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European Journal of Medicinal Chemistry|March 31, 2018
Potent and selective aldo-keto reductase 1C3 (AKR1C3) inhibitors based on the benzoisoxazole moiety: application of a bioisosteric scaffold hopping approach to flufenamic acidAgnese Chiara Pippione, Irene Maria Carnovale, Davide Bonanni, et al.Bioorganic & Medicinal Chemistry Letters|October 30, 2012
Synthesis and biological evaluation of colchicine C-ring analogues tethered with aliphatic linkers suitable for prodrug derivatisationJérémie Fournier-Dit-Chabert, Victoria Vinader, Ana Rita Santos, et al.Journal of Medicinal Chemistry|November 27, 2012
Synthesis and biological evaluation of colchicine B-ring analogues tethered with halogenated benzyl moietiesLaura Cosentino, Mariano Redondo-Horcajo, Ying Zhao, et al.European Journal of Medicinal Chemistry|February 16, 2024
Structure-guided optimization of 3-hydroxybenzoisoxazole derivatives as inhibitors of Aldo-keto reductase 1C3 (AKR1C3) to target prostate cancerAgnese Chiara Pippione, Sandra Kovachka, Chiara Vigato, et al.Pageof 6