Structure activity relationship of flavonoids as PPARγ agonists
Abstract Peroxisome proliferator-activated receptor γ (PPARγ) is a transcriptional factor and key regulatory element in glucose and lipid metabolism. We have attempted to determine the structure–activity relationship between flavonoids as PPARγ agonists through a literature search. To compare results from different studies and methods, we have recalculated them to the percentage of positive control (% PC ). We have also described various methods used to determine PPARγ agonists. The most promising PPARγ agonists are isoflavones, namely 4'-fluoro-7-hydroxyisoflavone ( 4 ; % PC = 710.3%). The results presented in this review could be used for further semisynthetic modifications of flavonoids to enhance their PPARγ agonistic activity.
Authors
- Peter Kubatka (ORCID: https://orcid.org/0000-0003-4312-5076)
- Jakub Treml (ORCID: https://orcid.org/0000-0002-8690-9981)
- Daniela Nykodýmová (ORCID: https://orcid.org/0000-0002-7189-2398)
Institutions
- University of Veterinary Sciences Brno (CZ)
- Masaryk University (CZ)
- Comenius University Bratislava (SK)
Publication Details
- Journal
- Phytochemistry Reviews
- Published
- 2025-04-29
- DOI
- https://doi.org/10.1007/s11101-025-10121-w
- Citations
- 1
- Primary Topic
- Peroxisome Proliferator-Activated Receptors
- Type
- article
- Field-Weighted Citation Impact
- 0.81
Funders
- Masarykova Univerzita