
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(177 products)
- Casein Kinase(130 products)
- DHFR(32 products)
- Decarboxylase(4 products)
- Dehydrogenase(267 products)
- FAAH(63 products)
- FXR(58 products)
- Factor Xa(80 products)
- Fatty Acid Synthase(32 products)
- Ferroptosis(215 products)
- GR(3 products)
- GSNOR(3 products)
- Glucokinase(53 products)
- HIF/HIF Prolyl-Hydroxylase(142 products)
- HMG-CoA Reductase(32 products)
- Hydroxylase(30 products)
- IDO(82 products)
- LDL(8 products)
- Lipase(96 products)
- Lipid(59 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(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)
Show 34 more subcategories
Found 8595 products of "Metabolism"
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Maltodextrin, dextrose equivalent 16.5-19.5
CAS:<p>Maltodextrin (DE 16.5-19.5) is an inactive pharma excipient that enhances drug stability, solubility, and processing.</p>Formula:(C6H10O5)n·xH2OColor and Shape:SolidARL67156 trisodium hydrate
<p>ARL67156 trisodium hydrate inhibits ecto-ATPase, NTPDase1, NTPDase3, NPP1 (Kis 11-18µM), for calcific valve disease, asthma research.</p>Formula:C15H23Br2N5Na3O13P3Color and Shape:SolidMolecular weight:834.61Casuarictin
CAS:<p>Casuarictin, a potent competitive inhibitor of α-glucosidase, exhibits an IC50 of 0.21 μg/mL and functions as a presenilin stabilization factor-like (PSFL)</p>Formula:C41H28O26Purity:98%Color and Shape:SolidMolecular weight:936.65Genz-123346
CAS:<p>Genz-123346 is an oral inhibitor of glucosylceramide synthase, blocking ceramide to GL1 conversion, with a 14 nM IC50.</p>Formula:C52H82N4O14Purity:98%Color and Shape:SolidMolecular weight:987.23ω-Conotoxin CVIA
CAS:<p>ω-Conotoxin CVIA, a 27-amino acid neuropeptide, functions as a blocker of voltage-sensitive calcium channels (VSCCs) [1].</p>Formula:C97H161N39O36S6Purity:98%Color and Shape:SolidMolecular weight:2641.95ω-Conotoxin MVIID
<p>ω-Conotoxin MVIID (SNX-238) is a peptide from the Conus genus that inhibits the ω-Conotoxin-GVIA-sensitive, high-threshold calcium (Ca 2+) current in fish</p>Formula:C99H164N42O33S7Purity:98%Color and Shape:SolidMolecular weight:2695.08Hepcidin-25 (human) (acetate)
CAS:<p>Hepcidin-25 (human) acetate is a modulator of iron metabolism that demonstrates anti-inflammatory and antibacterial effects through the modulation of iron-</p>Formula:C113H170N34O31S9·xC2H4O2Purity:98%Color and Shape:SolidLarsucosterol sodium
CAS:<p>Larsucosterol sodium: a liver-derived cholesterol byproduct; modulates lipid synthesis, inflammation, and cell death regulation.</p>Formula:C27H46NaO5SColor and Shape:SolidMolecular weight:505.71Ovotransferrin (328-332)
CAS:<p>Ovotransferrin (328-332), with an IC50 of 20 μM, exhibits protective activity against hypertension by inhibiting the Angiotensin-Converting Enzyme (ACE) and</p>Formula:C25H46N8O7Purity:98%Color and Shape:SolidMolecular weight:570.68DSM1465
<p>DSM1465 (Compound 82) is a potent and selective inhibitor of P. falciparum dihydroorotate dehydrogenase (PfDHODH) with an IC50 value of 15 nM. It inhibits P. falciparum 3D7 (Pf3D7) parasites with an EC50 value of 1.4 nM and demonstrates significant in vivo efficacy in humanized P. falciparum mouse models.</p>Formula:C17H12ClF6N5O2Color and Shape:SolidMolecular weight:467.753α-Glucosidase-IN-36
<p>α-Glucosidase-IN-36 (compound 5g) is a potent inhibitor of α-glucosidase, exhibiting an IC50 value of 6.69 ± 0.18 μM and inhibition constants Ki and Kis of 1.65</p>Formula:C26H24BrN5O3SPurity:98%Color and Shape:SolidMolecular weight:566.47Seco Rapamycin
CAS:<p>Seco Rapamycin, a ring-opened Rapamycin derivative, does not affect mTOR function.</p>Formula:C51H79NO13Color and Shape:SolidMolecular weight:914.187Myoregulin TFA
<p>Myoregulin (MLN peptide) TFA, belonging to the regulin family, is a regulator of muscle performance through modulation of intracellular calcium dynamics.</p>Formula:C239H391N53O67S3·xC2HF3O2Purity:98%Color and Shape:SolidMolecular weight:5175.17 (free base)VHL-IN-1
<p>VHL-IN-1 (compound 30), a ubiquitin E3 ligase von Hippel-Lindau (VHL) inhibitor with a dissociation constant (Kd) of 37 nM, potently stabilizes HIF-1α and</p>Formula:C28H37FN4O4SPurity:98%Color and Shape:SolidMolecular weight:544.68ER 50891 quarterhydrate
<p>ER 50891 quarterhydrate is a potent RARα (retinoic acid receptor α) antagonist that markedly diminishes the inhibitory effects of ATRA (all-trans retinoic acid</p>Formula:C29H24N2O2H2OColor and Shape:SolidMolecular weight:437.02IOX2-NH2-1
CAS:<p>IOX2-NH2-1 inhibits E. coli EGLN-3 (prolyl hydroxylase) with an IC50 of 0.02–1 μM.</p>Formula:C19H17N3O5Purity:98.77% - 99.91%Color and Shape:SoildMolecular weight:367.36Alternaphenol B2
<p>Alternaphenol B2, a selective inhibitor of mutant isocitrate dehydrogenase 1 (IDH1m), is sourced from the coral-derived fungus Parengyodontium album SCSIO</p>Purity:98%Color and Shape:Odour SolidAcremin F
CAS:<p>Acremin F is a useful organic compound for research related to life sciences. The catalog number is T124074 and the CAS number is 863480-61-9.</p>Formula:C12H20O4Color and Shape:SolidMolecular weight:228.288Xanthine oxidase-IN-11
<p>Xanthine Oxidase-IN-11, an analog of XO8, is an inhibitor of xanthine oxidase (XO) [1].</p>Formula:C10H8N2OSPurity:98%Color and Shape:SolidMolecular weight:204.25ω-Conotoxin Bu8
<p>ω-Conotoxin Bu8 is a 25-amino-acid-residue ω-conotoxin that features three disulfide bridges.</p>Formula:C103H174N42O35S6Purity:98%Color and Shape:SolidMolecular weight:2753.13

