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(197 products)
- Casein Kinase(139 products)
- DHFR(30 products)
- Decarboxylase(4 products)
- Dehydrogenase(302 products)
- FAAH(64 products)
- FXR(63 products)
- Factor Xa(87 products)
- Fatty Acid Synthase(37 products)
- Ferroptosis(233 products)
- GR(3 products)
- GSNOR(3 products)
- Glucokinase(56 products)
- HIF/HIF Prolyl-Hydroxylase(146 products)
- HMG-CoA Reductase(36 products)
- Hydroxylase(36 products)
- IDO(84 products)
- LDL(7 products)
- Lipase(107 products)
- Lipid(62 products)
- Lipoxygenase(134 products)
- MAO(84 products)
- MPO(2 products)
- NAMPT(40 products)
- P450(6 products)
- PAI-1(26 products)
- PDE(169 products)
- PED(1 products)
- PKM(17 products)
- PPAR(170 products)
- Phospholipase(84 products)
- ROR(47 products)
- Retinoid Receptor(17 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 9198 products of "Metabolism"
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(3S,5R)-Fluvastatin sodium
CAS:(3S,5R)-Fluvastatin sodium: synthetic HMG-CoA reductase inhibitor, IC50 8 nM, boosts vascular cell antioxidant defense.Formula:C24H26FNNaO4Purity:98%Color and Shape:SolidMolecular weight:434.463Pancreatic lipase/Carboxylesterase 1-IN-1
CAS:Compound 39 is a dual inhibitor of PL (IC50: 2.13 μM) and hCES1A (IC50: 0.055 μM).Formula:C30H44O4Color and Shape:SolidMolecular weight:468.67Afegostat D-Tartrate
CAS:Afegostat D-Tartrate: pharmacological chaperone, reversibly binds acid-β-glucosidase in ER with high affinity.Formula:C10H19NO9Purity:98%Color and Shape:SolidMolecular weight:297.26HIF-1α inhibitor-1
CAS:HIF-1α inhibitor-1 is a HIF-1 alpha inhibitor.Formula:C15H11N3O4Color and Shape:SolidMolecular weight:297.27Acarbose sulfate
CAS:Acarbose sulfate is an anti-diabetic drug and is an inhibitor of alpha-glucosidase.Formula:C25H45NO22SPurity:98%Color and Shape:SolidMolecular weight:743.68VP3.15
CAS:VP3.15 is an orally bioavailable and CNS-penetrant dual inhibitor of phosphodiesterase (PDE)7- GSK3 (IC50s: 1.59 μM and 0.88 μM for PDE7 and GSK-3).Formula:C20H22N4OSPurity:98%Color and Shape:SolidMolecular weight:366.48Indoleacetyl phenylalanine
CAS:Indoleacetyl phenylalanine is an indole-acetyl-amino acid involved in regulating auxin activity.Formula:C19H18N2O3Purity:98%Color and Shape:SolidMolecular weight:322.36ATX inhibitor 14
CAS:ATX inhibitor 14, an indole carbamate, potently blocks self-adhesive proteins (IC50: 0.41 nM), aiding fibrosis research.Formula:C26H26Cl2N4O3SColor and Shape:SolidMolecular weight:545.48L-(-)-threo-3-Hydroxyaspartic acid
CAS:L-(-)-threo-3-Hydroxyaspartic acid is an EAAT1-4 inhibitor/non-transportable EAAT5 inhibitor.Formula:C4H7NO5Purity:98%Color and Shape:SolidMolecular weight:149.1Sp-Cyclic AMPS (sodium salt)
CAS:Sp-cAMPS Na salt activates PKA I/II and competitively inhibits PDE3A (Ki: 47.6 μM), also binds PDE10 GAF (EC50: 40 μM).Formula:C10H12N5NaO5PSColor and Shape:SolidMolecular weight:367.25Quinalizarin
CAS:Quinalizarin, the most selective CK2 inhibitor, is superior to CX-4945 which is the first-in-class CK2 inhibitor.Formula:C14H8O6Purity:98%Color and Shape:SolidMolecular weight:272.21SHP836
CAS:SHP836 is an inhibitor of SHP2 allosteric (IC50: 12 μM for the full-length SHP2).Formula:C16H19Cl2N5Purity:98%Color and Shape:SolidMolecular weight:352.26ATX inhibitor 20
CAS:ATX inhibitor 20 is a potent inhibitor of ATX (IC50: 2.3 nM).Formula:C31H34FN5O3Color and Shape:SolidMolecular weight:543.63HZ52
CAS:HZ52: Potent reversible 5-LO inhibitor; IC50 0.7 μM; blocks LTs in human leukocytes.Formula:C24H26ClN3O2SColor and Shape:SolidMolecular weight:456NCX 1000
CAS:NCX 1000 is a liver-specific NO donor compound,NCX 1000 derived from ursodeoxycholic acid (UDCA).Formula:C38H55NO10Purity:98%Color and Shape:SolidMolecular weight:685.84Rosuvastatin lactone
CAS:Tilavonemab (ABBV-8E12) is a monoclonal antibody that binds to the N-terminus of the human microtubule-associated protein tau.Formula:C22H26FN3O5SColor and Shape:SolidMolecular weight:463.52L 669262
CAS:L 669262 is a potent inhibitor of HMG-CoA reductase.Formula:C25H36O6Color and Shape:SolidMolecular weight:432.55Abiraterone metabolite 1
CAS:Abiraterone metabolite 1, a derivative of abiraterone, inhibits CYP17A1, halts androgen formation, aiding in prostate cancer treatment.Formula:C24H33NOPurity:98%Color and Shape:SolidMolecular weight:351.52EP6
CAS:EP6 blocks 5-LO, key in the AA cascade, reducing leukotrienes to curb inflammation and allergies.Formula:C24H30N4OPurity:98%Color and Shape:SolidMolecular weight:390.52NEP-IN-2
CAS:NEP-IN-2 is an inhibitor of neutral endopeptidase. It also is used in the research of proliferation in atherosclerosis, restenosis.Formula:C16H23NO3S2Purity:98%Color and Shape:SolidMolecular weight:341.49MPO-IN-4
CAS:MPO-IN-4, a potent MPO inhibitor (IC50=25 nM), also inhibits TPO (IC50=2.2 μM), but not MGMT.Formula:C12H11N5Color and Shape:SolidMolecular weight:225.25RORγt/DHODH-IN-2
CAS:RORγt/DHODH-IN-2 (compound 1) is a potent dual RORγt/DHODH inhibitor that can be used in the study of inflammatory bowel disease (IBD).Formula:C25H30N4OSColor and Shape:SolidMolecular weight:434.6Glyoxalase I inhibitor 1
CAS:Glyoxalase I inhibitor 1 is a potent inhibitor of glyoxalase I (GLO1) (IC50: 26 nM).Formula:C30H27FN6O4SColor and Shape:SolidMolecular weight:586.64(+)-Cembrene A
CAS:(+)-Cembrene A, a nontoxic α-glucosidase inhibitor to human normal hepatocyte (LO2) cells, exhibits an IC50 value of 30.31 μM.Formula:C20H32Color and Shape:SolidMolecular weight:272.47BMS 961
CAS:BMS961 is a potent and selective retinoic acid receptor gamma (RARγ) agonist (IC50: 30 nM).Formula:C23H26FNO4Purity:98%Color and Shape:SolidMolecular weight:399.46LTV-1
CAS:LTV-1 has the potential for autoimmunity treatment. LTV-1 is a potent lymphoid tyrosine phosphatase (LYP) inhibitor in T cells with an IC50 of 508 nM.Formula:C26H20N2O5SColor and Shape:SolidMolecular weight:472.51Tibenelast sodium
CAS:Tibenelast sodium is an inhibitor of phosphodiesterase.Formula:C13H14NaO4SPurity:98%Color and Shape:SolidMolecular weight:289.3Pulixin
CAS:Pulixin blocks FREP1 from P. falciparum, hinders parasite spread (EC50: 11µM), and stops its growth (EC50: 47nM).Formula:C14H11NO4Color and Shape:SolidMolecular weight:257.24(RS)-Eflucimibe
CAS:Eflucimibe is an ACAT inhibitor.Formula:C29H43NO2SPurity:98%Color and Shape:SolidMolecular weight:469.72CDP 840 hydrochloride
CAS:CDP-840 (GR259653X), a potent oral PDE IV inhibitor, curbs early and late phase bronchoconstriction in squirrel monkeys.Formula:C25H27NO2Color and Shape:SolidMolecular weight:373.49TDP1 Inhibitor-2
CAS:TDP1 Inhibitor-2 strongly blocks TDP1 (IC50: 99 nM) & treats SCAN1 (IC50: 3.5 μM).Formula:C25H14Cl2O5Color and Shape:SolidMolecular weight:465.28Succinyladenosine
CAS:Succinyladenosine, a marker for ASL deficiency, is made by dephosphorylating S-AMP with 5-nucleotidase.Formula:C14H17N5O8Color and Shape:SolidMolecular weight:383.317SCH-351591
CAS:SCH-351591 is an orally active inhibitor of phosphodiesterase 4.Formula:C17H10Cl2F3N3O3Purity:98%Color and Shape:SolidMolecular weight:432.18AHR-15010
CAS:AHR-15010 is a novel anti-arthritic agent.Formula:C10H16N2O8S2Purity:98%Color and Shape:SolidMolecular weight:356.3793-O17O
CAS:93-O17O is a cationic lipidoid used in lipid nanoparticles for spleen-targeted delivery and genome editing in mice.Formula:C44H83N3O6Color and Shape:SolidMolecular weight:750.15M8891
CAS:M8891: Oral, reversible MetAP-2 inhibitor, brain-penetrant (IC50: 54nM; Ki: 4.33nM), hinders endothelial & tumor cell growth, antiangiogenic & antitumor.Formula:C20H17F2N3O3Color and Shape:SolidMolecular weight:385.36Oosponol
CAS:Oosponol is a dopamine beta-hydroxylase inhibitor exhibiting hypotensive effects.Formula:C11H8O5Purity:98%Color and Shape:SolidMolecular weight:220.18α-Glucosidase-IN-3
CAS:α-Glucosidase-IN-3 is an oleanolic acid oxime ester derivative targeting α-glucosidase and α-amylase with an IC50 value of 0.35 μM for α-glucosidase.Formula:C39H53NO4Color and Shape:SolidMolecular weight:599.84Win-62005
CAS:Win-62005 is an inhibitor of cyclic AMP phosphodiesterase III (PDE III)(Kis: 25 and 26 nM for rat heart and canine aorta).Formula:C12H10N4OPurity:98%Color and Shape:SolidMolecular weight:226.23BN-82685
CAS:BN-82685, a quinone-based CDC25 inhibitor, shows in vitro and in vivo efficacy, suggesting potential as an anticancer therapy.Formula:C12H15N3O2SPurity:98%Color and Shape:SolidMolecular weight:265.33Fenleuton
CAS:Fenleuton is a 5-lipoxygenase inhibitor.Formula:C17H15FN2O3Purity:98%Color and Shape:SolidMolecular weight:314.31GKA-22
CAS:GKA-22 is a human glucokinase allosteric activator in the absence of glucose.Formula:C22H22N2O5SPurity:98%Color and Shape:SolidMolecular weight:426.49HCAIX-IN-2
CAS:HCAIX-IN-2 (compound 9d) is a selective inhibitor of carbonic anhydrase and acts on hCA IX (Ki: 24.6 nM) and hCA XII (Ki: 45.3 nM).Formula:C19H16N8O4SColor and Shape:SolidMolecular weight:452.45Piragliatin
CAS:Piragliatin (RO4389620) activates glucokinase, boosts insulin, and lowers glucose in type 2 diabetes.Formula:C19H20ClN3O4SColor and Shape:SolidMolecular weight:421.9Seviteronel racemate
CAS:Seviteronel racemate is the racemate form of Seviteronel and is a potent inhibitor of CYP17 lyase.Formula:C18H17F4N3O3Purity:98%Color and Shape:SolidMolecular weight:399.34Darexaban glucuronide
CAS:Darexaban glucuronide is the major component in plasma after oral administration of darexaban to humans. Darexaban (YM150) is a direct inhibitor of factor Xa.Formula:C33H38N4O10Color and Shape:SolidMolecular weight:650.68Sterculic acid
CAS:Sterculic acid inhibits SCD1 with IC50 of 0.9μM, affecting Δ9D desaturase activity.Formula:C19H34O2Color and Shape:SolidMolecular weight:294.47ONO-1603
CAS:ONO-1603, a prolyl endopeptidase inhibitor, is used potentially for the treatment of Alzheimer's disease.Formula:C16H19ClN2O3Purity:98%Color and Shape:SolidMolecular weight:322.79Fodipir
CAS:Fodipir, the active metabolite of mangafodipir, plays a crucial role in the mechanism of mangafodipir-mediated cytoprotection, specifically mitigating cellFormula:C22H32N4O14P2Purity:98%Color and Shape:SolidMolecular weight:638.46Enpp-1-IN-6
CAS:Enpp-1-IN-6, a potent enpp-1 inhibitor, may aid cancer and infectious disease studies (WO2021203772A1, compound 51).Formula:C22H28N4O5SColor and Shape:SolidMolecular weight:460.55
