Dihydroorotate dehydrogenase inhibitors in anti-infective drug research

Targeting Myeloid Differentiation Using Potent 2-Hydroxypyrazolo[1,5-a]pyridine Scaffold-Based Human Dihydroorotate Dehydrogenase Inhibitors

Design, synthesis, biological evaluation and X-ray structural studies of potent human dihydroorotate dehydrogenase inhibitors based on hydroxylated azole scaffolds

Bioisosteres of Indomethacin as Inhibitors of Aldo-Keto Reductase 1C3

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

NO-Donor Phenols: A New Class of Products Endowed with Antioxidant and Vasodilator Properties