Métabolisme
Les inhibiteurs du métabolisme sont des composés qui interfèrent avec les voies métaboliques, modifiant ainsi la production et l'utilisation de l'énergie au sein des cellules. Ces inhibiteurs sont utilisés pour étudier la régulation du métabolisme, le rôle des voies métaboliques dans des maladies telles que le cancer et le diabète, et pour développer de nouvelles stratégies thérapeutiques. Les inhibiteurs du métabolisme peuvent cibler diverses enzymes et processus impliqués dans la glycolyse, l'oxydation des acides gras et d'autres fonctions métaboliques. Chez CymitQuimica, nous offrons une large gamme d'inhibiteurs de métabolisme de haute qualité pour soutenir vos recherches en biochimie, troubles métaboliques et développement de médicaments.
Sous-catégories appartenant à la catégorie "Métabolisme"
- AhR(42 produits)
- Aminopeptidase(76 produits)
- CETP(20 produits)
- Anhydrase carbonique(197 produits)
- Caséine Kinase(137 produits)
- DHFR(34 produits)
- Décarboxylase(4 produits)
- Déshydrogénase(302 produits)
- FAAH(66 produits)
- FXR(62 produits)
- Facteur Xa(87 produits)
- Synthase des acides gras(37 produits)
- Ferroptose(226 produits)
- GR(3 produits)
- GSNOR(4 produits)
- Glucokinase(57 produits)
- Prolyl-Hydroxylase de HIF/HIF(146 produits)
- HMG-CoA Réductase(33 produits)
- Hydroxylase(35 produits)
- IDO(84 produits)
- LDL(8 produits)
- Lipase(107 produits)
- Lipides(61 produits)
- Lipoxygénase(134 produits)
- MAO(87 produits)
- MPO(2 produits)
- NAMPT(40 produits)
- P450(6 produits)
- PAI-1(26 produits)
- PDE(167 produits)
- PED(1 produits)
- PKM(17 produits)
- PPAR(169 produits)
- Phospholipase(83 produits)
- ROR(47 produits)
- Récepteur de rétinoïdes(28 produits)
- SGK(11 produits)
- Thioredoxine(12 produits)
- Transférase(29 produits)
- Tansporteur(46 produits)
- UGT(4 produits)
- Inhibiteurs de la xanthine oxydase (XO)(9 produits)
Affichez 34 plus de sous-catégories
9280 produits trouvés pour "Métabolisme"
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Sphingomyelin (d18:1/12:0)
CAS :Sphingomyelin (d18:1/12:0) is a polar lipid known for its role in modulating cell signal transduction. It plays a critical role in cell membranes, influencing their fluidity and stability. Additionally, sphingomyelin (d18:1/12:0) is involved in lipid metabolism and has potential in promoting neuronal cell growth. This compound is essential for the functioning and development of the nervous system.Formule :C35H71N2O6PCouleur et forme :SolidMasse moléculaire :646.92Lufironil
CAS :Lufironil (HOE 077) is an inhibitor of prolyl 4-hydroxylase, designed for investigating chronic liver conditions such as alcoholic hepatitis and cirrhosis.Formule :C13H19N3O4Couleur et forme :SolidMasse moléculaire :281.311-Stearoyl-sn-glycerol 3-phosphate sodium
CAS :1-Stearoyl-sn-glycerol 3-phosphate sodium, a biologically active phospholipid, plays a crucial role in regulating cell motility, proliferation, invasion, survival, and the production of growth factors through interactions with G protein-coupled receptors (GPCR). Synthesized during the formation of membrane phospholipids, this compound typically has a low plasma concentration (approximately 100nM) and originates from various cell types, including activated platelets, epithelial cells, leukocytes, neuronal cells, and tumor cells. Its distinctive structure features stearic acid at the sn-1 position and a hydroxyl group at the sn-2 position.Formule :C21H42NaO7PCouleur et forme :SolidMasse moléculaire :460.52ATUX-8385
CAS :ATUX-8385 is a potent activator of PP2A. It binds to the PR65 subunit and holds promise for research into cancer and chronic diseases, including Alzheimer's disease and chronic obstructive pulmonary disease (COPD).Formule :C24H20F5N3O4SCouleur et forme :SolidMasse moléculaire :541.49Anticancer agent 143
CAS :Anticancer Agent 143 (Compound 369), a potent dual inhibitor targeting PTPN2 and PTP1B, exhibits IC50 values below 2.5 nM.Formule :C19H15BrF2N3O6PS2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :594.34Magnesium ionophore III
CAS :Magnesium ionophore III (ETH 4030) is an ion carrier that regulates intracellular magnesium ion concentrations. It enhances cellular functions and metabolic activities by increasing the permeability of cell membranes to magnesium ions. Additionally, Magnesium ionophore III is utilized in research to explore the significance of magnesium ions in biological processes and their impact on cellular physiology.Formule :C30H58N4O4Couleur et forme :SolidMasse moléculaire :538.81LRAT-IN-1
CAS :LRAT-IN-1 (compound 1) is an inhibitor of lecithin retinol acyltransferase (LRAT) with an IC50 value of 21.1 μM. This compound works by inhibiting the esterification of retinol to form retinyl esters, thereby increasing the availability of retinol in the skin to deliver anti-aging benefits. LRAT-IN-1 is under investigation for its potential use as an anti-aging ingredient in cosmetics.Formule :C27H47N5O5S2Couleur et forme :SolidMasse moléculaire :585.82Monoamine Oxidase B inhibitor 6
CAS :Monoamine OxidaseB inhibitor 6 (Compound BT5) is a highly selective, reversible, and competitive MAO-B inhibitor capable of crossing the blood-brain barrier, with an IC50 of 0.11 μM. It exhibits antioxidant and neuroprotective properties, making it suitable for research into neurodegenerative diseases.Formule :C15H15N3OSCouleur et forme :SolidMasse moléculaire :285.364ACLY Inhibitor 7
CAS :ACLY Inhibitor 7 is a potent, selective hACLY inhibitor (IC50<1 nM) for metabolic disease and oncology research.Formule :C21H14ClF2NO6SDegré de pureté :99.74%Couleur et forme :SoildMasse moléculaire :481.852,4-Dihydroxybutanoic acid
CAS :2,4-Dihydroxybutanoic acid is typically not found in extracts of normal human urine and is present only in trace amounts in newborns, while cases of succinic semialdehyde dehydrogenase deficiency consistently exhibit elevated levels of this metabolite.Formule :C4H8O4Couleur et forme :SolidMasse moléculaire :120.104-Hydroxyclonidine
CAS :4-Hydroxyclonidine is a metabolite of Clonidine. It is equally effective as Clonidine in displacing labeled Clonidine from antibodies.Formule :C9H9Cl2N3OCouleur et forme :SolidMasse moléculaire :246.093Resolvin E2
CAS :RvE2, a bioactive lipid from the SPM family, is made from EPA and reduces inflammatory neutrophil infiltration and helps treat NAFLD and other diseases.Formule :C20H30O4Couleur et forme :SolidMasse moléculaire :334.45ONL-1204
CAS :ONL-1204 is a small molecule, CD95 antigen inhibitor (Fas inhibitor) being developed by ONL Therapeutics for the treatment of retinal detachment.Formule :C71H100N18O16Couleur et forme :SolidMasse moléculaire :1461.66Lapaquistat
CAS :Lapaquistat: active TAK-475 metabolite; reduces cholesterol synthesis and statin myotoxicity.Formule :C31H39ClN2O8Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :603.1FXIa-IN-10
FXIa-IN-10 is a potent, orally bioavailable inhibitor of Activator XI (FXIa) (Ki: 0.17 nM).Formule :C23H18Cl2F3N9O2Couleur et forme :SolidMasse moléculaire :580.35LXRβ agonist-2
CAS :LXRβ agonist-2 is a highly potent and β-selective liver X receptor (LXRβ) agonist with EC50 of 7 nM.Formule :C32H31F6N3O7Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :683.59Dimidazon
CAS :Dimidazon (BAS 29095) is a mild electron transport inhibitor that targets photosystem II (PSII). It blocks the electron flow from the primary electron acceptor Q to photosystem I within PSII. Dimidazon holds potential for research in photosynthesis regulation and weed control.Formule :C12H12N2O3Couleur et forme :SolidMasse moléculaire :232.24HSD17B13-IN-44
CAS :HSD17B13-IN-44 (Compound 23) functions as an inhibitor targeting hydroxysteroid 17β-dehydrogenase 13 (HSD17B13), exhibiting an IC50 value of < 0.1 μM against estradiol. This compound is applicable in the study of liver diseases or metabolic disorders [1].Formule :C18H14FNO5S2Masse moléculaire :407.44AZ513
CAS :AZ513 is a reversible FAAH inhibitor, exhibiting an IC50 of 551 nM for human FAAH and 27 nM for rat FAAH. It inhibits the hydrolysis of arachidonoyl ethanolamide in HEK293 cells transfected with human FAAH, with an IC50 of 360 nM.Formule :C14H9Cl2N3OCouleur et forme :SolidMasse moléculaire :306.147JTT-553
CAS :JTT-553 is a DGAT1 inhibitor with an IC50 of 2.38 nM. It effectively reduces plasma levels of glucose, insulin, non-esterified fatty acids (NEFA), total cholesterol (TC), and liver triglycerides (TG). JTT-553 enhances insulin-dependent glucose absorption and glucose intolerance in the adipose tissue of diet-induced obese (DIO) mice. In KK-Ay mice, it lowers TNF-α mRNA levels and elevates GLUT4 mRNA levels in adipose tissue. By contributing to weight loss, JTT-553 improves insulin resistance in adipose tissue and overall glucose metabolism. This compound is useful for research on obesity and type 2 diabetes mellitus (T2DM).Formule :C25H27F3N4O3Couleur et forme :SolidMasse moléculaire :488.50
