
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 8626 products of "Metabolism"
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PR280
<p>PR280 is a potent inhibitor of dihydroceramide desaturase 1 (Des1) with an IC50 of 700 nM. It forms hydrogen bonds with amino acid residues of Des1, while its cyclopropenone group may coordinate with the iron center, stabilizing its binding at Des1's active site. This inhibits the ceramide biosynthesis pathway, preventing dihydroceramide (dhCer) from converting into ceramide. PR280 can be used in research related to sphingolipid metabolism disorders, including cancer and metabolic diseases.</p>Formula:C27H49NO4Molecular weight:451.36616WWL123
CAS:<p>WWL123 is a potent and selective ABHD6 inhibitor (IC50=430 nM).</p>Formula:C28H24N2O3Purity:99.62%Color and Shape:SolidMolecular weight:436.5hCAIX/XII-IN-7
<p>Compound 3e (hCAIX/XII-IN-7) is a potent inhibitor of human carbonic anhydrase (hCA) isozymes IX and XII, displaying inhibitory constants (Kis) of 503.7 nM for</p>Formula:C17H14N6O3SPurity:98%Color and Shape:SolidMolecular weight:382.4HIF-1α-IN-2 hydrochloride
<p>HIF-1α-IN-2 hydrochloride is a potent HIF-1α inhibitor exhibiting anticancer activity, demonstrated by IC50 values of 28 nM in MDA-MB-231 cells and 15 nM in</p>Formula:C21H20ClN3OSPurity:98%Color and Shape:SolidMolecular weight:397.92α-Glucosidase-IN-32
<p>α-Glucosidase-IN-32 (compound f26) is a reversible, noncompetitive inhibitor of α-glucosidase that is orally active and exhibits an IC50 of 3.07 μM.</p>Formula:C32H22N4OSPurity:98%Color and Shape:SolidMolecular weight:510.61HIF-1 α (556-574) (TFA)
<p>HIF-1 alpha (556-574) TFA is a 19-residue fragment of hypoxia-inducible factor-1 (HIF-1), which serves as the master regulator of oxygen homeostasis [1].</p>Purity:98%Color and Shape:Odour SolidMicroginin 527
CAS:<p>Microginin 527, a compound found in Microcystis, is an inhibitor of protein phosphatase, ACE, and leucine aminopeptidase.</p>Formula:C25H41N3O7SColor and Shape:SolidMolecular weight:527.67(25R)-12α-Hydroxyspirost-4-en-3-one
CAS:<p>'(25R)-12α-Hydroxyspirost-4-en-3-one is a minor metabolite resulting from Nocardia globerula's metabolization of Hecogenin [1].'</p>Formula:C27H40O4Color and Shape:SolidMolecular weight:428.6Nampt degrader-2
<p>Nampt degrader-2: a fluorescent PROTAC that degrades NAMPT at IC50 41.9 nM, reducing NAD+ and having anti-tumor effects.</p>Formula:C59H73N9O7SColor and Shape:SolidMolecular weight:1052.33cis-5-Tetradecenoic acid
CAS:<p>cis-5-Tetradecenoic acid, found in blood, helps study Long Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency.</p>Formula:C14H26O2Color and Shape:SolidMolecular weight:226.36Acrihellin
CAS:<p>Acrihellin is a cardioactive steroid, a cardiotonic drug.</p>Formula:C29H38O7Color and Shape:SolidMolecular weight:498.61Aspergillomarasmine A
CAS:<p>Aspergillomarasmine A is a polyamine acid naturally produced by the mold Aspergillus Versicolor.</p>Formula:C10H17N3O8Purity:98%Color and Shape:SolidMolecular weight:307.26N-Trifluoroacetyladriamycin
CAS:<p>N-Trifluoroacetyladriamycin, Valrubicin's metabolite, treats bladder cancer; it's an analog of doxorubicin, infused into the bladder.</p>Formula:C29H28F3NO12Color and Shape:SolidMolecular weight:639.533PDK-IN-2
<p>PDK-IN-2 (Compound 1F), with an IC50 of 68 nM, is a potent PDK inhibitor that downregulates the expression of PDK1 and PDK4 in cells.</p>Formula:C17H23AsCl2N2O2S2Color and Shape:SolidMolecular weight:497.33A32390A
CAS:<p>A32390A, an antibiotic inhibitor, shows antimicrobial activity against gram-positive bacteria and fungi.</p>Formula:C18H24N2O8Color and Shape:SolidMolecular weight:396.39Rennin
CAS:<p>Rennin or Chymosin, a stomach enzyme in some animals, curdles milk by cleaving K-casein; key in cheese making.</p>Color and Shape:Solidα-1,3-N-Acetylgalactosaminyltransferase (Pm1138)
CAS:<p>Alpha-1,3-N-Acetylgalactosaminyltransferase (Pm1138) (EC 2.4.1.40(Pm1138)), also known as the ABO system transferase, exhibits glycosyl transferase activity [1</p>Color and Shape:SolidLYP-IN-3
<p>LYP-IN-3 (compound D34) is a selective Lymphoid-tyrosine phosphatase (LYP) inhibitor (Ki=0.93 μM) that modulates the T-cell receptor (TCR) signaling pathway</p>Formula:C35H27NO6SPurity:98%Color and Shape:SolidMolecular weight:589.66Nattokinase
CAS:<p>Nattokinase is a serine protease derived from nattō, oral, fibrinolytic/anticoagulant properties. It degrades fibrin, fibrinolytic substrates, and PAI-1.</p>Color and Shape:Solidω-Conotoxin CVIF
<p>ω-Conotoxin CVIF is a selective inhibitor of Ca v 2.2 channels, demonstrating an IC50 value of 34.3 nM in isolated rat DRG neurons.</p>Formula:C101H170N40O33S6Purity:98%Color and Shape:SolidMolecular weight:2665.07

