Dehydrogenase
Dehydrogenases are enzymes involved in the oxidation-reduction reactions of metabolic pathways, playing a central role in energy production and cellular respiration. These enzymes are crucial for processes such as the citric acid cycle, glycolysis, and fatty acid oxidation. Dehydrogenase inhibitors are important tools in the study of metabolic diseases, cancer, and oxidative stress. At CymitQuimica, we provide a comprehensive selection of dehydrogenase inhibitors to support your research in metabolism, cancer biology, and biochemistry.
Found 322 products for "Dehydrogenase".
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XEN723
CAS:XEN723 is a potent thiazolylimidazolidinone Stearoyl-CoA Desaturase (SCD1) inhibitor(IC50s of 45 and 524 nM in mouse and HepG2 cell, respectively).Formula:C21H20FN5O2SPurity:99.5%Color and Shape:SolidMolecular weight:425.479GSK2837808A
CAS:GSK2837808A is a potent and selective inhibitor of lactate dehydrogenase A (LDHA) (IC50s: 1.9 and 14 nM for LDHA and LDHB, respectively).Formula:C31H25F2N5O7SPurity:99.78% - 99.78%Color and Shape:SolidMolecular weight:649.62CVT-10216
CAS:CVT-10216 inhibits ALDH2 (IC50: 29 nM) and ALDH-1 (IC50: 1.3 μM), reducing alcohol intake and anxiety in rats.Formula:C24H19NO7SPurity:98.76%Color and Shape:SolidMolecular weight:465.48KPLH1130
CAS:KPLH1130, a PDK inhibitor, boosts glucose tolerance and reduces inflammation in high-fat diet mice.Formula:C15H13N3O3Purity:99.07%Color and Shape:SolidMolecular weight:283.282MF-438
CAS:MF-438 is an effective and orally bioavailable stearoyl-CoA desaturase 1 (SCD1) inhibitor (EC50: 2.3 nM for rSCD1).Formula:C19H18F3N5OSPurity:98.98% - 99.50%Color and Shape:SolidMolecular weight:421.44TC HSD 21
CAS:TC HSD 21 is a potent and highly selective inhibitor of 17β-hydroxysteroid dehydrogenase type 3 (IC50 = 14 nM).Formula:C17H12BrNO3S2Purity:99.32%Color and Shape:SolidMolecular weight:422.32LY 345899
CAS:LY 345899 is a Folate analog and is a methylenetetrahydrofolate dehydrogenase and MTHFD2 inhibitor (IC50: 96 nM and 663 nM, respectively and a Ki: 18 nM forFormula:C20H21N7O7Purity:99.7%Color and Shape:SolidMolecular weight:471.4234ML390
CAS:ML390 exerts its potent differentiation effect on multiple leukemia models.Formula:C21H21F3N2O3Purity:99.76%Color and Shape:SolidMolecular weight:406.40Mycophenolic acid
CAS:Mycophenolic acid (Mycophenolate) is an inosine monophosphate dehydrogenase(IMPDH) inhibitor with anti-proliferative activity.Formula:C17H20O6Purity:99.27% - 99.8%Color and Shape:White SolidMolecular weight:320.3371LDH-IN-1
CAS:LDH-IN-1 is a pyrazole-based human lactate dehydrogenase (LDH) inhibitor(IC50s of 32 and 27 nM for LDHA and LDHB, respectively).Formula:C30H26N4O4S2Purity:99.6%Color and Shape:SolidMolecular weight:570.68PTC299
CAS:PTC299 ((4-chlorophenyl) (1S)-6-chloro-1-(4-methoxyphenyl)-1,3,4,9-tetrahydropyrido[3,4-b]indole-2-carboxylate) is an orally active inhibitor of VEGFA mRNAFormula:C25H20Cl2N2O3Purity:99.72%Color and Shape:White SolidMolecular weight:467.34CBR-5884
CAS:CBR-5884: active PHGDH inhibitor, IC50=33μM, disrupts serine synthesis, selectively targets high-serine cancers.Formula:C14H12N2O4S2Purity:99.97%Color and Shape:SolidMolecular weight:336.39SCD1 inhibitor-4
CAS:SCD1 inhibitor-4 is stearoylCoA desaturase-1 (SCD1) inhibitor. SCD1 inhibitor-4 can be used for the research of diabetes.Formula:C17H16F3N5OPurity:99.71%Color and Shape:SolidMolecular weight:363.337Mutant IDH1 inhibitor
CAS:Mutant IDH1 inhibitor is an effective inhibitor of mutant IDH1 R132H (IC50: < 72 nM).Formula:C25H34N6O3Purity:98.3%Color and Shape:SolidMolecular weight:466.5759NCT-502
CAS:NCT-502 (N-(4,6-dimethylpyridin-2-yl)-4-[5-(trifluoromethyl)pyridin-2-yl]piperazine-1-carbothioamide) is a human phosphoglycerate dehydrogenase inhibitor,Formula:C18H20F3N5SPurity:99.60%Color and Shape:Yellow SolidMolecular weight:395.45DHODH-IN-11
CAS:DHODH-IN-11 is a leflunomide derivative and weak dihydroorotate dehydrogenase (DHODH) inhibitor with a pKa of 5.03.Formula:C15H11N3O2Purity:98.14%Color and Shape:SolidMolecular weight:265.27BAY-2402234
CAS:BAY-2402234: a selective DHODH inhibitor targeting myeloid cancers with low-nanomolar potency.Formula:C21H18ClF5N4O4Purity:98.9%Color and Shape:SolidMolecular weight:520.84CAY10566
CAS:CAY10566 is a potent SCD1 inhibitor, orally bioavailable, with IC50s: HepG2 cells, 7.9nM; mouse, 4.5nM; human, 26nM.Formula:C18H17ClFN5O2Purity:99.54% - 99.75%Color and Shape:SolidMolecular weight:389.811IDH-305
CAS:IDH-305: Oral, mutation-specific IDH1 inhibitor, 200x selective for R132 mutants; IC50: 27/28/6.14 nM for R132H/C/WT.Formula:C23H22F4N6O2Purity:99.68%Color and Shape:SolidMolecular weight:490.45344-Diethylaminobenzaldehyde
CAS:4-Diethylaminobenzaldehyde: reversible ALDH1 inhibitor (Ki: 4 nM), potent anti-androgen (IC50: 1.71μM).Formula:C11H15NOPurity:99.6%Color and Shape:Brown-Black CrystalsMolecular weight:177.2429
