Deshidrogenasa
Las deshidrogenasas son enzimas involucradas en las reacciones de oxidación-reducción de las vías metabólicas, desempeñando un papel central en la producción de energía y la respiración celular. Estas enzimas son cruciales para procesos como el ciclo del ácido cítrico, la glucólisis y la oxidación de ácidos grasos. Los inhibidores de deshidrogenasas son herramientas importantes en el estudio de enfermedades metabólicas, cáncer y estrés oxidativo. En CymitQuimica, ofrecemos una selección completa de inhibidores de deshidrogenasas para apoyar su investigación en metabolismo, biología del cáncer y bioquímica.
Se han encontrado 270 productos de "Deshidrogenasa"
Ordenar por
Pureza (%)
0
100
|
0
|
50
|
90
|
95
|
100
hDHODH-IN-9
CAS:<p>hDHODH-IN-9 is a potent hDHODH inhibitor, IC50=0.34 μM, toxic to MCF-7/A375 cells, promising for cancer research.</p>Fórmula:C21H21NO4Forma y color:SolidPeso molecular:351.4GA11
CAS:<p>GA11is an inhibitor of ALDH1. It also displays anti-GBM effects in vitro and in vivo.</p>Fórmula:C19H14N2Pureza:98%Forma y color:SolidPeso molecular:270.33IGP-1
CAS:<p>iGP-1 is a cell-permeable mitochondrial sn-Glycerol 3-phosphate dehydrogenase (mGPDH) inhibitor.</p>Fórmula:C17H15N3O3Pureza:99.12% - 99.15%Forma y color:SolidPeso molecular:309.32ALDH1A3-IN-2
CAS:<p>ALDH1A3-IN-2 is a potent ALDH1A3 inhibitor with an IC50 of 0.30 μM.ALDH1A3-IN-2 has potential for cancer disease research.</p>Fórmula:C13H17NOPureza:99.84%Forma y color:SolidPeso molecular:203.28DS18561882
CAS:<p>DS18561882: Potent MTHFD2 inhibitor (IC50=0.0063), inhibits MTHFD1 (IC50=0.57), good oral kinetics.</p>Fórmula:C28H31F3N4O6SPureza:98.19% - >99.99%Forma y color:SolidPeso molecular:608.63DSM421
CAS:<p>DSM421 (DSM-421) is a dihydrodehydrogenase inhibitor (DHODH) that is in preclinical development as a potential treatment option for malaria and has shown</p>Fórmula:C14H11F5N6Pureza:98.23% - 99.82%Forma y color:SolidPeso molecular:358.27G6PD activator AG1
CAS:<p>G6PD activator AG1 is a G6PD agonist that promotes G6PD oligomerization to a catalytically competent form.</p>Fórmula:C24H30N4S2Pureza:98.38% - 99.51%Forma y color:SolidPeso molecular:438.65CM037
CAS:<p>CM037 (A-37) is a selective ALDH1A1 (acetaldehyde dehydrogenase 1A1) inhibitor (IC50; 4.6 µM) with antitumor activity and may be used in studies to eliminate</p>Fórmula:C21H25N3O3S2Pureza:99.34%Forma y color:SolidPeso molecular:431.57IMPDH2-IN-2
CAS:<p>IMPDH2-IN-2 is an IMPDH inhibitor with antimicrobial activity and potential anti-tuberculosis activity for the study of inflammation and immune dysfunction.</p>Fórmula:C21H15Cl2N3O3Pureza:99.02%Forma y color:SolidPeso molecular:428.27PHGDH-IN-3
CAS:<p>PHGDH-IN-3, an oral PHGDH blocker with 2.8 μM IC50, may help in cancer research.</p>Fórmula:C24H18FN3O4S2Pureza:97.24% - 98.55%Forma y color:SolidPeso molecular:495.55Olorofim
CAS:<p>Olorofim（F-901318）is a new selective antifungal compound that inhibits Aspergillus fumigatus DHODH (IC50: 44 nM). Cost-effective and quality-assured.</p>Fórmula:C28H27FN6O2Pureza:99.28%Forma y color:SolidPeso molecular:498.55CPS-11
CAS:<p>CPS-11, a Thalidomide analogue, shows potent, broad antitumor activity, especially in multiple myeloma cells.</p>Fórmula:C14H12N2O5Pureza:99.8% - 99.98%Forma y color:SolidPeso molecular:288.26PKUMDL-WQ-2101
CAS:<p>PKUMDL-WQ-2101 is a selective allosteric inhibitor of phosphoglycerate dehydrogenase with anti-tumor activity.</p>Fórmula:C14H11N3O6Pureza:99.57%Forma y color:SolidPeso molecular:317.25hDHODH-IN-7
CAS:<p>hDHODH-IN-7 (DHODH-IN-9) is a nitrogen-containing analog and is a human dihydrorotatory dehydrogenase inhibitor.</p>Fórmula:C21H23FN4OPureza:99.87%Forma y color:SolidPeso molecular:366.43Qc1
CAS:<p>Qc1 is an inhibitor of threonine dehydrogenase (TDH) inhibitor and can be used in studies about metabolic diseases.</p>Fórmula:C23H16F3N3O2SPureza:99.75%Forma y color:SolidPeso molecular:455.45IDH2R140Q-IN-2
CAS:<p>IDH2R140Q-IN-2 is an IDH2R140Q inhibitor indicated for the study of acute myeloid leukaemia (AML).</p>Fórmula:C21H18F6N6OPureza:99.92%Forma y color:SolidPeso molecular:484.4BMS-823778
CAS:<p>BMS-823778 is a potent inhibitor of 11β-hydroxysteroid dehydrogenase type 1 (11β-HSD-1) for the study of type 2 diabetes.</p>Fórmula:C18H18ClN3OPureza:99.39% - 99.75%Forma y color:SolidPeso molecular:327.81HSD-016
CAS:<p>HSD-016: Oral 11β-HSD1 inhibitor, active in humans, mice, rats (IC50: 11, 1, 8 nM), potential for type 2 diabetes research.</p>Fórmula:C21H21F7N2O3SPureza:99.40% - >99.99%Forma y color:SolidPeso molecular:514.46HSD17B13-IN-3
CAS:<p>HSD17B13-IN-3 (compound 2) is a potent inhibitor of hydroxysteroid 17ß-dehydrogenase 13 (HSD17B13), lacking cellular experimental activity [1].</p>Fórmula:C22H21NO6S2Forma y color:SolidPeso molecular:459.54Anticancer agent 121
CAS:<p>Anticancer agent 121, a human lactate dehydrogenase A (hLDHA) inhibitor, exhibits potent anticancer activities, suitable for use in anticancer research [1].</p>Fórmula:C19H18N2O3SForma y color:SolidPeso molecular:354.42
