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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.

Subcategorías de "Metabolismo"

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Se han encontrado 8595 productos de "Metabolismo"

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  • Antiproliferative agent-13

    CAS:
    <p>Antiproliferative agent-13 is a compound with antiproliferative activity.</p>
    Fórmula:C20H18N2O6
    Pureza:99.723%
    Forma y color:Solid
    Peso molecular:382.37
  • Eflucimibe

    CAS:
    <p>Eflucimibe (L0081), an ACAT inhibitor, treats cardiovascular, endocrine, and metabolic diseases, and helps in atherosclerosis and hyperlipidemia research.</p>
    Fórmula:C29H43NO2S
    Pureza:99.17% - 99.43%
    Forma y color:Solid
    Peso molecular:469.72
  • ATX inhibitor 7

    CAS:
    <p>ATX inhibitor 7 is a autotaxin inhibitor and shows good oral exposure.</p>
    Fórmula:C21H22F3N7O2
    Forma y color:Solid
    Peso molecular:461.449
  • Burnettramic Acid A aglycone

    CAS:
    <p>Burnettramic acid A aglycone, from A. burnettii, has anticancer properties; cytotoxic to NS-1 cells (IC50 = 8.4 μg/ml), not to fibroblasts (&gt;100 μg/ml).</p>
    Fórmula:C35H61NO7
    Forma y color:Solid
    Peso molecular:607.873
  • SAICAR

    CAS:
    <p>SAICAR is an intermediate of de novo purine nucleotide biosynthesis, activates pyruvate kinase isoform M2 (PKM2) in an isozyme-selective manner (EC50: 0.3 mM).</p>
    Fórmula:C13H19N4O12P
    Pureza:98%
    Forma y color:Solid
    Peso molecular:454.28
  • α-Glucosidase-IN-60


    <p>α-Glucosidase-IN-60 (Compound 5k) acts as a competitive inhibitor of α-Glucosidase, with an IC50 of 10.8 μM.</p>
    Fórmula:C23H14N2O5
    Peso molecular:398.09027
  • Ritonavir metabolite

    CAS:
    <p>Ritonavir metabolite is a Ritonavir metabolite, which is a inhibitor of HIV protease.</p>
    Fórmula:C32H45N5O3S
    Pureza:98%
    Forma y color:Solid
    Peso molecular:579.80
  • SGK1-IN-3 hydrochloride


    <p>SGK1-IN-3 hydrochloride (compound 3a) is an efficacious, orally bioavailable SGK1 inhibitor. The serine/threonine kinase SGK1 acts as an activator of the β-catenin pathway and strongly stimulates cartilage degradation, being upregulated under genomic control in diseased osteoarthritic cartilage. SGK1-IN-3 hydrochloride holds potential for osteoarthritis research.</p>
    Fórmula:C23H21Cl3N6O3S
    Peso molecular:566.04614
  • Garcinone B

    CAS:
    <p>Garcinone B, a xanthone derivative naturally isolated from the pericarp of Mangosteen, serves as a potent inhibitor of ACE2 and Mpro, and is utilized in COVID-</p>
    Fórmula:C23H22O6
    Pureza:98%
    Forma y color:Solid
    Peso molecular:394.42
  • WVSAV


    <p>WVSAV is a ligand for the PDZ2 domain (tyrosine phosphatase) with a dissociation constant (Kd) of 111 μM. It is utilized in studies of protein-ligand interactions.</p>
    Fórmula:C27H40N6O7
    Forma y color:Solid
    Peso molecular:560.64
  • DSPE-PEG1000-pPB


    <p>DSPE-PEG1000-pPB is a PEG compound consisting of DSPE and a cyclic oligopeptide (pPB). The pPB component exhibits a strong binding affinity to PDGFRβ, which is overexpressed in activated hepatic stellate cells (HSC). DSPE-PEG1000-pPB is applicable for drug delivery.</p>
    Forma y color:Odour Solid
  • Casein Kinase Substrates 3

    CAS:
    <p>Casein Kinase Substrates 3 is a substrate of casein kinase.</p>
    Fórmula:C85H139N27O35S
    Pureza:98%
    Forma y color:Solid
    Peso molecular:2131.24
  • Lysylglutamic acid

    CAS:
    <p>Lysylglutamic acid is a dipeptide composed of the amino acids lysine (Lysine, Lys) and glutamic acid (Glutamic acid, Glu), with an inhibitory constant (Ki) of 1.3 mM for the membrane transport protein PEPT1.</p>
    Fórmula:C11H21N3O5
    Forma y color:Solid
    Peso molecular:275.3
  • Ilexoside O

    CAS:
    <p>Ilexoside O, a root-derived triterpene saponin, modestly blocks XOD with an IC50 of 53.05 μM.</p>
    Fórmula:C53H86O22
    Forma y color:Solid
    Peso molecular:1075.249
  • CNBCA


    <p>CNBCA, a selective and potent competitive inhibitor of the SHP2 enzyme, exhibits an IC50 value of 0.87 μM.</p>
    Fórmula:C26H34O5
    Forma y color:Solid
    Peso molecular:426.55
  • α-Amylase-IN-4


    <p>α-Amylase-IN-4 (Compd 10y) exhibits the highest level of amylase inhibition, demonstrating an IC50 value of 17.83 ± 0.14 μg/mL [1].</p>
    Forma y color:Odour Solid
  • Adefovir diphosphate 2TEA


    <p>Adefovir diphosphate 2TEA,a metabolite of Adefovir, an oral reverse transcriptase inhibitor with antiviral activity against herpes, hepatitis B, and HIV.</p>
    Fórmula:C20H43N7O7P2
    Pureza:98.33%
    Forma y color:Solid
    Peso molecular:555.55
  • LDHA-IN-8

    CAS:
    <p>LDHA-IN-8, an inhibitor, inhibits the proliferation of pancreatic and lung cancer cells, decreasing the intracellular lactate content and increasing ROS levels.</p>
    Fórmula:C15H14N4O2
    Pureza:99.73%
    Forma y color:Solid
    Peso molecular:282.3
  • 1,3-Dipalmitoleoyl-rac-glycerol

    CAS:
    <p>1,3-Dipalmitoleoyl-rac-glycerol: a diacylglycerol inhibiting yeast α-glucosidase over rat's (IC50s: 4.45 vs 9326.5 μM). Used to study membrane potentials.</p>
    Fórmula:C35H64O5
    Forma y color:Solid
    Peso molecular:564.892
  • C18:1 Ceramide (d18:1/18:1(9Z))

    CAS:
    <p>C18:1 Ceramide (d18:1/18:1(9Z)) is a ceramide, and C18:1-Ceramide levels are elevated in overweight and insulin-resistant , advanced ovarian cancer.</p>
    Fórmula:C36H69NO3
    Pureza:99.96%
    Forma y color:Solid
    Peso molecular:563.94