
Metabolismo
Los inhibidores del metabolismo son compuestos que interfieren con las vías metabólicas, alterando la producción y utilización de energía dentro de las células. Estos inhibidores se utilizan para estudiar la regulación del metabolismo, el papel de las vías metabólicas en enfermedades como el cáncer y la diabetes, y para desarrollar nuevas estrategias terapéuticas. Los inhibidores del metabolismo pueden dirigirse a diversas enzimas y procesos involucrados en la glucólisis, la oxidación de ácidos grasos y otras funciones metabólicas. En CymitQuimica, ofrecemos una amplia gama de inhibidores del metabolismo de alta calidad para apoyar su investigación en bioquímica, trastornos metabólicos y desarrollo de fármacos.
Subcategorías de "Metabolismo"
- AhR(41 productos)
- Aminopeptidasa(67 productos)
- CETP(18 productos)
- Anhídrido carbónico(177 productos)
- Caseína quinasa(130 productos)
- DHFR(32 productos)
- Descarboxilasa(4 productos)
- Deshidrogenasa(267 productos)
- FAAH(63 productos)
- FXR(58 productos)
- Factor Xa(80 productos)
- Ácido graso sintasa(32 productos)
- Ferroptosis(215 productos)
- GR(3 productos)
- GSNOR(3 productos)
- Glucoquinasa(53 productos)
- HIF / HIF Prolilhidroxilasa(142 productos)
- HMG-CoA reductasa(32 productos)
- Hidroxilasa(30 productos)
- IDO(82 productos)
- LDL(8 productos)
- Lipasa(96 productos)
- Lípido(59 productos)
- Lipoxigenasa(124 productos)
- MAO(87 productos)
- MPO(2 productos)
- NAMPT(36 productos)
- P450(6 productos)
- PAI-1(25 productos)
- PDE(165 productos)
- PED(1 productos)
- PKM(15 productos)
- PPAR(164 productos)
- Fosfolipasa(82 productos)
- ROR(42 productos)
- Receptor de retinoides(29 productos)
- SGK(11 productos)
- Tiorredoxina(12 productos)
- Transferasa(30 productos)
- Transportador(42 productos)
- UGT(4 productos)
- Inhibidores de la xantina oxidasa (XO)(9 productos)
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Se han encontrado 8597 productos de "Metabolismo"
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Arachidonoyl-N-methyl amide
CAS:<p>Anandamide (AEA), an endogenous cannabinoid, interacts with both central (CB1) and peripheral (CB2) cannabinoid receptors. Its effects are concluded through the cellular uptake and enzymatic breakdown of its amide bond by fatty acid amide hydrolase. Arachidonoyl-N-methyl amide, an analog of anandamide, specifically targets the human CB1 receptor, displaying a binding affinity with a Ki of 60 nM. It completely inhibits rat glial gap junction intercellular communication at a concentration of 50 µM.</p>Fórmula:C21H35NOForma y color:SolidPeso molecular:317.5cis-8-Octadecenoic Acid
CAS:<p>Cis-8-Octadecenoic acid, a monounsaturated fatty acid and isomer of oleic acid, trans-vaccenic acid, trans-petroselinic acid, and cis-petroselinic acid, is present in partially hydrogenated vegetable oil and milk fat.</p>Fórmula:C18H34O2Forma y color:SolidPeso molecular:282.46GIV3727
CAS:<p>GIV3727, a bitter taste receptor hTAS2R antagonist, inhibits the activation of hTAS2R31 by saccharin and acesulfame potassium, effectively diminishing the</p>Fórmula:C12H22O2Forma y color:SolidPeso molecular:198.3(R)-IDO/TDO-IN-1
CAS:<p>(R)-IDO/TDO-IN-1 (compound 25), an indoleamine-2,3-dioxygenase (IDO) inhibitor, demonstrates good pharmacokinetic properties and exerts anti-tumor effects in the MC38 xenograft model. This compound exhibits synergy when combined with the anti-PD-1 monoclonal antibody (SHR-1210) [1].</p>Fórmula:C25H24FN5Forma y color:SolidPeso molecular:413.49Biliverdin
CAS:<p>Biliverdin, produced through the oxidation of bilirubin, can also be synthesized through a non-protoporphyrin pathway in Corynebacterium glutamicum [1].</p>Fórmula:C33H34N4O6Forma y color:SolidPeso molecular:582.65ICMT-IN-21
CAS:<p>ICMT-IN-21 (compound 6ag) is an ICMT inhibitor with an IC50 value of 8.8 µM, featuring sulfonamide-modified farnesyl cysteine (SMFC).</p>Fórmula:C22H33NO4S3Forma y color:SolidPeso molecular:471.7Clocortolone pivalate
CAS:<p>Clocortolone pivalate, a synthetic steroid, treats dermatitis and psoriasis.</p>Fórmula:C27H36ClFO5Forma y color:SolidPeso molecular:495.02LB-60-OF61
CAS:<p>LB-60-OF61 is a NAMPT inhibitor, a NAMPT inhibitor that displays antiproliferative activity against MYC oncogene-dependent cancer cell lines.</p>Fórmula:C29H30N6O2Pureza:99.47%Forma y color:SolidPeso molecular:494.59ML395
CAS:<p>ML395 is a potent, selective PLD2 allosteric inhibitor with potent antiviral activity (IC50 =360 nM).</p>Fórmula:C26H29N5O2Pureza:98%Forma y color:SolidPeso molecular:443.54Amb123203
CAS:<p>Amb123203 is an inhibitor of the budding of mVP40 and eVP40 VLPs that acts by blocking mVP40-795 Nedd4 protein-protein interaction.</p>Fórmula:C25H27N5OSForma y color:SolidPeso molecular:445.58FXa-IN-1
CAS:<p>FXa-IN-1, an FXa blocker: IC50=3 nM, Ki=0.7 nM, orally available, long half-life, for thrombosis research.</p>Fórmula:C24H18F5N5OForma y color:SolidPeso molecular:487.42DPM-1001 trihydrochloride
<p>DPM-1001 trihydrochloride: Potent PTP1B inhibitor, IC50 100 nM, oral, non-competitive, anti-diabetic.</p>Fórmula:C35H60Cl3N3O3Forma y color:SolidPeso molecular:677.23α-Glucosidase-IN-11
CAS:<p>α-Glucosidase-IN-11 is a highly permeable competitive inhibitor of α-glucosidase (IC50: 0.56 μM).</p>Fórmula:C23H20N2O6Forma y color:SolidPeso molecular:420.41H-0104 Dihydrochloride
CAS:<p>H-0104 Dihydrochloride is an inhibitor of ROCK that acts by applying potent intraocular pressure (IOP)-lowering effects into the eyes of monkeys.</p>Fórmula:C15H20BrCl2N3O2SPureza:98%Forma y color:SolidPeso molecular:457.21Bemfivastatin hemicalcium
CAS:<p>Bemfivastatin hemicalcium (PPD 10558), an orally active HMG-CoA reductase inhibitor, serves as a lipid-lowering agent.</p>Fórmula:C34H36FN2O6CaForma y color:SolidPeso molecular:607.67sPLA2 inhibitor 1
CAS:<p>KH064 is a sPLA2-IIA inhibitor of oral activity.</p>Fórmula:C31H37NO4Forma y color:SolidPeso molecular:487.63M5N36
CAS:<p>M5N36: selective Cdc25C inhibitor, IC50: 0.15µM A, 0.19µM B, 0.06µM C; halts cell growth, boosts p-CDK1/2.</p>Fórmula:C20H16ClN5O3Forma y color:SolidPeso molecular:409.83Iomazenil
CAS:<p>Iomazenil is an antagonist and partial inverse agonist of benzodiazepine and potential therapy for alcohol abuse.</p>Fórmula:C15H14IN3O3Pureza:98%Forma y color:SolidPeso molecular:411.19A 62198
CAS:<p>A 62198 is a potent and selective renin inhibitor with potential as a hypotensive agent.</p>Fórmula:C30H44N8O5Pureza:98%Forma y color:SolidPeso molecular:596.72NUCC-0223619
CAS:<p>NUCC-0223619 is an IDO1 inhibitor that induces the degradation of IDO protein and can be involved in the synthesis of PROTAC.</p>Fórmula:C24H24ClFN2O2Forma y color:SolidPeso molecular:426.91
