Targeting Acute Myelogenous Leukemia Using Potent Human Dihydroorotate Dehydrogenase Inhibitors Based on the 2-Hydroxypyrazolo[1,5-a]pyridine Scaffold: SAR of the Biphenyl Moiety
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MEDS433 induces apoptosis in several AML cell lines (II). (A) MEDS433
Targeting Acute Myelogenous Leukemia Using Potent Human Dihydroorotate Dehydrogenase Inhibitors Based on the 2-Hydroxypyrazolo[1,5-a]pyridine Scaffold: SAR of the Biphenyl Moiety
DD1 is a Proteasome Inhibitor Used for Acute Myeloid Leukemia (AML) Research
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Potent human dihydroorotate dehydrogenase inhibitory activity of new quinoline-4-carboxylic acids derived from phenolic aldehydes: Synthesis, cytotoxicity, lipophilicity and molecular docking studies - ScienceDirect
PDF) Targeting Acute Myelogenous Leukemia Using Potent Human Dihydroorotate Dehydrogenase Inhibitors Based on the 2-Hydroxypyrazolo[1,5- a ]pyridine Scaffold: SAR of the Aryloxyaryl Moiety
DHODH and cancer: promising prospects to be explored, Cancer & Metabolism
Biochemical characterization of Mycobacterium tuberculosis dihydroorotate dehydrogenase and identification of a selective inhibitor - Alberti - 2023 - FEBS Letters - Wiley Online Library
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DHODH and cancer: promising prospects to be explored, Cancer & Metabolism
Recent advances of human dihydroorotate dehydrogenase inhibitors for cancer therapy: Current development and future perspectives - ScienceDirect