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(41 products)
- Aminopeptidase(67 products)
- CETP(18 products)
- Carbonic Anhydrase(178 products)
- Casein Kinase(130 products)
- DHFR(33 products)
- Decarboxylase(4 products)
- Dehydrogenase(269 products)
- FAAH(64 products)
- FXR(58 products)
- Factor Xa(80 products)
- Fatty Acid Synthase(32 products)
- Ferroptosis(215 products)
- GR(3 products)
- GSNOR(3 products)
- Glucokinase(54 products)
- HIF/HIF Prolyl-Hydroxylase(142 products)
- HMG-CoA Reductase(33 products)
- Hydroxylase(30 products)
- IDO(82 products)
- LDL(8 products)
- Lipase(97 products)
- Lipid(59 products)
- Lipoxygenase(124 products)
- MAO(87 products)
- MPO(2 products)
- NAMPT(36 products)
- P450(6 products)
- PAI-1(25 products)
- PDE(166 products)
- PED(1 products)
- PKM(15 products)
- PPAR(164 products)
- Phospholipase(82 products)
- ROR(42 products)
- Retinoid Receptor(29 products)
- SGK(11 products)
- Thioredoxin(12 products)
- Transferase(30 products)
- Transporter(42 products)
- UGT(4 products)
- Xanthine Oxidase (XO) Inhibitors(9 products)
Show 34 more subcategories
Found 8626 products of "Metabolism"
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Ercalcitriol
CAS:<p>Ercalcitriol, active Vitamin D2 metabolite, boosts immunity by regulating CAMP and DEFB4 genes against infections.</p>Formula:C28H44O3Purity:99.02%Color and Shape:SolidMolecular weight:428.65Melittin Acetate
<p>Melittin Acetate, a PLA2 activator, enhances low-weight PLA2 activity but not high-weight PLA2.</p>Formula:C133H233N39O33Purity:99.78%Color and Shape:SoildMolecular weight:2906.51Speract
CAS:<p>Speract, a peptide from sea urchin eggs, regulates sperm motility and stimulates sperm mitochondrial metabolism.</p>Formula:C38H57N11O14Purity:98%Color and Shape:SolidMolecular weight:891.93LDHA-IN-8
CAS:<p>LDHA-IN-8, an inhibitor, inhibits the proliferation of pancreatic and lung cancer cells, decreasing the intracellular lactate content and increasing ROS levels.</p>Formula:C15H14N4O2Purity:99.73%Color and Shape:SolidMolecular weight:282.3AP-III-a4 hydrochloride
CAS:<p>AP-III-a4 hydrochloride (ENOblock hydrochloride) is a direct enolase (enolase) inhibitor that inhibit metastasis and affect glucose homeostasis.</p>Formula:C31H44ClFN8O3Purity:98%Color and Shape:SolidMolecular weight:631.18Sphingolipid ceramide N-deacylase (SCDase)
CAS:<p>SCDase splits fatty acids from sphingosine in glycosphingolipids, forming lysoglycosphingolipids.</p>Color and Shape:SolidBilirubin oxidase
CAS:<p>Bilirubin oxidase (BOD), a multi-copper enzyme, converts bilirubin to biliverdin, reduces O2 to H2O, and aids porphyrin metabolism.</p>Color and Shape:Solidα-Glucosidase-IN-26
<p>α-Glucosidase-IN-26 (Compound 7i), with an IC50 value of 4.63 µM, functions as an α-glucosidase inhibitor and is utilized in research related to type 2 diabetes</p>Formula:C23H22ClN3O5Purity:98%Color and Shape:SolidMolecular weight:455.89RORγt inverse agonist 33
<p>RORγt inverse agonist 33 (compound (R)-D4) is an orally bioavailable RORγt inverse agonist with an IC50 of 21 nM, playing a significant role in rheumatoid arthritis research.</p>Formula:C27H37NO5SColor and Shape:SolidMolecular weight:487.651Diadenosine pentaphosphate pentaammonium
CAS:<p>Endogenous vasoactive dinucleotide isolated from thrombocytes; found in secretory vesicles across various cells.</p>Formula:C20H44N15O22P5Color and Shape:SolidMolecular weight:1001.524CK2-IN-13
<p>CK2-IN-13 (compound 12c) is a potent inhibitor of CK2, with an IC50 value of 5.8 nM, playing a significant role in cancer research.</p>Formula:C19H13Br2NO3Color and Shape:SolidMolecular weight:463.119Fluazifop-P-butyl
CAS:<p>Fluazifop-P-butyl is an arylophenoxypropionate group graminicide that functions as an inhibitor of acetyl-CoA carboxylase (ACCase)[1].</p>Formula:C19H20F3NO4Color and Shape:Light Yellow LiquidMolecular weight:383.361-Stearoyl-2-Adrenoyl-sn-glycero-3-PE
CAS:<p>Phospholipid with stearic acid at sn-1, adrenic acid at sn-2; less in older human hippocampal mitochondria.</p>Formula:C45H82NO8PColor and Shape:SolidMolecular weight:796.124TPT-004
<p>TPT-004, a TPH inhibitor, exhibits superior pharmacokinetic and pharmacodynamic properties, and demonstrates efficacy in preclinical models for attenuating</p>Color and Shape:Odour Solid4-Hydroxy Atorvastatin calcium salt
CAS:<p>4-Hydroxy Atorvastatin calcium salt is metabolised by cytochrome P450 CYP3A4 and has antimicrobial and anti-microbial activity.</p>Formula:C66H68CaF2N4O12Color and Shape:SolidMolecular weight:1187.34α-Glucosidase-IN-83
<p>α-Glucosidase-IN-83 (compound I-1) is a potent inhibitor of α-glucosidase, demonstrating an IC50 of 1.49 μg/mL. This compound effectively reduces blood glucose levels in vivo.</p>Formula:C25H20N4O6SColor and Shape:SolidMolecular weight:504.514α-Glucosidase-IN-79
<p>α-Glucosidase-IN-79 (Compound 4d9) is a non-competitive α-glucosidase inhibitor with an IC50 of 2.11 μM, demonstrating greater inhibitory potency than the existing α-glucosidase inhibitors Acarbose (IC50 of 327.0 μM) and HXH8r (IC50 of 15.32 μM). It exhibits no cytotoxicity on normal human liver cells (LO2) and shows good metabolic stability in rat plasma. α-Glucosidase-IN-79 holds promise for research in type 2 diabetes.</p>Formula:C21H22N2O5SColor and Shape:SolidMolecular weight:414.4752H-Cho-Arg (trifluoroacetate salt)
CAS:<p>2H-Cho-Arg, a cationic lipid, enables gene delivery into cells and shows cytotoxicity at 92.7 μg/ml.</p>Formula:C43H73F6N5O7Color and Shape:SolidMolecular weight:886.06DIPQUO hydrochloride
<p>DIPQUO hydrochloride: ALP activator (EC50=6.27μM, C2C12 cells), induces osteoblast differentiation via p38 MAPK-β.</p>Formula:C20H18ClN3OPurity:98.09%Color and Shape:SoildMolecular weight:351.83Calcium Channel antagonist 4
CAS:<p>Calcium Channel antagonist 4 is a voltage-gated calcium channel inhibitor (IC50 : 5-20 μM).</p>Formula:C23H26N2O4SPurity:98.09%Color and Shape:SolidMolecular weight:426.53
