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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 42 products for "Transferase".

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  • CP-609754

    CAS:
    CP-609754 shows selective inhibition of farnesyltransferase.
    Formula:C29H22ClN3O2
    Purity:99.86% - 99.87%
    Color and Shape:Solid
    Molecular weight:479.957
  • Tipifarnib

    CAS:
    Tipifarnib (IND 58359), a quinolinone, inhibits farnesyl transferase, blocks Ras activation, arrests cell growth, and curbs angiogenesis.
    Formula:C27H22Cl2N4O
    Purity:97.1% - 99.94%
    Color and Shape:Off-White To Pale Beige Solid
    Molecular weight:489.396
  • 3-O-Methyltolcapone

    CAS:
    3-O-Methyltolcapone (Ro 40-7591) is a metabolite of Tolcapone which is a potent COMT inhibitor.
    Formula:C15H13NO5
    Purity:98%
    Color and Shape:Solid
    Molecular weight:287.2674
  • FUT8-IN-1


    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.
    Formula:C23H25ClN2O
    Color and Shape:Solid
    Molecular weight:380.91
  • Lith-O-Asp

    CAS:
    Lith-O-Asp is a sialyltransferase inhibitor; Ki=1.3 μM; reduces sialylation; inhibits cancer cell invasion; metastasis research.
    Formula:C28H45NO6
    Color and Shape:White Solid
    Molecular weight:491.66
  • Lucerastat

    CAS:
    Lucerastat(NBDGJ) is an orally available inhibitor of GCS for Fabry disease by reducing harmful substrates.. GCS is a key enzyme in sphingolipid synthesiss.
    Formula:C10H21NO4
    Purity:98%
    Color and Shape:White Solid
    Molecular weight:219.278
  • P-3FAX-Neu5Ac

    CAS:
    P-3FAX-Neu5Ac is a sialic acid analog and a sialyltransferase inhibitor.
    Formula:C22H30FNO14
    Purity:97.08%
    Color and Shape:White Solid
    Molecular weight:551.47
  • Prenyl-IN-1

    CAS:
    Prenyl-IN-1 inhibits prenylation selectively, counters oxidative stress in Parkinson's.
    Formula:C28H24ClN5O2
    Purity:>99.99%
    Color and Shape:Solid
    Molecular weight:497.98
  • PDMP hydrochloride

    CAS:
    PDMP, a glucosylceramide synthase inhibitor with 4 stereoisomers, acts at 0.8μM; D-threo enantiomer also blocks lactosylceramide synthesis.
    Formula:C23H39ClN2O3
    Color and Shape:Solid
    Molecular weight:427.03
  • DGAT1-IN-3

    CAS:
    DGAT1-IN-3 is an orally active DGAT-1 inhibitor (IC₅₀: 38 nM human, 120 nM rat) for obesity and metabolic syndrome research.
    Formula:C20H19F3N4O3
    Purity:99.83%
    Color and Shape:Solid
    Molecular weight:420.3851
  • EBU-141


    EBU-141 is a human monoclonal antibody (mAb) targeting CD75/ST6GAL1, suitable for research in B-cell lymphoma and multiple myeloma.
  • Ibiglustat (L-Malic acid)

    CAS:
    Ibiglustat (L-Malic acid) (Ibiglustat L-Malic acid) is a selective, brain-penetrant, and allosteric inhibitor of glucosylceramide synthase.
    Formula:C24H30FN3O7S
    Purity:99.54%
    Color and Shape:Solid
    Molecular weight:523.574
  • FGTI-2734

    CAS:
    FGTI-2734, a dual FT/GGT-1 inhibitor (IC50: 250/520 nM), blocks KRAS membrane binding and curbs KRAS-driven pancreatic cancer.
    Formula:C26H31FN6O2S
    Purity:99.69%
    Color and Shape:Solid
    Molecular weight:510.627
  • Pactimibe sulfate

    CAS:
    Pactimibe sulfate (CS-505) is a dual ACAT1/2 inhibitor for cholesterol metabolism and atherosclerosis research.
    Formula:C50H82N4O10S
    Purity:99.08%
    Color and Shape:Solid
    Molecular weight:931.27
  • Miglustat hydrochloride

    CAS:
    Miglustat hydrochloride (N-Butyldeoxynojirimycin hydrochloride) is an inhibitor of glucosylceramide synthase and can be used for studies about Type I Gaucher
    Formula:C10H22ClNO4
    Purity:99.85%
    Color and Shape:Solid
    Molecular weight:255.74
  • OSMI-1

    CAS:
    OSMI-1: cell-permeable OGT inhibitor, blocks O-GlcNAcylation (IC50: 2.7 μM), no effect on other cell glycans.
    Formula:C28H25N3O6S2
    Purity:96.79% - 99.66%
    Color and Shape:White Solid
    Molecular weight:563.645
  • Darlifarnib

    CAS:
    Darlifarnib (Compound (S)-058) is an inhibitor of farnesyl transferase and geranylgeranyltransferase, with IC50 values of ≤ 10 nM and > 1000 nM, respectively. It exhibits high metabolic stability in human and mouse liver microsomes, with a half-life of over 100 minutes.
    Formula:C29H20N6O
    Color and Shape:Solid
    Molecular weight:468.509
  • Glucosylceramide synthase-IN-4

    CAS:
    Glucosylceramide Synthase-IN-4 (compound 12) serves as a potent inhibitor of glucosylceramide synthase (GCS), exhibiting an IC50 of 6.8 nM. It demonstrates superior pharmacokinetic properties and robust stability in human hepatocytes. Additionally, this compound is noted for its effective CNS penetration and acceptable PXR selectivity [1].
    Formula:C22H18F5N3O3
    Color and Shape:Solid
    Molecular weight:467.39
  • ICMT-IN-55

    CAS:
    ICMT-IN-55 (compound 31) acts as an ICMT inhibitor, exhibiting an IC50 value of 90 nM [1].
    Formula:C22H26F3NO2
    Color and Shape:Solid
    Molecular weight:393.44
  • PF-07202954

    CAS:
    PF-07202954 is a DGAT2 inhibitor with a long half-life. reduce the triglyceride content in the liver of rats fed with a Western diet, NASH.
    Formula:C22H23FN6O3
    Purity:98.99%
    Color and Shape:Yellow Solid
    Molecular weight:438.45