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Transferase

Transferase

Transferases are a large class of enzymes that catalyze the transfer of functional groups, such as methyl, glycosyl, and phosphate groups, from one molecule to another. Inhibitors of transferases are used to study a wide range of biological processes, including signal transduction, metabolism, and gene expression. These inhibitors are essential tools in research areas such as cancer, metabolic diseases, and epigenetics, where dysregulation of transferase activity is implicated. At CymitQuimica, we offer a comprehensive selection of transferase inhibitors to support your research in enzymology, cell signaling, and disease mechanisms.

Found 30 products of "Transferase"

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  • Cycloleucine

    CAS:
    <p>Cycloleucine is an antagonist of NMDA receptor associated glycine receptor with a Ki of 600 μM.</p>
    Formula:C6H11NO2
    Purity:99.90%
    Color and Shape:Solid
    Molecular weight:129.16
  • Opicapone

    CAS:
    <p>Opicapone (BIA 9-1067), a potent COMT inhibitor for Parkinson's studies, lowers cell ATP (IC50: 98 μM).</p>
    Formula:C15H10Cl2N4O6
    Purity:98.17% - 99.36%
    Color and Shape:Solid
    Molecular weight:413.17
  • Sinbaglustat

    CAS:
    <p>Sinbaglustat (OGT2378), an oral N-alkyl iminosugar, inhibits GCS/GBA2 and treats lysosomal storage and neurodegenerative disorders.</p>
    Formula:C11H23NO4
    Purity:99.93%
    Color and Shape:Solid
    Molecular weight:233.3
  • Histamine glutarimide

    CAS:
    <p>Histamine glutarimide is a novel QPCT inhibitor that targets inflammatory processes like eosinophil migration, showing anti-asthmatic effects in animal models.</p>
    Formula:C10H13N3O2
    Purity:99.79%
    Color and Shape:Solid
    Molecular weight:207.23
  • FUT8-IN-1


    <p>FUT8-IN-1 (Compound 37) is an inhibitor of α-1,6-fucosyltransferase (FUT8), with a dissociation constant (KD) of 49 nM and an IC50 around 50 µM. In the presence of FUT8, FUT8-IN-1 forms a highly active naphthoquinone imine intermediate, thereby inhibiting FUT8's enzymatic activity.</p>
    Formula:C23H25ClN2O
    Color and Shape:Solid
    Molecular weight:380.91
  • β-1,4-GALT1-IN-1


    <p>β-1,4-GALT1-IN-1 (Compound 6) is a β-1,4-GALT1 inhibitor with an IC50 value of 6.2 μM. It is applicable in studying various pathological conditions, including cancer, autoimmune diseases, and viral infections.</p>
    Formula:C29H23NO10
    Color and Shape:Solid
    Molecular weight:545.494
  • ST6 Sialyltransferase 5


    <p>ST6Sialyltransferase5 (EC:2.4.3.3, ST6GALNAC5, SIAT7E, ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 5) transfers sialic acid to N-acetylgalactosamine (GalNAc) residues. It may serve as a biomarker in cervical screening samples.</p>
  • L-739750 2HCl


    <p>L-739750 2HCl is a potent inhibitor of peptidomimetic farnesyltransferase, a novel pseudopeptide mimetic with potential anticancer activity.</p>
    Formula:C23H41Cl2N3O6S2
    Purity:98.69% - 99.16%
    Color and Shape:Soild
    Molecular weight:590.62
  • Tipifarnib

    CAS:
    <p>Tipifarnib (IND 58359), a quinolinone, inhibits farnesyl transferase, blocks Ras activation, arrests cell growth, and curbs angiogenesis.</p>
    Formula:C27H22Cl2N4O
    Purity:97.1% - 99.22%
    Color and Shape:Off-White To Pale Beige Solid
    Molecular weight:489.4
  • Ibiglustat

    CAS:
    <p>Ibiglustat (GZ402671) inhibits Glucosylceramide synthase, may treat Fabry disease by preventing GL-3 synthesis.</p>
    Formula:C20H24FN3O2S
    Purity:97.97% - 98.81%
    Color and Shape:Solid
    Molecular weight:389.49
  • Entacapone

    CAS:
    <p>Entacapone (OR-611) is a selective and reversible inhibitor of catechol-O-methyltransferase (COMT).</p>
    Formula:C14H15N3O5
    Purity:98.80% - >99.99%
    Color and Shape:Yellow Crystalline Solid
    Molecular weight:305.29
  • Tipifarnib (S enantiomer)

    CAS:
    <p>Tipifarnib S enantiomer ((S)-(-)-R-115777) is the S-enantiomer of Tipifarnib. Tipifarnib is a potent and specific farnesyltransferase inhibitor (IC50: 0.6 nM).</p>
    Formula:C27H22Cl2N4O
    Purity:99.05%
    Color and Shape:Solid
    Molecular weight:489.4
  • PD 128042

    CAS:
    <p>PD 128042 (CI 976) is a potent orally active and selective ACAT inhibitor(IC50: 73 nM) and a potent lysophospholipid acyltransferase(LPAT) inhibitor.</p>
    Formula:C23H39NO4
    Purity:99.79%
    Color and Shape:Solid
    Molecular weight:393.56
  • CP-609754

    CAS:
    <p>CP-609754 shows selective inhibition of farnesyltransferase.</p>
    Formula:C29H22ClN3O2
    Purity:99.04% - 99.86%
    Color and Shape:Solid
    Molecular weight:479.96
  • Nitecapone

    CAS:
    <p>Nitecapone is a reversible inhibitor of S-COMT (IC50 values of 300 nM in rat liver)</p>
    Formula:C12H11NO6
    Purity:98.39%
    Color and Shape:Solid
    Molecular weight:265.22
  • Ervogastat

    CAS:
    <p>Ervogastat (PF-06865571) is a potent and well-tolerated diacylglycerol acyltransferase 2 inhibitor.</p>
    Formula:C21H21N5O4
    Purity:99.97%
    Color and Shape:Solid
    Molecular weight:407.42
  • 3-O-Methyltolcapone

    CAS:
    <p>3-O-Methyltolcapone (Ro 40-7591) is a metabolite of Tolcapone which is a potent COMT inhibitor.</p>
    Formula:C15H13NO5
    Purity:98%
    Color and Shape:Solid
    Molecular weight:287.27
  • AMP-Deoxynojirimycin

    CAS:
    <p>AMP-Deoxynojirimycin (AMP-DNM) is a ceramide glucosyltransferase and GCase 2 inhibitor for the study of Parkinson's and diabetes.</p>
    Formula:C22H39NO5
    Purity:>99.99%
    Color and Shape:Solid
    Molecular weight:397.55
  • Lucerastat

    CAS:
    <p>Lucerastat(NBDGJ) is an orally available inhibitor of GCS for Fabry disease by reducing harmful substrates.. GCS is a key enzyme in sphingolipid synthesiss.</p>
    Formula:C10H21NO4
    Purity:98%
    Color and Shape:Solid
    Molecular weight:219.28
  • P-3FAX-Neu5Ac

    CAS:
    <p>P-3FAX-Neu5Ac is a sialic acid analog and a sialyltransferase inhibitor.</p>
    Formula:C22H30FNO14
    Purity:97.08%
    Color and Shape:Solid
    Molecular weight:551.47