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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ALDH1A3-IN-2
CAS:<p>ALDH1A3-IN-2 is a potent ALDH1A3 inhibitor with an IC50 of 0.30 μM.ALDH1A3-IN-2 has potential for cancer disease research.</p>Fórmula:C13H17NOPureza:99.84%Forma y color:SolidPeso molecular:203.2811-cis-Vaccenyl acetate
CAS:<p>11-cis-Vaccenyl acetate ((Z)-Octadec-11-enyl acetate) activates olfactory neurons located in the T1 sensilla on the antenna and mediates aggregation behavior in</p>Fórmula:C20H38O2Pureza:96.53% - 99.95%Forma y color:LiquidPeso molecular:310.51JNJ-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:489.56Lifarizine
CAS:<p>Lifarizine (RS-87476), a calcium-sodium channel antagonist, shows neuroprotective activity in a simplified rat survival model of double vessel occlusion.</p>Fórmula:C29H32N4Pureza:99.88%Forma y color:SolidPeso molecular:436.59Edoxaban
CAS:<p>Edoxaban: potent, selective FXa inhibitor; Ki 0.561 nM. Used as an oral anticoagulant for stroke prevention, also inhibits thrombin and FIXa.</p>Fórmula:C24H30ClN7O4SPureza:97.67% - 99.71%Forma y color:SolidPeso molecular:548.06PDE4B-IN-2
CAS:<p>PDE4B-IN-2 (A 33), an oral PDE4B inhibitor, IC50: 15 nM; less potent on PDE4D (IC50: 1.7 µM), has anti-inflammatory properties.</p>Fórmula:C19H18ClN3O2SPureza:99.32%Forma y color:SolidPeso molecular:387.88IMPDH2-IN-2
CAS:<p>IMPDH2-IN-2 is an IMPDH inhibitor with antimicrobial activity and potential anti-tuberculosis activity for the study of inflammation and immune dysfunction.</p>Fórmula:C21H15Cl2N3O3Pureza:99.02%Forma y color:SolidPeso molecular:428.27ARRY-403
CAS:<p>ARRY-403 is a novel glucokinase activator that reduces fasting and postprandial blood glucose in patients with type 2 diabetes.</p>Fórmula:C20H18N6O3S2Pureza:98.80%Forma y color:SolidPeso molecular:454.52Giripladib
CAS:<p>Giripladib (PLA695/PLX-695) blocks radiation-boosted phosphorylation of ERK and Akt in endothelial cells.</p>Fórmula:C41H36ClF3N2O4SPureza:99.64%Forma y color:SolidPeso molecular:745.25Tofimilast
CAS:<p>Tofimilast (CP-325366), a PDE4 inhibitor, is used potentially for the treatment of asthma and chronic obstructive pulmonary disease.</p>Fórmula:C18H21N5SPureza:99.55%Forma y color:SolidPeso molecular:339.46Olorofim
CAS:<p>Olorofim（F-901318）is a new selective antifungal compound that inhibits Aspergillus fumigatus DHODH (IC50: 44 nM). Cost-effective and quality-assured.</p>Fórmula:C28H27FN6O2Pureza:99.28%Forma y color:SolidPeso molecular:498.55AMG-1694
CAS:<p>AMG-1694 disrupts GK-GKRP complex, enhancing GK activity with 7 nM IC50; normalizes glucose in diabetic rodents without affecting normoglycemic animals.</p>Fórmula:C23H30F3N3O4S2Pureza:98.37%Forma y color:SolidPeso molecular:533.63Chloramphenicol succinate
CAS:<p>Chloramphenicol succinate is a bacteriostatic antibiotic. CPSA is a competitive substrate and inhibitor of succinate dehydrogenase (SDH),can be oxidized by.</p>Fórmula:C15H16Cl2N2O8Pureza:95.32%Forma y color:Physical Description White Powder (Ntp 1992)Peso molecular:423.2IQB-782
CAS:<p>IQB-782 is a mucolytic agent with mucolytic expectorant activity for the study of obstructive lung disease.</p>Fórmula:C4H9N3O2SPureza:>99.99%Forma y color:SolidPeso molecular:163.2Pradefovir
CAS:<p>Pradefovir (Remofovir) is a prodrug for chronic HBV, converting to PMEA in the liver with a Km of 60 μM and clearance of 359 ml/min.</p>Fórmula:C17H19ClN5O4PPureza:97.50%Forma y color:SolidPeso molecular:423.79S-2474
CAS:<p>S-2474, an inhibitor of COX-2 and 5-lipoxygenase, has anti-inflammatory and neuroprotective activities, and inhibits cell death.</p>Fórmula:C20H31NO3SPureza:99.03%Forma y color:SolidPeso molecular:365.53Fumarate hydratase-IN-1
CAS:Fumarate hydratase-IN-1 is a cell-permeable fumarate hydratase inhibitor with antiproliferative activity and can be used to study cellular activity.Fórmula:C27H30N2O4Pureza:98.96% - 99.49%Forma y color:SolidPeso molecular:446.54Bupicomide
CAS:<p>Bupicomide is a dopamine β-hydroxylase inhibitor with antihypertensive and vasodilatory activity and may be used in the study of hypertension.</p>Fórmula:C10H14N2OPureza:99.84% - >99.99%Forma y color:SolidPeso molecular:178.23Tigulixostat
CAS:<p>Tigulixostat (LC350189) is a novel xanthine oxidase inhibitor (XOI) that reduces uric acid production and may be used to study gout-related diseases.</p>Fórmula:C16H14N4O2Pureza:98.22% - 99.71%Forma y color:SolidPeso molecular:294.31MM 11253
CAS:<p>MM 11253 is a RARγ antagonist with IC50 of 44nM.</p>Fórmula:C28H30O2S2Pureza:99.41%Forma y color:SolidPeso molecular:462.67Sultiame
CAS:<p>Sultiame is an inhibitor of carbonic anhydrase. Sultiame can be used in antiepileptic research.</p>Fórmula:C10H14N2O4S2Pureza:99.91%Forma y color:SolidPeso molecular:290.36AWD 12-281
CAS:<p>AWD 12-281 is a PDE4 inhibitor with anti-inflammatory activity and bronchodilator activity for the study of chronic obstructive pulmonary disease (COPD).</p>Fórmula:C22H14Cl2FN3O3Pureza:99.25% - 99.85%Forma y color:SolidPeso molecular:458.27SR2211
CAS:<p>SR2211 is a specific modulator and an inverse agonist of RORγ(IC50 = 320 nM, Ki = 105 nM).</p>Fórmula:C26H24F7N3OPureza:98.75%Forma y color:SolidPeso molecular:527.48hCAI/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:388.48Nampt activator-2
CAS:<p>Nampt activator-2: Potent NAMPT activator (EC50: 0.023 μM), binds CYP2C9 (0.060 μM), 2D6 (0.41 μM), 2C19 (0.59 μM); useful in metabolic disease research.</p>Fórmula:C17H15ClN4O3SPureza:98.30% - 98.33%Forma y color:SolidPeso molecular:390.84PD173212
CAS:<p>PD 173212 is a blocker that blocks N-type voltage sensitive calcium channel (Cav2.2).</p>Fórmula:C38H53N3O3Pureza:99.84%Forma y color:SolidPeso molecular:599.85Ladostigil
CAS:<p>Ladostigil is an oral cholinesterase & MAO-B inhibitor used for depression and Alzheimer's studies.</p>Fórmula:C16H20N2O2Pureza:97.48%Forma y color:SolidPeso molecular:272.34PC945
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:682.73K-111
CAS:<p>K-111 is a PPAR alpha agonist. K-111 improves insulin resistance, reducing bodyweight, and ameliorating atherogenic dyslipidemia.</p>Fórmula:C18H25Cl3O2Pureza:99.64% - 99.88%Forma y color:SolidPeso molecular:379.75Isomazole
CAS:<p>Isomazole is a novel orally available phosphodiesterase (PDE) inhibitor with calcium-sensitizing properties that inhibits PDE3 and PDE4.</p>Fórmula:C14H13N3O2SPureza:98.66%Forma y color:SolidPeso molecular:287.34MAO-B-IN-8
CAS:<p>MAO-B-IN-8 is a highly potent and reversible inhibitor of monoamine oxidase-B (MAO-B), which also exhibits inhibitory effects on the microglial production of</p>Fórmula:C18H16O6Pureza:99.62%Forma y color:SolidPeso molecular:328.32Opc 8490
CAS:<p>Opc 8490 is a cardiotonic agent and a positive inotropic vasodilator, which prolongs the atrial action potential in a concentration-dependent manner.</p>Fórmula:C30H35N3O10Pureza:98.88%Forma y color:SolidPeso molecular:597.61DS16570511
CAS:<p>DS16570511 is a novel, cell-permeable inhibitor targeting the mitochondrial calcium uniporter.</p>Fórmula:C30H25Cl2N3O4Pureza:98.34% - 98.45%Forma y color:SolidPeso molecular:562.44Carbazeran
CAS:<p>Carbazeran (UK-31,557) is an inhibitor of PDE2 and PDE3 and can be used for studies about metabolic diseases.</p>Fórmula:C18H24N4O4Pureza:99.3%Forma y color:SolidPeso molecular:360.41BRD7389
CAS:<p>BRD7389 is an inhibitor of RSK family kinase with IC50s of 1.5 μM, 2.4 μM, and 1.2 μM for RSK1, RSK2, and RSK3, respectively.</p>Fórmula:C24H18N2O2Pureza:99.51%Forma y color:SolidPeso molecular:366.41G6PD 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:438.65AGN 196996
CAS:<p>AGN 196996: strong RARα inhibitor (Ki: 2 nM), weak for RARβ/γ (Ki: 1087/8523 nM).</p>Fórmula:C24H20BrNO5Pureza:98.74%Forma y color:SolidPeso molecular:482.32PF-04447943
CAS:<p>PF-04447943, a selective PDE9A inhibitor (IC50=12nM), may aid sickle cell anemia research with its anti-inflammatory properties.</p>Fórmula:C20H25N7O2Pureza:99.36% - 99.59%Forma y color:SolidPeso molecular:395.46alphaSYN-IN-NAB2
CAS:<p>alphaSYN-IN-NAB2: a NAB2 gene protein guarding neurons against alpha-SYN harm; aids endosomal transport, cell processes, and can study various diseases.</p>Fórmula:C23H20ClN3OPureza:98.49%Forma y color:SolidPeso molecular:389.88MLS000544460
CAS:<p>MLS000544460 is a highly selective and reversible Eya2 phosphatase inhibitor (Kd: 2.0 μM, IC50: 4 μM).MLS000544460 exhibits inhibitory effects on Eya2</p>Fórmula:C17H12FN3O2SPureza:99.72%Forma y color:SolidPeso molecular:341.36Salnacedin
CAS:<p>Salnacedin (G-201) treats immune, skin, and musculoskeletal issues, suitable for acne, dermatitis, and psoriasis research.</p>Fórmula:C12H13NO5SPureza:99.13%Forma y color:SolidPeso molecular:283.3L-Threonine derivative-1
CAS:L-Threonine derivative-1 is acetylsalicylic acid-L-threonine ester with potential analgesic activity.Fórmula:C13H15NO6Pureza:97.03% - 98.91%Forma y color:SolidPeso molecular:281.26KRH102140
CAS:<p>KRH102140 is a PHD2 activator that reduces angiogenesis by inhibiting HIF-1alpha, used in cardiovascular disease research.</p>Fórmula:C25H24FNOPureza:98.31% - 99.61%Forma y color:SolidPeso molecular:373.46KT182
CAS:<p>KT182 is a selective and potent inhibitor of α/β-hydrolase domain containing 6 (ABHD6), with an IC50 of 0.24 nM in Neuro2A cells.</p>Fórmula:C27H26N4O2Pureza:99.66%Forma y color:SolidPeso molecular:438.52BAY-0069
CAS:<p>BAY-0069 is a potent and selective PPARγ transactivator that inhibits human PPARγ and murine PPARγ with IC50s of 6.3 nM and 24 nM, respectively.BAY-0069 can be</p>Fórmula:C22H16BrN3O4Pureza:99.41%Forma y color:SoildPeso molecular:466.28KT203
CAS:<p>KT203 is an α/β hydrolase structural domain 6 (ABHD6) inhibitor with potential antiviral and anti-inflammatory activity for the study of pneumonia.</p>Fórmula:C28H26N4O3Pureza:98.51%Forma y color:SolidPeso molecular:466.53Qc1
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:455.45Imanixil
CAS:<p>Imanixil boosts LDLR, cuts cholesterol and VLDL production, reducing atherosclerosis.</p>Fórmula:C17H17F3N6O2Pureza:>99.99% - >99.99%Forma y color:SolidPeso molecular:394.35NNC 05-2090 hydrochloride
CAS:<p>NNC 05-2090 HCl: BGT-1 inhibitor, IC50 = 10.6 μM, potential for epilepsy, neurological research.</p>Fórmula:C27H31ClN2O2Pureza:99.05%Forma y color:SolidPeso molecular:451BAY-4931
CAS:<p>BAY-4931 is a powerful, covalent, and selective inverse-agonist of PPARγ, exhibiting an IC50 value of 0.17 nM.</p>Fórmula:C22H16ClN3O4Pureza:99.47%Forma y color:SoildPeso molecular:421.83
