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Chemmedchem|June 19, 2024
Azologs of the Fatty Acid Mimetic Drug Cinalukast Enable Light-Induced PPARα ActivationMinh Sai, Niels van Herwijnen, Daniel MerkJournal of Medicinal Chemistry|September 5, 2024
Development of Tailless Homologue Receptor (TLX) Agonist Chemical ToolsEmily C Hank, Minh Sai, Till Kasch, et al.Communications Chemistry|July 1, 2024
Development of Nurr1 agonists from amodiaquine by scaffold hopping and fragment growingMinh Sai, Emily C Hank, Hin-Man Tai, et al.Journal of Medicinal Chemistry|September 26, 2023
Structure-Guided Design of Nurr1 Agonists Derived from the Natural Ligand DihydroxyindoleMinh Sai, Jan Vietor, Moritz Kornmayer, et al.Journal of Medicinal Chemistry|January 18, 2024
Structure-Guided Design of a Highly Potent Partial RXR Agonist with Superior Physicochemical PropertiesMax Lewandowski, Melania Carmina, Loris Knümann, et al.Journal of Medicinal Chemistry|September 11, 2024
Tuning RXR Modulators for PGC1α RecruitmentFelix Nawa, Minh Sai, Jan Vietor, et al.European Journal of Medicinal Chemistry|March 1, 2025
Novel thiazolones for the simultaneous modulation of PPARγ, COX-2 and 15-LOX to address metabolic disease-associated portal inflammationMai S El-Shoukrofy, Azza Ismail, Reem H Elhamammy, et al.ACS Pharmacology & Translational Science|June 19, 2025
Multi-Target Glitazones for Modulating Peroxisome Proliferator-Activated Receptor-γ, Cyclooxygenase-2, and Carbonic Anhydrases for the Management of Metabolic DysfunctionPerihan A Elzahhar, Hisham A Nematalla, Malak A Abouayana, et al.Pageof 1