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(178 productos)
- Caseína quinasa(130 productos)
- DHFR(33 productos)
- Descarboxilasa(4 productos)
- Deshidrogenasa(271 productos)
- FAAH(64 productos)
- FXR(58 productos)
- Factor Xa(80 productos)
- Ácido graso sintasa(33 productos)
- Ferroptosis(215 productos)
- GR(3 productos)
- GSNOR(3 productos)
- Glucoquinasa(54 productos)
- HIF / HIF Prolilhidroxilasa(142 productos)
- HMG-CoA reductasa(33 productos)
- Hidroxilasa(30 productos)
- IDO(82 productos)
- LDL(8 productos)
- Lipasa(98 productos)
- Lípido(58 productos)
- Lipoxigenasa(124 productos)
- MAO(87 productos)
- MPO(2 productos)
- NAMPT(36 productos)
- P450(6 productos)
- PAI-1(25 productos)
- PDE(166 productos)
- PED(1 productos)
- PKM(15 productos)
- PPAR(165 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 8628 productos de "Metabolismo"
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Diproteverine HCl
CAS:<p>Diproteverine HCl is a novel calcium antagonist with antianginal properties, antispasmodic and vasoactive.</p>Fórmula:C26H36ClNO4Pureza:98.55% - 99.84%Forma y color:SolidPeso molecular:462.02sEH inhibitor-7
CAS:<p>sEH inhibitor-7 is a soluble epoxide hydrolase (sEH) inhibitor that inhibits sEH in human and mouse with IC 50 s of 6.2 μM and 0.15 μM, respectively.</p>Fórmula:C15H21NO2Pureza:99.56%Forma y color:SolidPeso molecular:247.33JNJ-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>Fórmula:C26H24FN5O2SPureza:99.62%Forma y color:SolidPeso molecular:489.56Xanthine oxidoreductase-IN-3
CAS:<p>Xanthine oxidoreductase-IN-3, an oral XOR inhibitor with IC50 of 26.3 nM, is useful for acute hyperuricemia research.</p>Fórmula:C14H10ClN5OPureza:98.1%Forma y color:SolidPeso molecular:299.72C75
CAS:<p>C75 is an inhibitor synthetic fatty-acid synthase (FASN) and inhibits prostate cancer cells PC3 (IC50: 35 μM).</p>Fórmula:C14H22O4Pureza:98.84% - >99.99%Forma y color:SolidPeso molecular:254.32Autotaxin-IN-3
CAS:<p>Autotaxin-IN-3 is an inhibitor of Autotaxin (IC50 = 2.4 nM) which is responsible for the increase in lysophosphatidic acid in ascites and plasma.</p>Fórmula:C22H21N9O2Pureza:99.54% - 99.79%Forma y color:SolidPeso molecular:443.46Qc1
CAS:<p>Qc1 is an inhibitor of threonine dehydrogenase (TDH) inhibitor and can be used in studies about metabolic diseases.</p>Fórmula:C23H16F3N3O2SPureza:99.75%Forma y color:SolidPeso molecular:455.45Farglitazar
CAS:<p>Farglitazar (GI-262570) is a PPAR-γ agonist and insulin sensitizer used in the study of diabetes.</p>Fórmula:C34H30N2O5Pureza:99.4% - 99.52%Forma y color:SolidPeso molecular:546.61Dalvastatin
CAS:<p>Dalvastatin (RG-12561) is an orally available inhibitor of HMG-CoA reductase and cholesterol-lowering synthesis.Dalvastatin competitively inhibits rat hepatic</p>Fórmula:C24H31FO3Pureza:98.80%Forma y color:SolidPeso molecular:386.5G6PD activator AG1
CAS:<p>G6PD activator AG1 is a G6PD agonist that promotes G6PD oligomerization to a catalytically competent form.</p>Fórmula:C24H30N4S2Pureza:98.38% - 99.51%Forma y color:SolidPeso molecular:438.65Cronidipine
CAS:<p>Cronidipine (LF 20254), a calcium channel antagonist, is used potentially for the treatment of hypertension and myocardia ischemia.</p>Fórmula:C30H32ClN3O8Pureza:99.47%Forma y color:SolidPeso molecular:598.04AM 374
CAS:<p>AM 374 (HDSF), a fatty acid amide hydrolase (FAAH) inhibitor, demonstrates the capacity to inhibit amidase activity, boasting an IC50 value of 13 nM.</p>Fórmula:C16H33FO2SPureza:98.39%Forma y color:SolidPeso molecular:308.5Fluorobexarotene
CAS:<p>Fluorobexarotene, a potent RXR agonist, has 75% higher affinity than Bexarotene with Ki of 12 nM and EC50 of 43 nM for RXRα.</p>Fórmula:C24H27FO2Pureza:99.08%Forma y color:SolidPeso molecular:366.47Mopidamol
CAS:<p>Mopidamol (RA 233) is a phosphodiesterase inhibitor, a dipyridamole derivative, with anticancer activity that prevents retinal vascular defects in experimental</p>Fórmula:C19H31N7O4Pureza:99.05% - 99.78%Forma y color:SolidPeso molecular:421.49Fidexaban
CAS:<p>Fidexaban (CI1031) is a novel, potent, selective and orally active factor Xa inhibitor that has demonstrated antithrombotic activity in a variety of assays</p>Fórmula:C25H24F2N6O5Pureza:98.64% - 99.43%Forma y color:SolidPeso molecular:526.49hCAI/II-IN-6
CAS:<p>hCAI/II-IN-6 is a selective and orally active inhibitor of human carbonic anhydrase (CA).</p>Fórmula:C19H24N4O3SPureza:97.07%Forma y color:SolidPeso molecular:388.48hCAII-IN-9
CAS:<p>hCAII-IN-9 inhibits hCA II/IX/XII with IC50s of 1.18, 0.17, 2.99 μM; not BBB permeable.</p>Fórmula:C15H16ClN3O5S2Pureza:98.63%Forma y color:SolidPeso molecular:417.89Dasantafil
CAS:Dasantafil (SCH446132) is a small molecule phosphodiesterase-5A (PDE5A) inhibitor used to treat genitourinary disorders and study erectile dysfunction.Fórmula:C22H28BrN5O5Pureza:99.4% - 99.50%Forma y color:SolidPeso molecular:522.39Acetyl-L-carnitine
CAS:<p>Acetyl-L-carnitine, an amino-acid supplement, crosses the blood-brain barrier to aid in neuroinflammation and Alzheimer's.</p>Fórmula:C9H17NO4Pureza:>99.99%Forma y color:SolidPeso molecular:203.24CERM-11956
CAS:<p>Pelretin (BASF 43915) is a potential protein inhibitor for the study of dermatologic diseases.</p>Fórmula:C29H38N2O7Pureza:99.38%Forma y color:SolidPeso molecular:526.62Indeglitazar
CAS:<p>Indeglitazar (PPM 204) is orally available pan-agonist of PPAR (PPAR subtypes alpha (α), delta (δ), and gamma (γ)).</p>Fórmula:C19H19NO6SPureza:99.45%Forma y color:SolidPeso molecular:389.42Libenzapril
CAS:<p>Libenzapril (CGS 16617) is a potent angiotensin-converting enzyme inhibitor used to study myocardial injury.</p>Fórmula:C18H25N3O5Pureza:99.78%Forma y color:SolidPeso molecular:363.41NG-497
CAS:<p>NG-497, a selective inhibitor of human ATGL, blocks lipolysis in adipocytes and aids cancer research.</p>Fórmula:C18H21NO4Pureza:99.56%Forma y color:SolidPeso molecular:315.36PC945
CAS:<p>PC945 (Opelconazole) is an antifungal compound that inhibits CYP51A/CYP51B and can be used to study fungal infections of the lungs.</p>Fórmula:C38H37F3N6O3Pureza:98.89% - 99.37%Forma y color:SolidPeso molecular:682.73PDE5-IN-2
CAS:<p>PDE5-IN-2 is a potent, highly selective, and orally active inhibitor of PDE5(IC50 of 0.31 nM)</p>Fórmula:C25H21N3O6SPureza:98%Forma y color:SolidPeso molecular:491.52LMPTP INHIBITOR 1 hydrochloride
CAS:<p>LMPTP INHIBITOR 1 hydrochloride is a selective inhibitor of low molecular weight protein tyrosine phosphatase ( LMPTP ), with an IC 50 of 0.8 μM for LMPTP-A.</p>Fórmula:C28H37ClN4OPureza:99.89%Forma y color:SolidPeso molecular:481.07S-2E
CAS:<p>S-2E, an oral inhibitor of HMG-CoA reductase/acetyl-CoA carboxylase, treats hyperlipidemia.</p>Fórmula:C22H25NO4Forma y color:SolidPeso molecular:367.44HIF-2α-IN-6
CAS:<p>HIF-2α-IN-6 (117) is a HIF-2α inhibitor [1].</p>Fórmula:C15H13F4NO3SForma y color:SolidPeso molecular:363.33Monoacylglycerol lipase inhibitor 1
CAS:<p>Monoacylglycerol lipase inhibitor 1, also known as compound 13 [1], is a potent inhibitor of monoacylglycerol lipase.</p>Fórmula:C21H28N2O3Forma y color:SolidPeso molecular:356.46Lp-PLA2-IN-14
CAS:<p>Lp-PLA2-IN-14 (Compound 19), an inhibitor of rhLp-PLA2, exhibits a potent inhibitory effect with a pIC50 value of 8.4.</p>Fórmula:C16H14F3N3O3Pureza:98%Forma y color:SolidPeso molecular:353.3NUCC-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:426.91RORγt inverse agonist 14
CAS:<p>RORγt inverse agonist 14 (8e) is a potent, selective, and orally active compound with an EC50 of 2.5 nM, exhibiting anti-inflammatory activity.</p>Fórmula:C26H26F8N2O6S2Pureza:98%Forma y color:SolidPeso molecular:678.61AR453588
CAS:<p>AR453588 is an orally bioavailable anti-diabetic glucokinase activator (EC50: 42 nM) with anti-hyperglycemic activity.</p>Fórmula:C25H25N7O2S2Forma y color:SolidPeso molecular:519.649(Z),11(Z)-Octadecadienoic acid
CAS:<p>9(Z),11(Z)-Octadecadienoic acid, an isomer of linoleic acid, demonstrates antitumor activity with an EC50 value of 446.1 µM [1].</p>Fórmula:C18H32O2Forma y color:SolidPeso molecular:280.45IDH1 Inhibitor 5
CAS:<p>IDH1 Inhibitor 5 targets MOG cells (IC50: 64.4 nM) and R132H mutant IDH1 gliomas (IC50: 34.9 nM).</p>Fórmula:C26H34N4O3Forma y color:SolidPeso molecular:450.57JP104
CAS:<p>JP104 is an aryl carbamate that irreversibly inhibits fatty acid amide hydrolase (FAAH) with a pIC50 value of approximately 8 [1].</p>Fórmula:C25H30N2O3Pureza:98%Forma y color:SolidPeso molecular:406.52Benzoic acid lithium
CAS:<p>Lithium benzoate, an aromatic alcohol present in numerous plants, commonly serves as an additive in food, beverages, cosmetics, and various other products. This compound exhibits antibacterial and antifungal properties, functioning effectively as a preservative [1].</p>Fórmula:C7H5LiO2Forma y color:SolidPeso molecular:128.06XL041
CAS:<p>XL041 (BMS-852927) is an agonist of LXRβ-selective.</p>Fórmula:C29H28Cl2F2N2O4SPureza:98%Forma y color:SolidPeso molecular:609.51h-NTPDase-IN-5
CAS:<p>h-NTPDase-IN-5 (compound 3b) serves as a pan-inhibitor of NTPDase, exhibiting inhibitory concentration 50 (IC50) values of 1.10 μM (h-NTPDase1), 44.73 μM (h-</p>Fórmula:C23H21N3O2SPureza:98%Forma y color:SolidPeso molecular:403.5GSK2647544
CAS:<p>GSK2647544 inhibits Lp-PLA2, a pro-inflammatory enzyme from macrophages, orally active, calcium-independent.</p>Fórmula:C24H18ClF3N4O3Forma y color:SolidPeso molecular:502.87PHD2-IN-1
CAS:<p>PHD2-IN-1, a potent and orally active HIF prolyl hydroxylase 2 (PHD2) inhibitor, exhibits an IC50 of 22.53 nM and is applicable in anemia research [1].</p>Fórmula:C21H23ClN4O5Pureza:98%Forma y color:SolidPeso molecular:446.88H2-003
CAS:<p>H2-003 is a selective inhibitor of diacylglycerol acyltransferase 2 (DGAT2).</p>Fórmula:C25H26N4O4Forma y color:SolidPeso molecular:446.5R1498
CAS:<p>R1498 inhibits CDK2, targets angiogenesis and mitosis, and is an oral treatment for liver and stomach cancer.</p>Fórmula:C18H15ClN4OPureza:98%Forma y color:SolidPeso molecular:338.79A 78773
CAS:<p>A 78773: potent reversible 5-lipoxygenase inhibitor; active in cells/tissues; targets inflammation, asthma, IBD.</p>Fórmula:C15H13FN2O4Forma y color:SolidPeso molecular:304.27Mutant IDH1-IN-4
CAS:<p>Mutant IDH1-IN-4 is an mutant Isocitrate dehydrogenase 1 (IDH 1) inhibitor.</p>Fórmula:C25H34N4O3Pureza:98%Forma y color:SolidPeso molecular:438.563,5-Dinitrocatechol
CAS:<p>OR-486 is an inhibitor of catechol-O-methyl-transferase(COMT) and can be used to prepare the molybdenum (VI)- 3,5-Dinitrocatechol complex.</p>Fórmula:C6H4N2O6Pureza:99.8%Forma y color:SolidPeso molecular:200.11ICMT-IN-36
CAS:<p>ICMT-IN-36 (compound 40) serves as an ICMT inhibitor, with an IC50 value of 0.181 μM [1].</p>Fórmula:C21H25Cl2NOForma y color:SolidPeso molecular:378.34Pactimibe sulfate
CAS:<p>Pactimibe sulfate is a dual ACAT1/2 inhibitor with anti-atherogenic potential, reducing plasma cholesterol.</p>Fórmula:C50H82N4O10SForma y color:SolidPeso molecular:931.28Quetiapine sulfoxide dihydrochloride
CAS:<p>Quetiapine sulfoxide dihydrochloride, a major metabolite of second-gen antipsychotic Quetiapine, modulates 5-HT and dopamine receptors.</p>Fórmula:C21H27Cl2N3O3SPureza:98%Forma y color:SolidPeso molecular:472.43MK-8189
CAS:<p>MK-8189 is a potent and selective pyrimidine PDE10A inhibitor, with excellent PDE (phosphodiesterase) selectivity for the treatment of schizophrenia.</p>Fórmula:C19H22N6OSPureza:99.38% - 99.67%Forma y color:SolidPeso molecular:382.48
