Metabolism
Metabolism inhibitors are compounds that interfere with metabolic pathways, altering the production and utilization of energy within cells. These inhibitors are used to study the regulation of metabolism, the role of metabolic pathways in diseases like cancer and diabetes, and to develop new therapeutic strategies. Metabolism inhibitors can target various enzymes and processes involved in glycolysis, fatty acid oxidation, and other metabolic functions. At CymitQuimica, we offer a wide range of high-quality metabolism inhibitors to support your research in biochemistry, metabolic disorders, and drug development.
Subcategories of "Metabolism"
- AhR(42 products)
- Aminopeptidase(76 products)
- CETP(20 products)
- Carbonic Anhydrase(196 products)
- Casein Kinase(138 products)
- DHFR(30 products)
- Decarboxylase(4 products)
- Dehydrogenase(302 products)
- FAAH(64 products)
- FXR(62 products)
- Factor Xa(87 products)
- Fatty Acid Synthase(37 products)
- Ferroptosis(227 products)
- GR(3 products)
- GSNOR(3 products)
- Glucokinase(56 products)
- HIF/HIF Prolyl-Hydroxylase(146 products)
- HMG-CoA Reductase(34 products)
- Hydroxylase(36 products)
- IDO(84 products)
- LDL(7 products)
- Lipase(107 products)
- Lipid(62 products)
- Lipoxygenase(133 products)
- MAO(86 products)
- MPO(2 products)
- NAMPT(40 products)
- P450(6 products)
- PAI-1(26 products)
- PDE(170 products)
- PED(1 products)
- PKM(17 products)
- PPAR(170 products)
- Phospholipase(85 products)
- ROR(47 products)
- Retinoid Receptor(20 products)
- SGK(10 products)
- Thioredoxin(12 products)
- Transferase(30 products)
- Transporter(43 products)
- UGT(4 products)
- Xanthine Oxidase (XO) Inhibitors(9 products)
Show 34 more subcategories
Found 9207 products of "Metabolism"
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ICMT-IN-36
CAS:ICMT-IN-36 (compound 40) serves as an ICMT inhibitor, with an IC50 value of 0.181 μM [1].Formula:C21H25Cl2NOColor and Shape:SolidMolecular weight:378.34HSD17B13-IN-3
CAS:HSD17B13-IN-3 (compound 2) is a potent inhibitor of hydroxysteroid 17ß-dehydrogenase 13 (HSD17B13), lacking cellular experimental activity [1].Formula:C22H21NO6S2Color and Shape:SolidMolecular weight:459.541-Deazaadenosine
CAS:1-Deazaadenosine, an adenosine deaminase inhibitor (Ki: 0.66 μM), may treat cancer, particularly lymphoproliferative disorders.Formula:C11H14N4O4Purity:98%Color and Shape:SolidMolecular weight:266.25NTE-122
CAS:NTE-122 is a competitive Acyl-CoA:cholesterol acyltransferase (ACAT) inhibitor.Formula:C38H59ClN6O2Purity:98%Color and Shape:SolidMolecular weight:667.38CKD-519
CAS:CKD-519: A CETP inhibitor with an IC50 of 2.3 nM, blocking cholesteryl ester transfer in serum.Formula:C31H34F7NO3Color and Shape:SolidMolecular weight:601.6Perindopril acyl-β-D-glucuronide
CAS:Perindopril acyl-β-D-glucuronide is a metabolite of the ACE inhibitor perindopril [1].Formula:C25H40N2O11Purity:98%Color and Shape:SolidMolecular weight:544.59hCAIX-IN-16
CAS:hCAIX-IN-16 (Compound 12d), an inhibitor of hCA IX, exhibits inhibition constants (K i) of 190.0 nM for hCA IX and 187.9 nM for hCA XII.Formula:C20H20N8O2SPurity:98%Color and Shape:SolidMolecular weight:436.49(Rac)-CP-609754
CAS:LNK754 is a farnesyltransferase inhibitor. It is used for the treatment of cancer and Alzheimer's disease.Formula:C29H22ClN3O2Purity:98%Color and Shape:SolidMolecular weight:479.96VU0364739
CAS:VU0364739, a selective phospholipase D2 (PLD2) inhibitor with an IC50 of 22 nM, effectively reduces cancer cell proliferation [1].Formula:C26H27FN4O2Purity:98%Color and Shape:SolidMolecular weight:446.52BMS-986172
CAS:BMS-986172 is an orally active, highly selective inhibitor of MGAT2, demonstrating inhibitory concentrations (IC50) of 4.6 nM for human MGAT2 (hMGAT2) and 20 nMFormula:C24H22F7N7O3Purity:98%Color and Shape:SolidMolecular weight:589.471-Isopropyltryptophan
CAS:1-Isopropyltryptophan (1-IsoPT), an IDO1 inhibitor, suppresses the expression of IDO-1 and IDO-2 mRNA induced by IFN-γ stimulation [1].Formula:C14H18N2O2Purity:98%Color and Shape:SolidMolecular weight:246.3PHD-IN-1
CAS:PHD-IN-1 (compound 80) serves as a potent PHD2 inhibitor, exhibiting an IC50 value of ≤5 nM.Formula:C24H23N7O2Purity:98%Color and Shape:SolidMolecular weight:441.49IDO1/TDO-IN-6
CAS:IDO1/TDO-IN-6 (compound 11) is a dual inhibitor targeting IDO1 and TDO, exhibiting IC50 values of 2.25 μM for IDO1 and 2.89 μM for TDO.Formula:C20H17NO5Purity:98%Color and Shape:SolidMolecular weight:351.35PHD-IN-2
CAS:PHD-IN-2 (Compound 91), a potent PHD antagonist with an IC50 of less than 5 nM, effectively stimulates erythropoietin synthesis in HEP3B cells with an EC50 ofFormula:C26H27N7O4Purity:98%Color and Shape:SolidMolecular weight:501.54N-Methyl Palbociclib
CAS:N-Methyl Palbociclib is an impurity of the orally active selective CDK4 and CDK6 inhibitor Palbociclib (PD 0332991).Formula:C25H31N7O2Purity:98%Color and Shape:SolidMolecular weight:461.561-Palmitoyl-2-Oleoyl-sn-glycero-3-PA
CAS:1-Palmitoyl-2-oleoyl-sn-glycero-3-PA (1,2-POPA) is a phospholipid featuring a palmitic acid (16:0) chain that is saturated and an oleic acid (18:1) chain that is monounsaturated, positioned at the sn-1 and sn-2 locations, respectively. This compound is utilized in creating micelles, liposomes, and various artificial membrane forms.Formula:C37H71O8PColor and Shape:SolidMolecular weight:674.9Quizalofop
CAS:Quizalofop (Xylafop) is a reagent of biochemical.Formula:C17H13ClN2O4Purity:97.14%Color and Shape:SolidMolecular weight:344.75Ref: TM-T19959
5mg52.00€10mg73.00€25mg105.00€50mg156.00€100mg224.00€500mg557.00€1mL*10mM (DMSO)65.00€EMT inhibitor-2
CAS:EMT inhibitor-2 blocks CYP3A4 and CYP2C9 (IC50: 49.72, 5.54 μM) and prevents IL-1β/TGF-β-induced EMT.Formula:C24H26N2O8Color and Shape:SolidMolecular weight:470.47LFHP-1c
CAS:LFHP-1c, a neuroprotective PGAM5 inhibitor, demonstrates efficacy in preserving blood-brain barrier integrity following ischemic stroke.Formula:C55H64N6O4Purity:98.07%Color and Shape:SolidMolecular weight:873.13Homonojirimycin
CAS:Homonojirimycin is an alpha-glucosidase inhibitor.Formula:C7H15NO5Purity:98%Color and Shape:SolidMolecular weight:193.2
