
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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UCPH-102
CAS:<p>UCPH-102: Selective EAAT1 inhibitor, IC50 0.43 μM, treats Alzheimer's, ALS, chronic pain, OCD; crosses blood-brain barrier, targets T-ALL cells.</p>Fórmula:C21H18N2O2Forma y color:SolidPeso molecular:330.38Phenylpyropene C
CAS:<p>Phenylpyropene C inhibits JAK/STAT and IFN-γ expression (IC50: 5.4-10.8 μM), also blocks acyl CoA (IC50: 16.0 μM).</p>Fórmula:C28H34O5Forma y color:SolidPeso molecular:450.57ICMT-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:378.34CM-10-18
CAS:<p>CM-10-18: potent ER α-glucosidase inhibitor, strong antiviral against hemorrhagic fever viruses, protects mice from dengue fatality.</p>Fórmula:C17H35NO5Forma y color:SolidPeso molecular:333.46FM26
CAS:FM26, an isoxazole-based RORγt inverse agonist, cuts EL4 IL-17a mRNA; potent with 264 nM IC50.Fórmula:C22H15ClF3N3O3Pureza:98%Forma y color:SolidPeso molecular:461.826β-hydroxy Testosterone
CAS:<p>6β-hydroxy Testosterone (4-Androsten-6β,17β-diol-3-one) is a 17β-hydroxy steroid, an androgen and endogenous metabolite.</p>Fórmula:C19H28O3Forma y color:SoildPeso molecular:304.42Dioleyldimethylammonium chloride
CAS:<p>Dioleyldimethylammonium chloride (DODAC) is a cationic lipid utilized as a transfection reagent [1].</p>Fórmula:C38H76ClNForma y color:SolidPeso molecular:582.47ICMT-IN-19
CAS:<p>ICMT-IN-19 (compound 53) serves as a potent inhibitor of ICMT, demonstrating an IC50 value of 0.026 μM [1].</p>Fórmula:C21H26N2O3Forma y color:SolidPeso molecular:354.44AKB-6899
CAS:<p>AKB-6899 is an inhibitor of prolyl hydroxylase domain 3 (PHD3) and increases the soluble form of the VEGF receptor (sVEGFR-1) production from GM-CSF-treated</p>Fórmula:C14H11FN2O4Pureza:97.87%Forma y color:SolidPeso molecular:290.25AMC Arachidonoyl Amide
CAS:<p>Arachidonoyl amide (AMC-AA) is a fatty acid amide among several that serve to quantify fatty acid amide hydrolase (FAAH) activity. FAAH, with its relative lack of selectivity, processes various amide head groups beyond ethanolamine, the head group of its primary endogenous substrate, anandamide (AEA). The interaction of AMC-AA with FAAH leads to the liberation of fluorescent aminomethyl coumarin, which has an absorption peak at 360 nm and emission at 465 nm. This fluorescence release facilitates the rapid and efficient assessment of FAAH activity through the utilization of either a standard cuvette or a microplate fluorometer.</p>Fórmula:C30H39NO3Forma y color:SolidPeso molecular:461.6LY-338979
CAS:<p>LY-338979 is an impurity of pemetrexedone.</p>Fórmula:C20H21N5O7Pureza:98%Forma y color:SolidPeso molecular:443.41PPAR agonist 1
CAS:<p>PPAR agonist 1 is an agonist of PPAR α/γ, used for reducing blood glucose, lipid levels, reducing body weight, and lowering cholesterol.</p>Fórmula:C20H25NO6SPureza:98%Forma y color:SolidPeso molecular:407.48PDE5-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:491.52Mal-Pc
CAS:<p>Mal-Pc, a maleimide phthalocyanine, depletes GSH to reduce aggregation and boost ROS, improving PDT against cancer.</p>Fórmula:C46H28N10O8SiPureza:98%Forma y color:SolidPeso molecular:876.86Lp-PLA2-IN-13
CAS:<p>Lp-PLA2-IN-13 (compound 15), a potent Lp-PLA2 inhibitor, holds potential for research in neurodegenerative-related diseases [1].</p>Fórmula:C22H17F5N4O4Pureza:98%Forma y color:SolidPeso molecular:496.39L-690488
CAS:<p>L-690488 has more effective cell penetration than L-690330. L-690488 is a prodrug of L-690330 and is a selective inositol monophosphatase (IMPase) inhibitor.</p>Fórmula:C32H52O16P2Pureza:98%Forma y color:SolidPeso molecular:754.69GLUT4 activator 1
CAS:<p>GLUT4 activator 1 is a potent glucose transporter type 4 (GLUT4) translocation activator (EC50: 0.14 μM).</p>Fórmula:C23H21FN4O3SPureza:98%Forma y color:SolidPeso molecular:452.5RORγt Inverse agonist 6
CAS:<p>RORγt Inverse agonist 6 is an agonist of RORγt inverse. RORγt Inverse agonist 6 can be used in research on Th17-driven autoimmune diseases.</p>Fórmula:C28H29ClN6O5Pureza:99.52%Forma y color:SolidPeso molecular:565.02S-Benzylglutathione
CAS:<p>S-Benzylglutathione acts as a competitive inhibitor of glutathionase and undergoes conversion by rat kidney microsomes into its cysteine derivatives.</p>Fórmula:C17H23N3O6SForma y color:SolidPeso molecular:397.45Prostaglandin F2α-1-glyceryl ester
CAS:<p>Prostaglandin F2α-1-glyceryl ester undergoes oxidation via 15-hydroxyprostaglandin dehydrogenase (15-HPGDH) [1].</p>Fórmula:C23H40O7Forma y color:SolidPeso molecular:428.566Quizalofop-P
CAS:<p>Quizalofop-P, a selective herbicide, is absorbed by weed stems and leaves before translocating both upward and downward within the plant, concentrating in</p>Fórmula:C17H13ClN2O4Pureza:98%Forma y color:SolidPeso molecular:344.75Benzyl-α-GalNAc
CAS:<p>Benzyl-α-GalNAc (O-glycosylation-IN-1) is a potent inhibitor of O-glycosylation and is used to reduce mucin on cell surfaces.</p>Fórmula:C15H21NO6Pureza:99.84%Forma y color:SolidPeso molecular:311.33DORI
CAS:<p>DORI, a cationic lipid, efficiently delivers plasmid DNA in vitro, exhibiting lower cytotoxicity and high transfection efficiency [1].</p>Fórmula:C43H82BrNO5Forma y color:SolidPeso molecular:773.021,2-Dilauroyl-sn-glycero-3-phospho-(2R)-glycerol sodium
CAS:<p>1,2-Dilauroyl-sn-glycero-3-phospho-(2R)-glycerol is a type of phosphoglycerol characterized by the presence of lauric acid at the sn-1 and sn-2 positions. [Matreya, LLC. Catalog No. 1443]</p>Fórmula:C30H58O10PNaForma y color:SolidPeso molecular:632.74Safinamide Acid
CAS:<p>Safinamide acid, a potential impurity in commercial safinamide preparations and a degradation product of safinamide under thermal and oxidative stress, is encountered in the pharmaceutical formulation process.</p>Fórmula:C17H18FNO3Forma y color:SolidPeso molecular:303.33DNCA
CAS:<p>DNCA, a neutral lipid, facilitates the creation of lipid nanoparticles (LNPs) and is instrumental in [nucleic acid delivery](1).</p>Fórmula:C45H82N4O4Forma y color:SolidPeso molecular:743.163-Hydroxycarbofuran
CAS:<p>3-Hydroxycarbofuran, a principal metabolite of Carbofuran, acts as a reversible inhibitor of acetylcholinesterase (AChE) [1].</p>Fórmula:C12H15NO4Pureza:98%Forma y color:SolidPeso molecular:237.25ICMT-IN-20
CAS:<p>ICMT-IN-20 (compound 54) serves as an ICMT inhibitor with an IC50 value of 0.682 μM [1].</p>Fórmula:C21H26N2O3Forma y color:SolidPeso molecular:354.44Frunexian
CAS:<p>Frunexian (EP-7041) is a selective and potent inhibitor of coagulation factor XI/activated factor XI, specifically targeting XIa.</p>Fórmula:C19H26N4O4Pureza:98%Forma y color:SolidPeso molecular:374.43h15-LOX-2 inhibitor 1
CAS:<p>Compound 105 (h15-LOX-2 inhibitor 1) is a potent inhibitor of human epithelial 15-lipoxygenase-2 (h15-LOX-2), exhibiting an IC50 of 0.34 μM [1].</p>Fórmula:C17H13F3N2SPureza:98%Forma y color:SolidPeso molecular:334.36UK 357903
CAS:<p>UK 357903, a phosphodiesterase 5A (PDE5A) inhibitor, is used potentially for the treatment of erectile dysfunction.</p>Fórmula:C27H34N8O5SForma y color:SolidPeso molecular:582.67RXPA 380
CAS:<p>RXPA 380: C-terminal ACE inhibitor, Ki=3nM; IC50=2.5nM for C-domain ACE mutants.</p>Fórmula:C33H36N3O7PForma y color:SolidPeso molecular:617.631,2,3-Tritricosanoyl Glycerol
CAS:<p>1,2,3-Tritricosanoyl glycerol, a triacylglycerol containing tricosanoic acid at the sn-1, sn-2, and sn-3 positions, serves as an internal standard for the quantification of fatty acids within the triglyceride component of human aortic endothelial cells (HAECs) cultured in media supplemented with stearic and/or oleic acid.</p>Fórmula:C72H140O6Forma y color:SolidPeso molecular:1101.88A 79175
CAS:<p>A 79175 is a 5-lipoxygenase inhibitor that increases bone formation.</p>Fórmula:C15H13FN2O4Pureza:98%Forma y color:SolidPeso molecular:304.27Efipladib
CAS:<p>Efipladib is a phospholipase inhibitor. Efipladib decreases nociceptive responses without affecting PGE2 levels in the cerebral spinal fluid.</p>Fórmula:C40H35Cl3N2O4SForma y color:SolidPeso molecular:746.14SCD1/5-IN-1
CAS:<p>SCD1/5-IN-1 (Compound 10), a selective SCD1/5 inhibitor, is utilized in the research of neurological diseases [1].</p>Fórmula:C12H10N4O3Forma y color:SolidPeso molecular:258.237GCase modulator-1
CAS:<p>GCase Modulator-1 (Compound 9g), a quinazoline derivative, functions as a glucosidase modulator with an AC50 value of 2.23 µM [1].</p>Fórmula:C22H18N4Pureza:98%Forma y color:SolidPeso molecular:338.41ICMT-IN-27
CAS:<p>ICMT-IN-27, also known as compound 64, is an inhibitor of the enzyme ICMT, demonstrating potent activity with an IC50 value of 0.1 µM [1].</p>Fórmula:C22H28FNO2Forma y color:SolidPeso molecular:357.46FAAH/cPLA2α-IN-1
CAS:<p>FAAH/cPLA2α-IN-1 is a compound that simultaneously inhibits both FAAH and cPLA2α, demonstrating potent activity with half-maximal inhibitory concentrations (</p>Fórmula:C19H26N4O5Pureza:98%Forma y color:SolidPeso molecular:390.43AS1468240
CAS:<p>AS1468240 is a factor Xa inhibitor. It has significant oral anticoagulant activity.</p>Fórmula:C25H25Cl2N5O3Forma y color:SolidPeso molecular:514.4CETP-IN-3
CAS:<p>CETP-IN-3 is an inhibitor of the plasma glycoprotein cholesterol ester transfer protein (CETP), elevating HDL-C through inhibition of CETP.</p>Fórmula:C30H24F12N2O4Pureza:98%Forma y color:SolidPeso molecular:704.5JNJ-42259152
CAS:<p>JNJ-42259152 is a phosphodiesterase 10A PET tracer.</p>Fórmula:C24H23FN4OForma y color:SolidPeso molecular:402.46NC1
CAS:<p>NC1 is a potent allosteric inhibitor of lymphoid-specific PTPN22, a protein tyrosine phosphatase.</p>Fórmula:C29H26N2O7SForma y color:SolidPeso molecular:546.59GLX481304
CAS:<p>GLX481304 is a selective Nox-2 and Nox-4 inhibitor, exhibiting IC50 values of 1.25 μM.</p>Fórmula:C23H29N7OForma y color:SolidPeso molecular:419.52Inz-1
CAS:Inz-1 is an effective and fungal-selective inhibitor of mitochondrial cytochrome bc1 with IC50s of 8.092 and 45.320 μM for yeast and human.Fórmula:C16H14N2O2Pureza:99.55% - 99.88%Forma y color:SolidPeso molecular:266.29PD 109488
CAS:<p>PD 109488 is a metabolite of quinapril and is a derivative of Quinapril that acts as an ACE inhibitor.</p>Fórmula:C25H28N2O4Pureza:98%Forma y color:SolidPeso molecular:420.5G1-OC2-K3-E10
CAS:<p>G1-OC2-K3-E10, an ionizable lipid, facilitates mRNA delivery through lipid nanoparticles (LNPs) [1].</p>Fórmula:C54H111N5O7Forma y color:SolidPeso molecular:942.49Anticancer agent 144
CAS:<p>Compound 144 (also known as Anticancer Agent 144) is a potent inhibitor of both PTPN2 and PTP1B, exhibiting IC50 values of less than 2.5 nM, making it suitable</p>Fórmula:C19H15BrF2N3O6PS2Pureza:98%Forma y color:SolidPeso molecular:594.3411-Hexadecenoic Acid
CAS:<p>11-Hexadecenoic acid, a monounsaturated fatty acid, comprises both 11-cis-hexadecenoic acid and 11-trans-hexadecenoic acid. These isoforms are present in ewe milk fat and their concentrations increase when the diet is supplemented with lipids from linseed, sunflower, olive, or fish oils. Additionally, 11-trans-hexadecenoic acid is found in intramuscular fat of both male and female foals. The product is a blend of the 11-cis and 11-trans forms. [Matreya, LLC. Catalog No. 1208]</p>Fórmula:C16H30O2Forma y color:SolidPeso molecular:254.41Biliverdin
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:582.65

