective Nrf2 activator. We have also identified a more potent natural product analogue J19-1 by semisynthesis and the subsequent biochemical evaluations revealed that J19-1 activates the Nrf2 pathway by covalently modifying Cys171 of keap1, which inhibits Nrf2 degradation mediated by Keap1-Cul3 complexes. Ultimately, we have demonstrated that J19-1 shows significant cytoprotective effect against cisplatin-induced cytotoxicity in HKC cells.

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