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(270 products)
- FAAH(64 products)
- FXR(58 products)
- Factor Xa(80 products)
- Fatty Acid Synthase(33 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(125 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)
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Found 8625 products of "Metabolism"
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SHP2-IN-37
<p>SHP2-IN-37 (compound C5) is a potent allosteric inhibitor selective for SHP2, with an IC50 of 0.023 μM. It exhibits antiproliferative effects on KYSE-520 and MV-411 cells, with IC50 values of 6.97 μM and 0.67 μM, respectively.</p>Formula:C19H22Cl2N4O2SColor and Shape:SolidMolecular weight:440.08405Lead Ionophore IV
CAS:<p>Lead Ionophore IV, an ion carrier, actively facilitates the transport of metal ions. It is commonly utilized in biological research to investigate the biological effects of lead ions and their impact on cellular functions. Additionally, Lead Ionophore IV is employed in developing drug delivery systems to enhance the bioavailability of compounds.</p>Formula:C60H84N4O4S4Color and Shape:SolidMolecular weight:1053.59O-Desethyl Sildenafil
CAS:<p>O-Desethyl sildenafil is a metabolite of the phosphodiesterase 5 (PDE5) inhibitor sildenafil .1</p>Formula:C20H26N6O4SColor and Shape:SolidMolecular weight:446.53Fmoc-Asp-OAll
CAS:<p>Fmoc-Asp-OAll (Fmoc-L-aspartic acid a-allyl ester) is an aspartic acid derivative.</p>Formula:C22H21NO6Purity:98.31%Color and Shape:SolidMolecular weight:395.4120,26-Dihydroxyecdysone
CAS:<p>20,26-Dihydroxyecdysone is a predominant ecdysteroid metabolite [1] .</p>Formula:C27H44O8Color and Shape:SolidMolecular weight:496.63Nicotinic Acid Adenine Dinucleotide
CAS:<p>Nicotinic Acid Adenine Dinucleotide is a precursor of NAD (Nicotinamide adenine dinucleotide) and a substrate for glutamine-dependent NAD+ synthase</p>Formula:C21H26N6O15P2Color and Shape:SoildMolecular weight:664.41(Ile8)-Oxytocin acetate
<p>(Ile8)-Oxytocin acetate is a neurohypophysial hormone analog of oxytocin produced in marsupials.</p>Formula:C45H70N12O14S2Color and Shape:SolidMolecular weight:1067.245-hydroxy Omeprazole
CAS:<p>5-hydroxy omeprazole, major omeprazole metabolite, formed by CYP2C19, affects gastric H+/K+ pump inhibition.</p>Formula:C17H19N3O4SColor and Shape:SolidMolecular weight:361.42D,L-erythro-PDMP
CAS:<p>D,L-erythro-PDMP inhibits growth in rabbit fibroblasts and blocks UDP-glucose: ceramide glucosyltransferase.</p>Formula:C23H38N2O3Color and Shape:SolidMolecular weight:390.568Inulobiose
CAS:<p>Inulobiose, a difructan disaccharide isolated from Pistacia vera L., demonstrates inhibitory effects on α-glycosidase (α-glycosidase) and α-amylase (α-amylase) activities, with IC50 values of 1.87 and 40.72 mg/mL respectively. It is utilized in research related to diabetes and glomerular filtration rate testing.</p>Formula:C12H22O11Color and Shape:SolidMolecular weight:342.3Linoleoyl-L-carnitine (chloride)
CAS:<p>Linoleoyl-L-carnitine, a natural acylcarnitine, rises in mouse liver post high-dose isoniazid (200 mg/kg).</p>Formula:C25H46ClNO4Color and Shape:SolidMolecular weight:460.12,3-Indolobetulin
CAS:<p>2,3-Indolobetulin is a pentacyclic triterpenoid and derivative of betulin .1It has been used in the synthesis of α-glucosidase inhibitors.</p>Formula:C36H51NOColor and Shape:SolidMolecular weight:513.81Ethyl gentisate
CAS:<p>Ethyl gentisate acts as a dual regulator of cell differentiation, promoting osteoblast differentiation while inhibiting osteoclast differentiation.</p>Formula:C9H10O4Purity:99.55%Color and Shape:SolidMolecular weight:182.17PKM2-IN-10
<p>PKM2-IN-10 is a PKM2 inhibitor. It effectively suppresses the proliferation of A549 and HCC1833 cell lines with IC50 values of 3.36 μM and 9.20 μM, respectively. PKM2-IN-10 demonstrates antitumor activity in human non-small cell lung cancer (NSCLC) and mouse lung adenocarcinoma models. It is applicable for research in lung cancer.</p>Formula:C21H15F4N5Color and Shape:SolidMolecular weight:413.12636H-Met-Val-OH
CAS:<p>H-Met-Val-OH is a dipeptide inhibiting FMO1 and FMO3 and promoting neurite outgrowth, relevant for neuroregenerative and enzymatic modulation studies.</p>Formula:C10H20N2O3SColor and Shape:SolidMolecular weight:248.34LY 295427
CAS:<p>LY 295427 is a bioactive chemical.</p>Formula:C30H52OColor and Shape:SolidMolecular weight:428.73ML266
CAS:<p>ML266: GCase chaperone, non-inhibiting, IC50=2.5 µM, aids mutant protein transport, may help in Gaucher disease study.</p>Formula:C24H22BrN3O4Purity:99.58%Color and Shape:SolidMolecular weight:496.35Ledelabricin alfa
<p>Ledelabricin alfa, an isoform A variant of human proteoglycan 4 (PRG4), functions as a lubricant for joints and boundaries.</p>Purity:98%Color and Shape:Odour LiquidPROTAC CYP1B1 degrader-1
CAS:<p>Compound 6C, a PROTAC degrader, targets CYP1B1 with IC50s (95.1 nM CYP1B1, 9838.6 nM CYP1A2) for prostate cancer research.</p>Formula:C43H39N5O10Color and Shape:SolidMolecular weight:785.8TC HSD 21
CAS:<p>TC HSD 21 is a potent and highly selective inhibitor of 17β-hydroxysteroid dehydrogenase type 3 (IC50 = 14 nM).</p>Formula:C17H12BrNO3S2Purity:98.5%Color and Shape:SolidMolecular weight:422.32
