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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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  • Dendrogenin A
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    Dendrogenin A

    CAS:
    <p>Dendrogenin A (DDA) is a compound acting as a selective liver X receptor (LXR) modulator, cholesterol epoxide hydrolase inhibitor (Ki = 120 nM), and a metabolic</p>
    Fórmula:C32H55N3O2
    Forma y color:Solid
    Peso molecular:513.80

    Ref: TM-T83765

  • ICMT-IN-27
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    ICMT-IN-27

    CAS:
    <p>ICMT-IN-27, also known as compound 64, is an inhibitor of the enzyme ICMT, demonstrating potent activity with an IC50 value of 0.1 µM [1].</p>
    Fórmula:C22H28FNO2
    Forma y color:Solid
    Peso molecular:357.46

    Ref: TM-T82117

  • AR453588 hydrochloride
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    AR453588 hydrochloride

    CAS:
    <p>AR453588 hydrochloride is an orally bioavailable anti-diabetic glucokinase activator (EC50: 42 nM) with anti-hyperglycemic activity.</p>
    Fórmula:C25H26ClN7O2S2
    Pureza:98%
    Forma y color:Solid
    Peso molecular:556.1

    Ref: TM-T10362L

  • KD-026
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    KD-026

    CAS:
    <p>KD-026 (SLx 4090), a microsomal triglyceride transfer protein (MTP) inhibitor(IC50 = 8.0 nM), is used in type 2 diabetes studies.</p>
    Fórmula:C31H25F3N2O4
    Pureza:99.74%
    Forma y color:Solid
    Peso molecular:546.54

    Ref: TM-T27719

  • 17(S)-HpDHA
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    17(S)-HpDHA

    CAS:
    <p>17(S)-HpDHA, primarily produced by the 15-Lipoxygenase (LOX) isoenzymes h15-LOX-1 and h15-LOX-2 from docosahexaenoic acid (DHA), is a key regulator in epoxide synthesis through allosteric modulation. Additionally, it effectively inhibits platelet aggregation, demonstrating an EC50 of approximately 1 μM [1].</p>
    Fórmula:C22H32O4
    Forma y color:Solid
    Peso molecular:360.49

    Ref: TM-T84487

  • Cav 3.2 inhibitor 4
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    Cav 3.2 inhibitor 4

    CAS:
    <p>Cav 3.2 Inhibitor 4 (Compound 21) is a selective and potent inhibitor of the T-type calcium channel (Ca v 3.2), demonstrating peripheral restriction with an</p>
    Fórmula:C21H32Cl2N4O3
    Pureza:98%
    Forma y color:Solid
    Peso molecular:459.41

    Ref: TM-T79195

  • Perindopril acyl-β-D-glucuronide
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    Perindopril acyl-β-D-glucuronide

    CAS:
    <p>Perindopril acyl-β-D-glucuronide is a metabolite of the ACE inhibitor perindopril [1].</p>
    Fórmula:C25H40N2O11
    Pureza:98%
    Forma y color:Solid
    Peso molecular:544.59

    Ref: TM-T78136

  • Sampatrilat
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    Sampatrilat

    CAS:
    <p>Sampatrilat, an oral vasopeptidase inhibitor, more potently blocks C-domain ACE (Ki=13.8 nM) over N-domain (Ki=171.9 nM).</p>
    Fórmula:C26H40N4O9S
    Pureza:98%
    Forma y color:Solid
    Peso molecular:584.68

    Ref: TM-T16840

  • (S)-(-)-Bay-K-8644
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    (S)-(-)-Bay-K-8644

    CAS:
    <p>(S)-(-)-Bay-K-8644 ((S)-(-)-Bay K 8644) is an agonist of L-type Ca2+ channel and activates Ba2+ currents with an EC50 of 32 nM.</p>
    Fórmula:C16H15F3N2O4
    Pureza:98.28% - 99.37%
    Forma y color:Solid
    Peso molecular:356.3

    Ref: TM-TQ0144

  • ICMT-IN-39
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    ICMT-IN-39

    CAS:
    <p>ICMT-IN-39, also known as compound 18, functions as an inhibitor of ICMT with an IC50 value of 0.031 µM [1].</p>
    Fórmula:C22H29NO
    Forma y color:Solid
    Peso molecular:323.47

    Ref: TM-T82104

  • 3-Oxo Atorvastatin
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    3-Oxo Atorvastatin

    CAS:
    <p>3-Oxo Atorvastatin is an impurity of Atorvastatin. Atorvastatin is an HMG-CoA reductase inhibitor and has the ability to effectively decrease blood lipids.</p>
    Fórmula:C33H33FN2O5
    Pureza:98%
    Forma y color:Solid
    Peso molecular:556.62

    Ref: TM-T10120

  • GNE-6468
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    GNE-6468

    CAS:
    <p>GNE-6468 is a potent and selective agonist of RORγ(RORc) (EC50: 13 nM for HEK-293 cell).</p>
    Fórmula:C23H16ClN3O4
    Forma y color:Solid
    Peso molecular:433.84

    Ref: TM-T15404

  • Monoacylglycerol lipase inhibitor 1
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    Monoacylglycerol lipase inhibitor 1

    CAS:
    <p>Monoacylglycerol lipase inhibitor 1, also known as compound 13 [1], is a potent inhibitor of monoacylglycerol lipase.</p>
    Fórmula:C21H28N2O3
    Forma y color:Solid
    Peso molecular:356.46

    Ref: TM-T61294

  • Logo de CymitQuimica
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    hCAIX-IN-16

    CAS:
    hCAIX-IN-16 (Compound 12d), an inhibitor of hCA IX, exhibits inhibition constants (K i) of 190.0 nM for hCA IX and 187.9 nM for hCA XII.
    Fórmula:C20H20N8O2S
    Pureza:98%
    Forma y color:Solid
    Peso molecular:436.49

    Ref: TM-T73028

  • PDE7-IN-3
    Targetmol
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    PDE7-IN-3

    CAS:
    <p>PDE7-IN-3 (Example 2) serves as an inhibitor of phosphodiesterase PDE7 and exhibits potential analgesic properties.</p>
    Fórmula:C18H21ClN2O4
    Forma y color:Solid
    Peso molecular:364.82

    Ref: TM-T78559

  • H-0106 Dihydrochloride
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    H-0106 Dihydrochloride

    CAS:
    <p>H-0106 Dihydrochloride is an inhibitor of ROCK that acts by applying strong intraocular pressure (IOP)-lowering effects into the eyes of monkeys.</p>
    Fórmula:C16H22Cl3N3O2S
    Pureza:98%
    Forma y color:Solid
    Peso molecular:426.79

    Ref: TM-T25483

  • RB 101
    Targetmol
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    RB 101

    CAS:
    <p>RB 101 suppresses enkephalinase and aminopeptidases; biologically cleaved at disulfide to produce inhibitors of both aminopeptidase N and neutral endopeptidase.</p>
    Fórmula:C31H38N2O3S3
    Pureza:98%
    Forma y color:Solid
    Peso molecular:582.84

    Ref: TM-T26048

  • ICMT-IN-16
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    ICMT-IN-16

    CAS:
    <p>ICMT-IN-16 (compound 33) functions as an inhibitor of ICMT, demonstrating inhibitory concentration 50% (IC50) efficacy at 0.131 μM [1].</p>
    Fórmula:C23H32N2O
    Forma y color:Solid
    Peso molecular:352.51

    Ref: TM-T82129

  • YM17E
    Targetmol
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    YM17E

    CAS:
    <p>YM17E is an inhibitor of ACAT with IC50 of 44 nM in rabbit liver microsomes in vitro.</p>
    Fórmula:C40H56N6O2
    Pureza:99.29%
    Forma y color:Solid
    Peso molecular:652.91

    Ref: TM-T13373

  • Ionizable lipid-2
    Targetmol
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    Ionizable lipid-2

    CAS:
    <p>Ionizable Lipid-2 (Compound 1) serves as an ionizable lipid, essential for nucleic acid delivery and the construction of lipid nanoparticles (LNPs) [1].</p>
    Fórmula:C50H99NO7
    Forma y color:Solid
    Peso molecular:826.32

    Ref: TM-T84707