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Metabolismo

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.

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Se han encontrado 8628 productos de "Metabolismo"

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  • γ-Glutamylserine TFA


    <p>γ-Glutamylserine TFA (γ-Glu-Ser TFA) serves as a calcium receptor activator and is utilized in research focused on Parkinson's disease, diabetes, and obesity [1</p>
    Fórmula:C10H15F3N2O8
    Pureza:98%
    Forma y color:Soild
    Peso molecular:348.23
  • FABP4-IN-2


    <p>FABP4-IN-2 (Compd 10g), a selective and orally active FABP4 inhibitor, exhibits K i values of 0.51 μM for FABP4 and 33.01 μM for FABP3, demonstrating its</p>
    Fórmula:C22H14ClF3O3
    Pureza:98%
    Forma y color:Solid
    Peso molecular:418.79
  • DSPE-PEG1000-MPG


    <p>DSPE-PEG1000-MPG is a PEG compound composed of DSPE and the peptide carrier (MPG). MPG is derived from the nuclear localization sequence (NLS) of the SV40 large T antigen and the fusion peptide domain of HIV-1 gp41. MPG efficiently delivers short oligonucleotides into cells, operating independently of endosomal pathways.</p>
    Forma y color:Odour Solid
  • α-Glucosidase-IN-33


    <p>α-Glucosidase-IN-33 (compound 7c), with an IC50 of 2.39 μM, is a potent inhibitor of α-glucosidase and is relevant in research on type 2 diabetes and</p>
    Fórmula:C26H19F3N2O4
    Pureza:98%
    Forma y color:Solid
    Peso molecular:480.44
  • Seco Rapamycin

    CAS:
    <p>Seco Rapamycin, a ring-opened Rapamycin derivative, does not affect mTOR function.</p>
    Fórmula:C51H79NO13
    Forma y color:Solid
    Peso molecular:914.187
  • ThioLox

    CAS:
    <p>ThioLox, a 15-LOX-1 inhibitor (IC50: 12 μM), has anti-inflammatory, neuroprotective benefits, and guards against glutamate toxicity.</p>
    Fórmula:C15H18N2OS
    Pureza:99.98%
    Forma y color:Soild
    Peso molecular:274.38
  • Cavosonstat

    CAS:
    <p>Cavosonstat (N91115) is an oral GSNOR inhibitor aiding CFTR in cystic fibrosis.</p>
    Fórmula:C16H10ClNO3
    Pureza:98.91%
    Forma y color:Solid
    Peso molecular:299.71
  • Cerebroside C

    CAS:
    <p>Cerebroside C, a fungal glycosphingolipid from M. grisea, stimulates phytoalexin in rice and enhances wheat germination and growth at 4°C.</p>
    Fórmula:C43H79NO9
    Forma y color:Solid
    Peso molecular:754.09
  • Thymus peptide C

    CAS:
    <p>Thymus peptide C, a hormonal drug derived from the thymus glands of young calves, acts as a substitute for the physiological functions of the thymus.</p>
    Fórmula:NA
    Pureza:98%
    Forma y color:Solid
    Peso molecular:N/A
  • PF-07238025


    <p>PF-07238025, a potent branched-chain ketoacid dehydrogenase kinase (BDK) inhibitor with an EC50 of 19 nM, enhances the stability of the BDK-BCKDH core E2</p>
    Fórmula:C19H18N2O3S
    Pureza:98%
    Forma y color:Solid
    Peso molecular:354.42
  • Alanine aminotransferase

    CAS:
    <p>Alanine aminotransferase (ALT), a pyridoxal-dependent enzyme, catalyzes the reversible interconversion of L-alanine and 2-oxoglutarate into pyruvate and L-</p>
    Pureza:98%
    Forma y color:Solid
  • Mevinolinic acid

    CAS:
    <p>Mevinolinic acid is an active metabolite of Lovastatin. Lovastatin is an HMG-CoA reductase inhibitor.</p>
    Fórmula:C24H38O6
    Pureza:98%
    Forma y color:Solid
    Peso molecular:422.562
  • hCA XII-IN-6


    <p>Compound 4d, known as hCA XII-IN-6, is a potent inhibitor of human carbonic anhydrase XII (hCA XII) with a Ki value of 84.2 nM and exhibits anti-proliferative</p>
    Fórmula:C11H9N5O3S2
    Pureza:98%
    Forma y color:Solid
    Peso molecular:323.35
  • IDO1-IN-23


    <p>IDO1-IN-23 (compound 41) is a potent inhibitor of human indoleamine 2,3-dioxygenase 1 (IDO1), exhibiting an IC50 of 13 μM [1].</p>
    Pureza:98%
    Forma y color:Odour Solid
  • HIF-1α-IN-6


    <p>HIF-1α-IN-6 (compound 3s) is a potent inhibitor of HIF-1α, demonstrating IC50 values of 0.6 nM and 53.3 nM in MiaPaCa-2 and MDA-MB-231 cells, respectively.</p>
    Pureza:98%
    Forma y color:Odour Solid
  • Aminopeptidase N inhibitor 2


    <p>AminopeptidaseN inhibitor 2 is an APN inhibitor (IC50: 4.3 μM) with antitumor properties.</p>
    Fórmula:C12H16F2N2O4S
    Forma y color:Solid
    Peso molecular:322.07988
  • Larsucosterol sodium

    CAS:
    <p>Larsucosterol sodium: a liver-derived cholesterol byproduct; modulates lipid synthesis, inflammation, and cell death regulation.</p>
    Fórmula:C27H46NaO5S
    Forma y color:Solid
    Peso molecular:505.71
  • Maximiscin

    CAS:
    <p>Maximiscin, a metabolite derived from fungi, causes DNA damage and exhibits selective cytotoxic activity towards a specific subtype of triple-negative breast</p>
    Fórmula:C23H31NO8
    Forma y color:Solid
    Peso molecular:449.49
  • Allotetrahydrocortisol

    CAS:
    <p>Allotetrahydrocortisol (5a-Tetrahydrocortisol) is a metabolite of Cortisol. Cortisol is the main glucocorticoid in human.</p>
    Fórmula:C21H34O5
    Pureza:98%
    Forma y color:Solid
    Peso molecular:366.49
  • D-Pro-Phe-Arg-Chloromethylketone

    CAS:
    D-Pro-Phe-Arg-Chloromethylketone, an inhibitor of coagulation factor XII and plasma kallikrein, is significant in the regulation of thrombosis and inflammation
    Fórmula:C21H31ClN6O3
    Pureza:98%
    Forma y color:Solid
    Peso molecular:450.96