1. Academic Validation
  2. Discovery of Marine Highly Congested Polycyclic Isodhilarane-Type Meroterpenoids as Potential Leads for Treating Liver Fibrosis by Activating the HSF1/AMPK Metabolic Axis

Discovery of Marine Highly Congested Polycyclic Isodhilarane-Type Meroterpenoids as Potential Leads for Treating Liver Fibrosis by Activating the HSF1/AMPK Metabolic Axis

  • J Med Chem. 2026 Feb 26;69(4):4346-4360. doi: 10.1021/acs.jmedchem.5c03055.
Zhongping Jiang 1 Yue Chen 1 Shouyuan Wu 2 Junjie Wang 1 Feifei Liu 1 Jin Liu 1 Congjun Xu 1 Wanshan Li 3 Yong Rao 1 Ling Huang 1
Affiliations

Affiliations

  • 1 Key Laboratory of Tropical Biological Resources of Ministry of Education and One Health Institute, School of Pharmaceutical Sciences, Hainan University, Haikou 570228, P. R. China.
  • 2 Western Guangdong Characteristic Biology and Medicine Engineering and Research Center, School of Chemistry and Chemical Engineering, Lingnan Normal University, Zhanjiang 524048, P. R. China.
  • 3 Key Laboratory of Tropical Medicinal Resource Chemistry of Ministry of Education and Key Laboratory of Tropical Medicinal Plant Chemistry of Hainan Province, College of Chemistry and Chemical Engineering, Hainan Normal University, Haikou, Hainan 571158, P. R. China.
Abstract

Isodhilarane-type meroterpenoids are a small group of meroterpenoids with highly congested polycyclic skeletons and a wide range of biological activities. However, its antiliver fibrosis actions are rarely reported. Presently, a total of 28 isodhilarane-type meroterpenoids, including nine new ones, were identified based on NMR-guided isolation. By cell-based high-throughput screening, compound 11 (6/7/6/5/6/5 ring system) was demonstrated as the most promising candidate, showing significant antiliver fibrosis activity (IC50 = 0.7 μM) and favorable metabolic stability. Mechanistic studies revealed that 11 significantly inhibits TGF-β1/Smad signaling-mediated fibrogenesis and cell proliferation in activated hepatic stellate cells via activating the central HSF1/AMPK metabolic axis, being more potent than the positive control pirfenidone. Correspondingly, 11 significantly ameliorates liver injury and liver fibrosis in CCl4-treated fibrotic mice. Our findings revealed that isodhilarane-type meroterpenoids represent a novel privileged scaffold with antifibrotic properties, also highlighting compound 11 as a promising candidate for the treatment of liver fibrosis.

Figures
Products