Discovery, Synthesis of Myrtucommulone B Analogs as Soluble Epoxide Hydrolase Inhibitors and Their Biological Activities
mechanism involves elevating anti-inflammatory epoxyeicosatrienoic acids (EETs) and reducing proinflammatory dihydroxyeicosatrienoic acids (DHETs) by blocking sEH, thereby suppressing proinflammatory cytokines (TNF-α, IL-6). This study lays a foundation for developing myrtucommulone-based sEH inhibitors as novel anti-inflammatory/analgesic agents, particularly potential therapeutics for AP.
Authors
- Yu Zhang (ORCID: https://orcid.org/0000-0003-3179-0538)
- Kang Shuang-shuang
- Bolin Wang (ORCID: https://orcid.org/0000-0001-8364-0238)
- Yang X
- Jia-Rui Sun
Institutions
- Henan Academy of Agricultural Sciences (CN)
- ZheJiang Academy of Agricultural Sciences (CN)
- Hengyang Academy of Agricultural Sciences (CN)
- University of South China (CN)
Publication Details
- Journal
- Journal of Medicinal Chemistry
- Published
- 2026-04-21
- DOI
- https://doi.org/10.1021/acs.jmedchem.5c03313
- Primary Topic
- Eicosanoids and Hypertension Pharmacology
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Education Department of Hunan Province
- Natural Science Foundation of Hunan Province