Desidrogenase
As desidrogenases são enzimas envolvidas nas reações de oxidação-redução das vias metabólicas, desempenhando um papel central na produção de energia e na respiração celular. Estas enzimas são cruciais para processos como o ciclo do ácido cítrico, a glicólise e a oxidação dos ácidos graxos. Os inibidores de desidrogenases são ferramentas importantes no estudo de doenças metabólicas, câncer e estresse oxidativo. Na CymitQuimica, oferecemos uma seleção abrangente de inibidores de desidrogenases para apoiar sua pesquisa em metabolismo, biologia do câncer e bioquímica.
Foram encontrados 302 produtos de "Desidrogenase"
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Tiazofurin
CAS:Tiazofurin, a synthetic nucleoside, has anti-cancer effects and inhibits IMPDH as TAD after metabolism.Fórmula:C9H12N2O5SPureza:99.91%Cor e Forma:SolidPeso molecular:260.27BMS-823778 hydrochloride
CAS:BMS-823778 hydrochloride is a potent, selective, and orally active inhibitor of 11β-HSD1 (11β-Hydroxysteroid Dehydrogenase Type 1), demonstrating an IC50 (half
Fórmula:C18H19Cl2N3OCor e Forma:SolidPeso molecular:364.27Perfluorooctanoic acid
CAS:Perfluorooctanoic acid (PFOA) (PFOA) is a persistent and widespread industry-made chemical.Fórmula:C8HF15O2Pureza:99.70%Cor e Forma:White To Off-White Powder OthersolidPeso molecular:414.07Ref: TM-T9333
5mg52,00€10mg78,00€25mg119,00€50mg172,00€100mg259,00€200mg388,00€500mg642,00€1mL*10mM (DMSO)77,00€MK-8245
CAS:MK-8245 is a liver-targeting SCD inhibitor for human SCD1 (IC50: 1 nM) and for rat/mouse SCD1 (IC50: 3 nM), with anti-diabetic and anti-dyslipidemic function.Fórmula:C17H16BrFN6O4Pureza:97.58% - 99%Cor e Forma:SolidPeso molecular:467.25Ref: TM-T2650
1mg37,00€5mg90,00€10mg144,00€25mg259,00€50mg440,00€100mg615,00€200mg853,00€1mL*10mM (DMSO)92,00€AZD7545
CAS:AZD7545 is a potent PDHK inhibitor.Fórmula:C19H18ClF3N2O5SPureza:99.12% - 99.96%Cor e Forma:SolidPeso molecular:478.87NCT-501 hydrochloride
CAS:NCT-501 hydrochloride: potent, selective ALDH1A1 inhibitor based on theophylline; IC50 of 40 nM; highly discriminant against other ALDHs.Fórmula:C21H33ClN6O3Cor e Forma:SolidPeso molecular:452.98NCT-501
CAS:NCT-501 is a potent and selective inhibitor of Aldehyde Dehydrogenase 1A1 (ALDH1A1) with IC50 of 40 nM.Fórmula:C21H32N6O3Pureza:99.19%Cor e Forma:SolidPeso molecular:416.523-Hydroxybenzaldehyde
CAS:3-Hydroxybenzaldehyde is a compound useful in organic synthesis.Fórmula:C7H6O2Pureza:99.60%Cor e Forma:DrypowderPeso molecular:122.12NCT-503
CAS:NCT-503 is a phosphoglycerate dehydrogenase (PHGDH) inhibitor with no activity against other dehydrogenases. NCT-503 has antitumor activity. Cost-effective and quality-assured.Fórmula:C20H23F3N4SPureza:98.91% - 99.84%Cor e Forma:SolidPeso molecular:408.48Ref: TM-T4213
2mg39,00€5mg59,00€10mg95,00€25mg177,00€50mg321,00€100mg477,00€200mg667,00€1mL*10mM (DMSO)65,00€L-Allylglycine
CAS:L-Allylglycine is a potent inhibitor of the synthetic enzyme for GABA, glutamic acid decarboxylase.Fórmula:C5H9NO2Pureza:≥98%Cor e Forma:White To Off-White Crystalline PowderPeso molecular:115.13AKR1C3-IN-4
CAS:AKR1C3-IN-4: potent, selective AKR1C3 inhibitor, IC50 = 0.56 μM, potential for CRPC research.Fórmula:C14H10F3NO2Pureza:98.59%Cor e Forma:SolidPeso molecular:281.23LDHA-IN-4
CAS:LDHA-IN-4 (AZ33) is an LDHA inhibitor. Binding affinity to 6-His-tagged human LDHA expressed in E.coli BL21 (DE3) by SPR analysis with an active value of 93 nM.Fórmula:C25H27N3O6SPureza:98.17% - 99.68%Cor e Forma:SolidPeso molecular:497.56Mutant IDH1-IN-1
CAS:Mutant IDH1-IN-1 is a potent mutant IDH1 R132 h inhibitor with IC50 < 0.1 uM.Fórmula:C30H31FN4O2Pureza:99.49% - >99.99%Cor e Forma:SolidPeso molecular:498.59Ref: TM-T2043
2mg44,00€5mg67,00€10mg94,00€25mg173,00€50mg249,00€100mg363,00€200mg490,00€1mL*10mM (DMSO)71,00€CM10
CAS:CM10 is an aldehyde dehydrogenase 1A family(ALDH1A) inhibitor.Fórmula:C20H23N3OPureza:99.84%Cor e Forma:SolidPeso molecular:321.42AKR1C3-IN-1
CAS:AKR1C3-IN-1 is a potent and selective inhibitor of AKR1C3(IC50 of 13 nM).Fórmula:C16H15NO4SPureza:98.02%Cor e Forma:SolidPeso molecular:317.36VER-246608
CAS:VER-246608 inhibits PDK (IC50: 35-91 nM), boosts PDC, reduces glycolysis, causes cancer cell cytostasis, and enhances doxorubicin effects.Fórmula:C28H23ClF2N4O4Pureza:98.5%Cor e Forma:SolidPeso molecular:552.96Ref: TM-T17224
1mg50,00€2mg71,00€5mg105,00€10mg166,00€25mg313,00€50mg475,00€100mg692,00€1mL*10mM (DMSO)130,00€AG-636
CAS:AG-636 is a potent, reversible, selective and orally active DHODH inhibitor(IC50 of 17 nM). It has strong anticancer effects.Fórmula:C21H17N3O2Pureza:99.19%Cor e Forma:SolidPeso molecular:343.38Nitrofen
CAS:Nitrofen is a selective contact herbicide. Nitrofen is a protoporphyrinogen oxidase and retinal dehydrogenase inhibitor.Fórmula:C12H7Cl2NO3Pureza:99.92%Cor e Forma:Less Crystals Or Black Solid Used As A Pre- Or Post-Emergence HerbicidePeso molecular:284.09Carbenoxolone disodium
CAS:Carbenoxolone disodium treats stomach ulcers; derived from licorice, often has antidiuretic effects, low toxicity.Fórmula:C34H48Na2O7Pureza:99.69%Cor e Forma:SolidPeso molecular:614.72Vidofludimus hemicalcium
CAS:Vidofludimus hemicalcium: oral DHODH inhibitor, FXR modulator, for autoimmune and fatty liver research.Fórmula:C20H18FNO4CaCor e Forma:SolidPeso molecular:375.4
