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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 8628 productos de "Metabolismo"

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  • APP-018

    CAS:
    <p>APP-018 (D-4F) is an 18 D-amino acid peptide that mimics apolipoprotein A-I (apoA-I). It enhances the anti-inflammatory properties of high-density lipoprotein (HDL) and is applicable in cardiovascular disease research.</p>
    Fórmula:C114H156N24O28
    Forma y color:Solid
    Peso molecular:2310.6
  • Ercalcidiol

    CAS:
    <p>Ercalcidiol is a metabolite of vitamin D2 and can be used in monitoring vitamin D therapy.</p>
    Fórmula:C28H44O2
    Pureza:99.62%
    Forma y color:Solid
    Peso molecular:412.65
  • 3-Hydroxyanisole

    CAS:
    3-Hydroxyanisole has inhibitory activity against MAO-A (IC50 = 24 ± 2.8 μM) and can be used to study neurological and psychiatric diseases.
    Fórmula:C7H8O2
    Pureza:98.96%
    Forma y color:Clear Pink To Red Liquid With The Odor Of Phenol And Carmel
    Peso molecular:124.14
  • 11-Hydroxy cannabinol

    CAS:
    <p>11-Hydroxy cannabinol (Compound 5b) is an active metabolite of cannabinol.</p>
    Fórmula:C21H26O3
    Forma y color:Solid
    Peso molecular:326.43
  • cMCoFx1

    CAS:
    <p>cMCoFx1 is an effective and selective FXIIa cyclic peptide inhibitor. It exhibits high binding affinity for FXIIa (KD: 900 pM) and potent inhibitory activity (Ki: 370 pM). cMCoFx1 effectively suppresses the intrinsic coagulation pathway, demonstrates high stability in serum, and shows no cytotoxicity.</p>
    Fórmula:C146H232N52O44S6
    Forma y color:Solid
    Peso molecular:3612.12
  • BMT-124110 Formate


    <p>BMT-124110 Formate is a selective AAK1 inhibitor (IC50: 0.9 nM) with anti-injury sensory activity.BMT-124110 Formate inhibits the BMP-2-inducible protein kinase</p>
    Fórmula:C22H20N2O2
    Pureza:99.52%
    Forma y color:Soild
    Peso molecular:344.41
  • ZG-2305


    <p>ZG-2305 is an effective, selective, and orally active inhibitor of FIH (factor inhibiting hypoxia-inducible factor (FIH)), with Ki values of 79.6 nM for FIH and 2786 nM for PHD2. This compound enhances the expression of the EGLN3 gene, reduces cellular triglyceride levels, and decreases lipid accumulation. ZG-2305 holds potential for research into obesity and fatty liver disease.</p>
    Fórmula:C17H11Cl2N3O5
    Forma y color:Solid
    Peso molecular:408.19
  • 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
  • Leucomyosuppressin

    CAS:
    <p>Leucomyosuppressin, isolated from head extracts of the cockroach Leucophaea maderae, inhibits evoked transmitter release at the mealworm neuromuscular junction.</p>
    Fórmula:C59H84N16O15
    Pureza:98%
    Forma y color:Solid
    Peso molecular:1257.418
  • PTP1B-IN-14

    CAS:
    <p>PTP1B-IN-14 is a selective inhibitor of Protein Tyrosine Phosphatase 1B (PTP1B) that targets the allosteric site, exhibiting an inhibitory concentration (IC50)</p>
    Fórmula:C27H19N5O3S4
    Forma y color:Solid
    Peso molecular:589.73
  • TPT-004


    <p>TPT-004, a TPH inhibitor, exhibits superior pharmacokinetic and pharmacodynamic properties, and demonstrates efficacy in preclinical models for attenuating</p>
    Forma y color:Odour Solid
  • DPPD-Q

    CAS:
    <p>DPPD-Q, an antioxidant and an oxidative derivative of substituted p-phenylenediamine (DPPD), is identified in tire wear particles, rubber debris, particulate matter 2.5 (PM2.5), and wastewater influents and effluents. At a concentration of 5 µM, DPPD-Q inhibits soybean urease by 91.4%.</p>
    Fórmula:C18H14N2O2
    Forma y color:Solid
    Peso molecular:290.32
  • CUDA

    CAS:
    <p>CUDA is an effective soluble cyclohydrolase inhibitor with IC50 of 11.1 nM and 112 nM for mouse sEH and human sEH, respectively.</p>
    Fórmula:C19H36N2O3
    Pureza:97.585%
    Forma y color:Solid
    Peso molecular:340.5
  • HMG-CoA Reductase-IN-1


    <p>HMG-CoA Reductase-IN-1 is an inhibitor of HMG-CoA reductase, demonstrating strong inhibitory activity on HMGR and affinity for OATP1B1, with pIC50 and pKm</p>
    Fórmula:C27H29N3O7
    Forma y color:Solid
    Peso molecular:507.54
  • BAY 2666605

    CAS:
    <p>BAY 2666605 is an orally active inhibitor of PDE3A and PDE3B with IC50s of 87 nM and 50 nM, respectively. BAY 2666605 has anticancer effects.</p>
    Fórmula:C17H12F4N2O2
    Pureza:99.81%
    Forma y color:Solid
    Peso molecular:352.28
  • HIF-1 α (556-574)

    CAS:
    <p>HIF-1 alpha (556-574) is a 19-mer fragment vital for gene expression in low oxygen; it binds VHL with critical proline 564 for stability.</p>
    Fórmula:C101H150D2N20O34S2
    Pureza:98%
    Forma y color:Solid
    Peso molecular:2254.6
  • O-desmethyl Mebeverine acid

    CAS:
    <p>O-desmethyl Mebeverine acid is a metabolite of Mebeverine.</p>
    Fórmula:C15H23NO3
    Pureza:98%
    Forma y color:Solid
    Peso molecular:265.35
  • TMP-778

    CAS:
    TMP-778 is a selective inverse agonist of RORγt.
    Fórmula:C31H30N2O4
    Pureza:99.68%
    Forma y color:Solid
    Peso molecular:494.58
  • Adaptaquin

    CAS:
    <p>Adaptaquin is an inhibitor of the hypoxia-inducing factor prolyl hydroxylase (HIF-PH) [1] [2].</p>
    Fórmula:C21H16ClN3O2
    Pureza:99.75%
    Forma y color:Solid
    Peso molecular:377.82
  • N-Desmethyl Bendamustine

    CAS:
    <p>N-DesmethylBendamustine is a metabolite of Bendamustine. It exerts cytotoxic effects on various lymphoma cell lines and peripheral blood lymphocytes.</p>
    Fórmula:C15H19Cl2N3O2
    Forma y color:Solid
    Peso molecular:344.24