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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 8626 productos de "Metabolismo"

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  • 5-LOX/MAOs-IN-1

    CAS:
    <p>Compound 3, known as 5-LOX/MAOs-IN-1, acts as an inhibitor of 5-LOX/MAOs and is an effective free radical scavenger, displaying antioxidant characteristics. It has demonstrated neuroprotective effects in cell models damaged by oxidative stress and is capable of activating the neurogenesis microenvironment in adult mouse neural stem cells. This compound is utilized in research focused on neurodegenerative diseases.</p>
    Fórmula:C18H18N2O2
    Forma y color:Solid
    Peso molecular:294.35
  • 2R,4S-Sacubitril

    CAS:
    <p>2R,4S-Sacubitril (Sacubitril Enantiomer) is the impurity of Sacubitril which is a neprilysin inhibitor.</p>
    Fórmula:C24H28NO51Ca
    Pureza:98%
    Forma y color:Solid
    Peso molecular:430.49
  • BAY-179

    CAS:
    <p>BAY-179 is a potent, selective, species cross-reactive complex I inhibitor for the study of cancer.</p>
    Fórmula:C23H21N5OS
    Pureza:98.29%
    Forma y color:Solid
    Peso molecular:415.51
  • FXR/CES2 modulator 1

    CAS:
    <p>Compound LE-77, known as FXR/CES2 modulator 1, functions as a dual regulator that activates FXR and inhibits CES2. It effectively mitigates the intestinal toxicity of irinotecan.</p>
    Fórmula:C27H21Cl2NO5
    Forma y color:Solid
    Peso molecular:510.36
  • α-Amylase-IN-7

    CAS:
    <p>α-Amylase-IN-7 (Compound 6e) is an inhibitor of α-Amylase, with an IC50 of 40 μM, indicating its potency. This compound shows potential as an anti-diabetic medication.</p>
    Fórmula:C18H15ClN6O2S
    Peso molecular:414.87
  • Fonadelpar

    CAS:
    <p>Fonadelpar is an agonist of PPARδ. It also is used in the research of neuroparalytic keratopathy.</p>
    Fórmula:C25H23F3N2O4S
    Pureza:98%
    Forma y color:Solid
    Peso molecular:504.52
  • PF-00489791

    CAS:
    <p>PF-00489791 (PF4634817) is a long-acting PDE5 inhibitor with hypotensive activity for the study of diabetic nephropathy.</p>
    Fórmula:C20H28N8O4S
    Pureza:99.97%
    Forma y color:Solid
    Peso molecular:476.55
  • Etamicastat

    CAS:
    <p>Etamicastat can be used in the research of cardiovascular diseases.</p>
    Fórmula:C14H15F2N3OS
    Pureza:98%
    Forma y color:Solid
    Peso molecular:311.35
  • Lecufexor

    CAS:
    <p>Lecufexor is an agonist of the farnesoid X receptor (FXR).</p>
    Fórmula:C32H21Cl3N2O5
    Forma y color:Solid
    Peso molecular:619.88
  • SHP2 IN-1

    CAS:
    <p>SHP2 IN-1 is an allergic SHP2 (PTPN11) inhibitor(IC50 : 3 nM).</p>
    Fórmula:C18H22Cl2N6OS
    Pureza:98%
    Forma y color:Solid
    Peso molecular:441.38
  • GGACK

    CAS:
    <p>GGACK (H-Glu-Gly-Arg-CMK) is an irreversible substrate-like inhibitor of the serine protease urokinase-type plasminogen activator (uPA).</p>
    Fórmula:C14H25ClN6O5
    Peso molecular:392.84
  • Desmonomethylpromazine

    CAS:
    <p>Desmonomethylpromazine is a demethylated metabolite of Promazine that can penetrate the brain. It enters red blood cells and tissues via passive diffusion and is distributed in organs such as the lungs, liver, and kidneys in rats.</p>
    Fórmula:C16H18N2S
    Forma y color:Solid
    Peso molecular:270.39
  • DH376

    CAS:
    <p>DH376 inhibits DAGLα in a time and dose dependent manner in mouse brain. DH376 shows picomolar activity.</p>
    Fórmula:C31H28F2N4O3
    Forma y color:Solid
    Peso molecular:542.58
  • Gcase activator 2

    CAS:
    <p>Gcase activator 2 is a β-glucocerebrosidase activator that induces dimerization of GCase, increases lysosomal substrate metabolism.</p>
    Fórmula:C21H24N4O2
    Pureza:99.51% - 99.76%
    Forma y color:Solid
    Peso molecular:364.44
  • Calcipotriol Impurity C

    CAS:
    <p>Calcipotriol Impurity C is the impurity of Calcipotriol. Calcipotriol is a VDR-like receptors ligand.</p>
    Fórmula:C27H40O3
    Pureza:98%
    Forma y color:Solid
    Peso molecular:412.614
  • ent-8-iso-15(S)-Prostaglandin F2α

    CAS:
    <p>Isoprostanes are produced by the non-enzymatic, free radical peroxidation of phospholipid-esterified arachidonic acid.</p>
    Fórmula:C20H34O5
    Forma y color:Solid
    Peso molecular:354.48
  • LXRβ agonist-3

    CAS:
    <p>LXRβ agonist-3 is a potent and selective LXRβ (liver X receptor β) agonist (EC50: 0.095 μM).</p>
    Fórmula:C30H33N3O6S
    Forma y color:Solid
    Peso molecular:563.66
  • Keto lovastatin

    CAS:
    <p>Keto lovastatin is an impurity of lovastatin with antibacterial properties. Lovastatin is a cell-permeable HMG-CoA reductase (HMG-CoA reductase) inhibitor used to reduce cholesterol levels.</p>
    Fórmula:C24H34O6
    Forma y color:Solid
    Peso molecular:418.523
  • HIF-1/2α-IN-1


    <p>HIF-1/2α-IN-1, an orally active compound, functions as an inhibitor of HIF-2α.</p>
    Fórmula:C17H16N6O4
    Forma y color:Solid
    Peso molecular:368.35
  • α-Glucosidase-IN-17

    CAS:
    <p>α-Glucosidase-IN-17 (Compound 12B) is a potent and orally active inhibitor of α-glucosidase, demonstrating antidiabetic activity with an inhibitory</p>
    Fórmula:C30H27NO2S
    Forma y color:Solid
    Peso molecular:465.61