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Metabolism

Metabolism

Metabolism inhibitors are compounds that interfere with metabolic pathways, altering the production and utilization of energy within cells. These inhibitors are used to study the regulation of metabolism, the role of metabolic pathways in diseases like cancer and diabetes, and to develop new therapeutic strategies. Metabolism inhibitors can target various enzymes and processes involved in glycolysis, fatty acid oxidation, and other metabolic functions. At CymitQuimica, we offer a wide range of high-quality metabolism inhibitors to support your research in biochemistry, metabolic disorders, and drug development.

Subcategories of "Metabolism"

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Found 9166 products of "Metabolism"

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  • LTA4H-IN-3

    CAS:
    LTA4H-IN-3 (compound 9) functions as an inhibitor of LTA4H, demonstrating an IC50 of 28 nM [1].
    Formula:C17H15ClN4O3
    Color and Shape:Solid
    Molecular weight:358.78

    Ref: TM-T86828

    10mg
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    50mg
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  • Thioquinapiperifil dihydrochloride

    CAS:
    Thioquinapiperifil dihydrochloride is a potent, selective PDE-5 inhibitor (IC50: 0.074 nM) for research.
    Formula:C24H29ClN6OS
    Purity:99.81%
    Color and Shape:Solid
    Molecular weight:485.05

    Ref: TM-T9773

    1mg
    58.00€
    5mg
    130.00€
    10mg
    187.00€
    25mg
    304.00€
    50mg
    393.00€
    100mg
    552.00€
    200mg
    725.00€
    1mL*10mM (DMSO)
    148.00€
  • IDO antagonist-1

    CAS:
    IDO antagonist-1 (compound 163), an IDO antagonist, effectively inhibits the growth of pancreatic adenocarcinoma cells in C57BL/6 mice [1].
    Formula:C39H53N7O5
    Color and Shape:Solid
    Molecular weight:699.88

    Ref: TM-T86703

    10mg
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    50mg
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  • Lecufexor

    CAS:
    Lecufexor is an agonist of the farnesoid X receptor (FXR).
    Formula:C32H21Cl3N2O5
    Color and Shape:Solid
    Molecular weight:619.88

    Ref: TM-T201138

    25mg
    2,108.00€
    50mg
    2,768.00€
    100mg
    3,715.00€
  • UGT1A1-IN-1

    CAS:
    UGT1A1-IN-1 (compound 2) acts as a non-competitive inhibitor of UGT1A1, effectively inhibiting the 1-O-glucuronidation process mediated by UGT1A1 with a Ki value of 5.02 μM. This compound binds to the same ligand-binding site on UGT1A1 as bilirubin and additionally functions as a 'turn-on' fluorescent probe substrate for UGT1A1 [1].
    Formula:C22H19NO3
    Color and Shape:Solid
    Molecular weight:345.39

    Ref: TM-T87592

    10mg
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  • Inosine 5′-diphosphate sodium

    CAS:
    Inosine 5'-diphosphate sodium, a purine ribonucleoside diphosphate with inosine as its nucleobase, plays a role in intracellular energy metabolism and signal transduction processes.
    Formula:C10H13N4Na3O12P2
    Color and Shape:Solid
    Molecular weight:512.15

    Ref: TM-T201310

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  • EC33

    CAS:
    EC33, a selective aminopeptidase A (APA) inhibitor, blocks the pressor response of exogenous Ang II and does not cross the blood-brain barrier, making it a potential candidate for salt-dependent hypertension research [1].
    Formula:C4H11NO3S2
    Color and Shape:Solid
    Molecular weight:185.27

    Ref: TM-T86337

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    50mg
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  • MAGL-IN-15

    CAS:
    MAGL-IN-15 (Compound 6), a MAGL inhibitor, holds potential for research into diseases and disorders associated with the regulation of endocannabinoid system signaling activities [1].
    Formula:C16H16F6N4O3
    Color and Shape:Solid
    Molecular weight:426.31

    Ref: TM-T86853

    10mg
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    50mg
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  • ABHD antagonist 1

    CAS:
    ABHD antagonist 1 is an inhibitor of ABHD6 (α/β-Hydrolase domain containing 6), involved in modulating biochemical pathways affected by ABHD6, thereby influencing cell function and inflammatory responses. This compound is applicable for research in fields such as pain, neurological disorders, inflammatory diseases, autoimmune diseases, metabolic disorders, and cancer.
    Formula:C19H20BrN3O3S
    Color and Shape:Solid
    Molecular weight:450.35

    Ref: TM-T88145

    25mg
    2,015.00€
    50mg
    2,642.00€
    100mg
    3,515.00€
  • Nampt activator-4

    CAS:
    Nampt activator-4, a positive allosteric modulator (N-PAM) of nicotinamide phosphoribosyltransferase (NAMPT), has an EC50 of 0.058 μM and can enhance nicotinamide adenine dinucleotide (NAD+) levels in cells [1].
    Formula:C26H22F3N7OS
    Color and Shape:Solid
    Molecular weight:537.56

    Ref: TM-T86957

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  • O-Desmethyl Brinzolamide hydrochloride

    CAS:
    O-Desmethyl Brinzolamide hydrochloride (compound 6a), a potent metabolite derived from Brinzolamide, serves as a carbonic anhydrase (CA) inhibitor. It exhibits a dissociation constant (Kd) of 0.136 nM for CA II and an inhibitory concentration (IC50) of 165 nM for CA IV [1].
    Formula:C11H20ClN3O5S3
    Color and Shape:Solid
    Molecular weight:405.94

    Ref: TM-T87055

    10mg
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    50mg
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  • Fmoc-NH-PEG6-alcohol

    CAS:
    Fmoc-NH-PEG6-alcohol, a cleavable ADC linker, is employed in the synthesis of antibody-drug conjugates (ADCs) [1].
    Formula:C27H37NO8
    Color and Shape:Solid
    Molecular weight:503.58

    Ref: TM-T86468

    10mg
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    50mg
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  • Lapaquistat

    CAS:
    Lapaquistat: active TAK-475 metabolite; reduces cholesterol synthesis and statin myotoxicity.
    Formula:C31H39ClN2O8
    Purity:98%
    Color and Shape:Solid
    Molecular weight:603.1

    Ref: TM-T15710

    25mg
    5,400.00€
    50mg
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    100mg
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  • E234G HYPE-IN-1

    CAS:
    Compound I2.10 (E234G HYPE-IN-1) functions as an AMPylase inhibitor and exhibits low cytotoxicity toward human cell lines [1].
    Formula:C14H9N5O2
    Color and Shape:Solid
    Molecular weight:279.25

    Ref: TM-T86314

    10mg
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    50mg
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  • D-Citrulline

    CAS:
    D-Citrulline (H-D-Cit-OH), a stereoisomer of L-citrulline, effectively reduces cardiac contractile dysfunction caused by polymorphonuclear leukocyte (PMN) in isolated perfused rat hearts undergoing ischemia/reperfusion. This protective effect is mediated through a non-NO-mediated mechanism.
    Formula:C6H13N3O3
    Color and Shape:Solid
    Molecular weight:175.19

    Ref: TM-T200340

    10mg
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    50mg
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  • Sulclamide

    CAS:
    Sulclamide, a sulfamoylbenzoic acid derivative, exhibits diuretic activity and functions as an inhibitor of carbonic anhydrase [1].
    Formula:C7H7ClN2O3S
    Color and Shape:Solid
    Molecular weight:234.66

    Ref: TM-T87453

    10mg
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    50mg
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  • DDO-3733

    CAS:
    DDO-3733 is a conformational activator of Protein Phosphatase 5 (PP5) that functions independently of TRP, facilitating the dephosphorylation of downstream substrates.
    Formula:C10H6F2N2OS
    Color and Shape:Solid
    Molecular weight:240.23

    Ref: TM-T200216

    25mg
    1,458.00€
    50mg
    1,839.00€
    100mg
    2,322.00€
  • HSD17B13-IN-19

    CAS:
    HSD17B13-IN-19 (compound 16) acts as a potent inhibitor of hydroxysteroid 17β-dehydrogenase 13 (HSD17B13), exhibiting IC50 values under 0.1 μM and under 1 μM when using estradiol and Leukotriene B3 as substrates, respectively. This compound is crucial in the treatment of nonalcoholic fatty liver diseases (NAFLDs), such as nonalcoholic steatohepatitis (NASH) [1].
    Formula:C23H23FN2O4S
    Color and Shape:Solid
    Molecular weight:442.5

    Ref: TM-T86609

    10mg
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    50mg
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  • Homodestcardin

    CAS:
    Homodestcardin: cyclic depsipeptide from T. roseum with immunosuppressant properties; inhibits mouse T cell proliferation.
    Formula:C32H55N5O7
    Color and Shape:Solid
    Molecular weight:621.81

    Ref: TM-T68351

    25mg
    2,313.00€
    50mg
    3,042.00€
    100mg
    4,140.00€
  • Carbonic anhydrase inhibitor 8


    R-13, a carbonic anhydrase inhibitor, has Ki of 60.7 nM (hCA I), 320.7 nM (hCA II), and 2298 nM (hCA IV).
    Formula:C20H25N3O4S
    Color and Shape:Solid
    Molecular weight:403.5

    Ref: TM-T61980

    25mg
    1,369.00€
    50mg
    1,783.00€
    100mg
    2,250.00€