Publication | Open Access

Potent and selective aldo-keto reductase 1C3 (AKR1C3) inhibitors based on the benzoisoxazole moiety: application of a bioisosteric scaffold hopping approach to flufenamic acid

Bioisosteric ScaffoldMedicinal ChemistryPharmaceutical ScienceBiochemistryMedicineNatural SciencesBenzoisoxazole MoietyRational Drug DesignPharmacotherapyAnti-cancer AgentDrug DevelopmentChemical BiologyPharmacologyPharmaceutical ChemistryDrug Discovery