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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 8625 productos de "Metabolismo"

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  • 13(R)-HODE
    Targetmol
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    13(R)-HODE

    CAS:
    <p>13(R)-HODE, produced from linoleic acid, inhibits platelet aggregation (IC50=2.7μM) and is found in bovine endothelial cells.</p>
    Fórmula:C18H32O3
    Forma y color:Solid
    Peso molecular:296.44

    Ref: TM-T37973

  • Logo de CymitQuimica
    Targetmol
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    sEH inhibitor-2

    <p>SEH inhibitor-2 is an orally active sEH blocker (IC50=0.9 nM) with predicted 71.2-88.4% absorption, potentially aiding cardiovascular health.</p>
    Fórmula:C23H18N4O3
    Forma y color:Solid
    Peso molecular:398.41

    Ref: TM-T61894

  • hCAVII/IX-IN-1
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    hCAVII/IX-IN-1

    CAS:
    <p>hCAVII/IX-IN-1 (compound 4) functions as an inhibitor of hCAVII/IX, exhibiting Ki values of 56.5 nM and 38.2 nM, respectively. It is applicable in the field of cancer research.</p>
    Fórmula:C7H7N3O2S2
    Forma y color:Solid
    Peso molecular:229.279

    Ref: TM-T204621

  • Logo de CymitQuimica
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    sEH inhibitor-1

    <p>TCPU (sEH inhibitor-1) is a potent oral human sEH blocker with IC50s of 0.4 nM (human) and 5.3 nM (mouse).</p>
    Forma y color:Solid

    Ref: TM-T64291

  • PAT-347
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    PAT-347

    CAS:
    <p>PAT-347 is a potent inhibitor of Autotaxin, an enzyme linked to cell survival and diseases like cancer and fibrosis.</p>
    Fórmula:C28H21ClF2N2O3S
    Forma y color:Solid
    Peso molecular:538.99

    Ref: TM-T70275

  • Logo de CymitQuimica
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    EB-0150

    <p>EB-0150 inhibits ER α-Glu I/II (IC50: 0.73/0.0337 μM), is an N-substituted valerian with antiviral effects, and has drug discovery potential.</p>
    Fórmula:C19H30N6O7
    Forma y color:Solid
    Peso molecular:454.48

    Ref: TM-T62793

  • Logo de CymitQuimica
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    Oxythiamine diphosphate ammonium

    <p>Oxythiamin diphosphate ammonium is a potent inhibitor of transketolase (TK).</p>
    Forma y color:Solid

    Ref: TM-T64282

  • Ro 23-9358
    Targetmol
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    Ro 23-9358

    CAS:
    <p>Ro 23-9358 is a potent inhibitor of secretory phospholipase A2, exhibiting anti-inflammatory properties.</p>
    Fórmula:C30H51NO6
    Forma y color:Solid
    Peso molecular:521.729

    Ref: TM-T204941

  • NTPDase-IN-2
    Targetmol
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    NTPDase-IN-2

    CAS:
    <p>NTPDase-IN-2 inhibits h-NTPDase-2/-8 (IC50: 0.04, 2.27 µM), non-competitive for h-NTPDase-1/-2 (Km: 74 µM); useful in cancer, immune, bacterial research.</p>
    Fórmula:C24H20FN3OS2
    Forma y color:Solid
    Peso molecular:449.56

    Ref: TM-T62703

  • Logo de CymitQuimica
    Targetmol
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    hMAO-B/MB-COMT-IN-2

    <p>Dual inhibitor hMAO-B/MB-COMT-IN-2 targets hMAO-B (IC50: 4.27μM) &amp; MB-COMT (IC50: 2.69μM), aids in neurodegenerative research.</p>
    Fórmula:C17H18N2O3
    Forma y color:Solid
    Peso molecular:298.34

    Ref: TM-T60658

  • Dihydrokainic acid
    Targetmol
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    Dihydrokainic acid

    CAS:
    <p>EAAT2(GLT1)-selective non-transportable inhibitor of L-glutamate and L-aspartate uptake</p>
    Fórmula:C10H17NO4
    Pureza:98%
    Forma y color:Solid
    Peso molecular:215.25

    Ref: TM-T22722

  • 7-Hydroxyrisperidone
    Targetmol
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    7-Hydroxyrisperidone

    CAS:
    <p>7-Hydroxyrisperidone (7-RispOH) is a metabolite of Risperidone. Risperidone acts as a 5-HT2 receptor blocker, an inhibitor of P-glycoprotein (P-Glycoprotein), and an antagonist of the dopamine D2 receptor.</p>
    Fórmula:C23H27FN4O3
    Forma y color:Solid
    Peso molecular:426.484

    Ref: TM-TYD-01954

  • CB30865
    Targetmol
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    CB30865

    CAS:
    <p>CB30865 (ZM 242421) is a selective and highly effective nicotinamide phosphoribosyltransferase (Nampt) inhibitor with potential antitumor activity.</p>
    Fórmula:C26H22BrN5O2
    Pureza:99.04%
    Forma y color:Solid
    Peso molecular:516.39

    Ref: TM-T14882

  • Porphobilinogen
    Targetmol
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    Porphobilinogen

    CAS:
    <p>Porphobilinogen act as a phytotoxin, a metabotoxin, and a neurotoxin.</p>
    Fórmula:C10H14N2O4
    Pureza:98%
    Forma y color:Solid
    Peso molecular:226.23

    Ref: TM-T19130

  • Casein kinase 1δ-IN-18
    Targetmol
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    Casein kinase 1δ-IN-18

    CAS:
    <p>Casein kinase1δ-IN-18 (compound 660) is an inhibitor of casein kinase 1δ (CK1δ), which can be utilized for research in neurodegenerative diseases.</p>
    Fórmula:C16H12ClN3O2S2
    Forma y color:Solid
    Peso molecular:377.868

    Ref: TM-T204934

  • RORγt inverse agonist 34
    Targetmol
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    RORγt inverse agonist 34

    CAS:
    <p>RORγt inverse agonist 34 (compound 5a) is an inverse agonist for RORγt, exhibiting an IC50 of 0.094 μM for the inhibition of RORγt-LBD. This compound is utilized in psoriasis research.</p>
    Fórmula:C31H37N3O3S
    Forma y color:Solid
    Peso molecular:531.709

    Ref: TM-T204288

  • Logo de CymitQuimica
    Targetmol
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    Monoamine oxidase/Aromatase-IN-1

    <p>Compound 2q: Dual MAO/aromatase inhibitor; IC50: 39 nM (MAO-B), 31 nM (aromatase). Useful in neurological/breast cancer research.</p>
    Fórmula:C19H19N3O3S
    Forma y color:Solid
    Peso molecular:369.44

    Ref: TM-T61463

  • Logo de CymitQuimica
    Targetmol
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    PDHK-IN-5

    <p>PDHK-IN-5, potent PDHK2 (0.006 μM IC50) &amp; PDHK4 (0.0329 μM IC50) inhibitor, may be explored for cancer and diabetes treatment.</p>
    Fórmula:C30H31N5O2
    Forma y color:Solid
    Peso molecular:493.6

    Ref: TM-T63327

  • GSK864
    Targetmol
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    GSK864

    CAS:
    <p>GSK864 is an inhibitor of isocitrate dehydrogenase 1 (IDH1) mutant. GSK864 inhibits IDH1 mutants R132C, R132H, and R132G (IC50: 8.8, 15.2, and 16.6 nM).</p>
    Fórmula:C30H31FN6O4
    Pureza:97.07%
    Forma y color:Solid
    Peso molecular:558.6

    Ref: TM-T15442

  • RMGPa-IN-1
    Targetmol
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    RMGPa-IN-1

    CAS:
    <p>RMGPa-IN-1 (Compound 10C) is an inhibitor of rabbit muscle glycogen phosphorylase a (RMGPa), exhibiting an IC50 value of 82.5 μM. This compound holds potential for research in diabetes.</p>
    Fórmula:C33H54O4
    Forma y color:Solid
    Peso molecular:514.779

    Ref: TM-T206441