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(271 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(98 products)
- Lipid(58 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(165 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 8628 products of "Metabolism"
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Dirlotapide
CAS:Dirlotapide (CP742033), an intestinal MTP inhibitor, cuts weight in diabetic dogs by lowering food intake and raising peptide YY.Formula:C40H33F3N4O3Purity:98.47% - 99.62%Color and Shape:SolidMolecular weight:674.71AGN 196996
CAS:<p>AGN 196996: strong RARα inhibitor (Ki: 2 nM), weak for RARβ/γ (Ki: 1087/8523 nM).</p>Formula:C24H20BrNO5Purity:98.74%Color and Shape:SolidMolecular weight:482.32BPDA2
CAS:BPDA2 selectively inhibits SHP2 (IC50=92nM) over SHP1/1B (33.39/40.71μM), curbs RTKs, and hampers SHP2-driven breast cancer cell traits.Formula:C24H30O5Purity:99.80%Color and Shape:SolidMolecular weight:398.49TDO-IN-1
CAS:<p>TDO-IN-1 is a tryptophan 2,3-dioxygenase (TDO) inhibitor with antitumor activity that acts by reversing local immune tolerance in tumor tissues.</p>Formula:C16H13F3N4O2Purity:99.86%Color and Shape:SolidMolecular weight:350.3CM037
CAS:<p>CM037 (A-37) is a selective ALDH1A1 (acetaldehyde dehydrogenase 1A1) inhibitor (IC50; 4.6 µM) with antitumor activity and may be used in studies to eliminate</p>Formula:C21H25N3O3S2Purity:99.34%Color and Shape:SolidMolecular weight:431.57CYP1B1-IN-4
CAS:<p>CYP1B1-IN-4: 2,4-diarylthiazole, selective CYP1B1 inhibitor (IC50=0.2 nM), low cytotoxicity, stable in liver microsomes.</p>Formula:C18H14N2O2SPurity:98.74%Color and Shape:SolidMolecular weight:322.38Atibeprone
CAS:Atibeprone is a MAO-B inhibitor with antidepressant activity for the study of Parkinson's disease.Formula:C17H18N2O3SPurity:99.18% - 99.86%Color and Shape:SolidMolecular weight:330.4PHGDH-IN-3
CAS:<p>PHGDH-IN-3, an oral PHGDH blocker with 2.8 μM IC50, may help in cancer research.</p>Formula:C24H18FN3O4S2Purity:97.24% - 98.55%Color and Shape:SolidMolecular weight:495.55EWP 815
CAS:<p>EWP 815, a disulfiram analog, inhibits Ins(1,4)P2, Ins(1,4,5)P3 phosphatases, and dopamine β-hydroxylase.</p>Formula:C12H22N4S4Purity:98%Color and Shape:SolidMolecular weight:350.59MK-0873
CAS:<p>MK-0873 is a novel and potent selective phosphodiesterase 4 (PDE4) inhibitor.</p>Formula:C25H18N4O3Purity:98.40%Color and Shape:SolidMolecular weight:422.44Isolithocholic Acid
CAS:<p>Isolithocholic Acid, a bile acid isomer, forms through microbial metabolism of Lithocholic acid or its 3α-sulfate.</p>Formula:C24H40O3Purity:99.56% - 99.84%Color and Shape:SolidMolecular weight:376.57HSD-016
CAS:HSD-016: Oral 11β-HSD1 inhibitor, active in humans, mice, rats (IC50: 11, 1, 8 nM), potential for type 2 diabetes research.Formula:C21H21F7N2O3SPurity:99.40% - >99.99%Color and Shape:SolidMolecular weight:514.46MAO-B-IN-8
CAS:<p>MAO-B-IN-8 is a highly potent and reversible inhibitor of monoamine oxidase-B (MAO-B), which also exhibits inhibitory effects on the microglial production of</p>Formula:C18H16O6Purity:99.62%Color and Shape:SolidMolecular weight:328.32BMS 753
CAS:<p>BMS 753 is an agonist of isotype-selective retinoic acid receptor α (RARα, Ki= 2 nM).</p>Formula:C21H21NO4Purity:98.55%Color and Shape:SolidMolecular weight:351.4MM-433593
CAS:<p>MM-433593 is a selective fatty acid amide hydrolase (FAAH-1) inhibitor for the treatment of pain, inflammation, and other disorders.</p>Formula:C25H22ClN3O3Purity:>99.99%Color and Shape:SolidMolecular weight:447.91MY10
CAS:<p>MY10, a potent and orally active inhibitor of the receptor protein tyrosine phosphatase (RPTPβ/ζ), effectively reduces binge-like ethanol consumption and</p>Formula:C15H10F6OS2Purity:98.64%Color and Shape:SolidMolecular weight:384.36K-111
CAS:<p>K-111 is a PPAR alpha agonist. K-111 improves insulin resistance, reducing bodyweight, and ameliorating atherogenic dyslipidemia.</p>Formula:C18H25Cl3O2Purity:99.64% - 99.88%Color and Shape:SolidMolecular weight:379.75Giripladib
CAS:<p>Giripladib (PLA695/PLX-695) blocks radiation-boosted phosphorylation of ERK and Akt in endothelial cells.</p>Formula:C41H36ClF3N2O4SPurity:99.64%Color and Shape:SolidMolecular weight:745.25MFI8
CAS:MFI8 is a compound that regulates mitochondrial fission and can be used to study aging.Formula:C16H18ClNOPurity:99.08% - 99.78%Color and Shape:SolidMolecular weight:275.77Ch55
CAS:<p>Ch55, a potent HL60 cell differentiator (EC50=200nM), binds well to RAR-α/β, useful for cancer research.</p>Formula:C24H28O3Purity:99.55%Color and Shape:SolidMolecular weight:364.48AMG-1694
CAS:<p>AMG-1694 disrupts GK-GKRP complex, enhancing GK activity with 7 nM IC50; normalizes glucose in diabetic rodents without affecting normoglycemic animals.</p>Formula:C23H30F3N3O4S2Purity:98.37%Color and Shape:SolidMolecular weight:533.63IGP-1
CAS:<p>iGP-1 is a cell-permeable mitochondrial sn-Glycerol 3-phosphate dehydrogenase (mGPDH) inhibitor.</p>Formula:C17H15N3O3Purity:99.12% - 99.15%Color and Shape:SolidMolecular weight:309.3211-cis-Vaccenyl acetate
CAS:<p>11-cis-Vaccenyl acetate ((Z)-Octadec-11-enyl acetate) activates olfactory neurons located in the T1 sensilla on the antenna and mediates aggregation behavior in</p>Formula:C20H38O2Purity:96.53% - 99.95%Color and Shape:LiquidMolecular weight:310.51Aleplasinin
CAS:<p>Aleplasinin (PAZ 417) is a selective and orally active inhibitor of Plasminogen activator inhibitor-1(PAI-1) and a key negative regulator of the fibrinolytic</p>Formula:C28H27NO3Purity:99.21%Color and Shape:SolidMolecular weight:425.52JNJ-40355003
CAS:<p>JNJ-40355003 is a FAAH inhibitor that increases plasma levels of fatty acid amides in rats, dogs, and crabs.</p>Formula:C23H23ClN4O2Purity:99.32%Color and Shape:SolidMolecular weight:422.91Chloramphenicol succinate
CAS:<p>Chloramphenicol succinate is a bacteriostatic antibiotic. CPSA is a competitive substrate and inhibitor of succinate dehydrogenase (SDH),can be oxidized by.</p>Formula:C15H16Cl2N2O8Purity:95.32%Color and Shape:Physical Description White Powder (Ntp 1992)Molecular weight:423.2Carbazeran
CAS:<p>Carbazeran (UK-31,557) is an inhibitor of PDE2 and PDE3 and can be used for studies about metabolic diseases.</p>Formula:C18H24N4O4Purity:99.3%Color and Shape:SolidMolecular weight:360.41AC-261066
CAS:<p>AC-261066 is an orally available and isoform-selective agonist of RARβ2 with a pEC50 of 8.0.</p>Formula:C17H20FNO4SPurity:99.64%Color and Shape:SolidMolecular weight:353.41PF-04447943
CAS:<p>PF-04447943, a selective PDE9A inhibitor (IC50=12nM), may aid sickle cell anemia research with its anti-inflammatory properties.</p>Formula:C20H25N7O2Purity:99.36% - 99.59%Color and Shape:SolidMolecular weight:395.46Rbin-2
CAS:Rbin-2: Potent, selective Midasin inhibitor; reversible, cell-permeable; halts eukaryotic ribosome assembly.Formula:C13H11BrN4SPurity:98.65%Color and Shape:SolidMolecular weight:335.22Edoxaban
CAS:<p>Edoxaban: potent, selective FXa inhibitor; Ki 0.561 nM. Used as an oral anticoagulant for stroke prevention, also inhibits thrombin and FIXa.</p>Formula:C24H30ClN7O4SPurity:97.67% - 99.71%Color and Shape:SolidMolecular weight:548.06Fenoverine
CAS:<p>Fenoverine (Spasmopriv) has antispasmodic activity and can be used to study gastrointestinal spasms.</p>Formula:C26H25N3O3SPurity:98.34%Color and Shape:SolidMolecular weight:459.56BRD7389
CAS:<p>BRD7389 is an inhibitor of RSK family kinase with IC50s of 1.5 μM, 2.4 μM, and 1.2 μM for RSK1, RSK2, and RSK3, respectively.</p>Formula:C24H18N2O2Purity:99.51%Color and Shape:SolidMolecular weight:366.41Ladostigil
CAS:<p>Ladostigil is an oral cholinesterase & MAO-B inhibitor used for depression and Alzheimer's studies.</p>Formula:C16H20N2O2Purity:97.48%Color and Shape:SolidMolecular weight:272.34GSK205
CAS:GSK205 is a selective TRPV4 antagonist (IC50: 4.19 μM) for inhibiting TRPV4-mediated Ca2+ influx.Formula:C24H25BrN4SPurity:99.46%Color and Shape:SolidMolecular weight:481.45Pradefovir
CAS:<p>Pradefovir (Remofovir) is a prodrug for chronic HBV, converting to PMEA in the liver with a Km of 60 μM and clearance of 359 ml/min.</p>Formula:C17H19ClN5O4PPurity:97.50%Color and Shape:SolidMolecular weight:423.79AICAR monophosphate
CAS:<p>AICAR monophosphate (Aica ribonucleotide) is a purine precursor with antineoplastic activity and can be used in studies about type 2 diabetes.</p>Formula:C9H15N4O8PPurity:99.8%Color and Shape:SolidMolecular weight:338.21IMPDH2-IN-2
CAS:<p>IMPDH2-IN-2 is an IMPDH inhibitor with antimicrobial activity and potential anti-tuberculosis activity for the study of inflammation and immune dysfunction.</p>Formula:C21H15Cl2N3O3Purity:99.02%Color and Shape:SolidMolecular weight:428.27ARRY-403
CAS:<p>ARRY-403 is a novel glucokinase activator that reduces fasting and postprandial blood glucose in patients with type 2 diabetes.</p>Formula:C20H18N6O3S2Purity:98.80%Color and Shape:SolidMolecular weight:454.52CYP1B1-IN-5
CAS:<p>CYP1B1-IN-5: selective CYP1B1 inhibitor, IC50 = 4.7 nM, useful for metabolism disease research.</p>Formula:C14H8INO2Purity:98.61%Color and Shape:SolidMolecular weight:349.12Nampt activator-2
CAS:<p>Nampt activator-2: Potent NAMPT activator (EC50: 0.023 μM), binds CYP2C9 (0.060 μM), 2D6 (0.41 μM), 2C19 (0.59 μM); useful in metabolic disease research.</p>Formula:C17H15ClN4O3SPurity:98.30% - 98.33%Color and Shape:SolidMolecular weight:390.84Tiapamil hydrochloride
CAS:<p>Tiapamil hydrochloride (Ro 11-1781 hydrochloride) is a calcium channel blocker with antihypertensive activity used in the study of angina pectoris.</p>Formula:C26H38ClNO8S2Purity:99.17%Color and Shape:SolidMolecular weight:592.16ALDH1A3-IN-2
CAS:<p>ALDH1A3-IN-2 is a potent ALDH1A3 inhibitor with an IC50 of 0.30 μM.ALDH1A3-IN-2 has potential for cancer disease research.</p>Formula:C13H17NOPurity:99.84%Color and Shape:SolidMolecular weight:203.28Phosphatase-IN-1
CAS:<p>Phosphatase-IN-1 is a phosphatidic acid phosphatase (Pah) inhibitor with antifungal activity for the study of rice blast and ruderalia.</p>Formula:C16H16Cl2FNO2Purity:99.88%Color and Shape:SolidMolecular weight:344.21SBI-425
CAS:<p>SBI-425: orally available TNAP inhibitor, enhances cardiovascular health & survival, no bone impact.</p>Formula:C13H12ClN3O4SPurity:99.88%Color and Shape:SolidMolecular weight:341.77JNJ-42226314
CAS:<p>JNJ-42226314 is a MAGL inhibitor with anti-injury effects and has shown efficacy in neuropathic pain and inflammatory pain models.</p>Formula:C26H24FN5O2SPurity:99.62%Color and Shape:SolidMolecular weight:489.56alphaSYN-IN-NAB2
CAS:<p>alphaSYN-IN-NAB2: a NAB2 gene protein guarding neurons against alpha-SYN harm; aids endosomal transport, cell processes, and can study various diseases.</p>Formula:C23H20ClN3OPurity:98.49%Color and Shape:SolidMolecular weight:389.88Izonsteride
CAS:<p>Izonsteride (LY320236) is a selective and potent 5alpha reductase inhibitor with dual action on the type I and type II isoforms of the enzyme.Izonsteride is</p>Formula:C24H26N2OS2Purity:99.55%Color and Shape:SolidMolecular weight:422.61HTS07545
CAS:<p>HTS07545, an SQOR inhibitor (IC50: 30nM), slows H2S breakdown, researched for heart failure.</p>Formula:C22H18N2O3Purity:99.71%Color and Shape:SolidMolecular weight:358.39Verofylline
CAS:<p>Verofylline (Verofyllinum) is an orally available, long-acting, multiacting, methylxanthine-substituted bronchodilator with inhibitory effects on PDE4 for the</p>Formula:C12H18N4O2Purity:98.33% - 98.83%Color and Shape:SolidMolecular weight:250.3
