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Proteasome

Proteasome

Proteasome inhibitors are compounds that inhibit the proteasome, a large protein complex responsible for degrading unwanted or damaged proteins within the cell. Inhibition of the proteasome leads to the accumulation of proteins, which can induce cell cycle arrest and apoptosis, particularly in rapidly dividing cells like cancer cells. Proteasome inhibitors are crucial in cancer research and therapy, especially in the treatment of multiple myeloma and other hematologic malignancies. At CymitQuimica, we offer proteasome inhibitors to support your research in oncology, cell biology, and drug development.

Found 94 products of "Proteasome"

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  • Alloxan monohydrate

    CAS:
    <p>Alloxan Monohydrate is a glucose analog used to induce diabetes by destroying beta-cells.</p>
    Formula:C4H4N2O5
    Purity:99.01% - 99.42%
    Color and Shape:Off-White To Beige-Yellowish Crystalline Powder
    Molecular weight:160.09
  • ARV-471

    CAS:
    <p>ARV-471 (Vepdegestrant) is a orally active Cereblon -based estrogen receptor (ER) PROTAC degrader. ARV-471 is developed for the research of breast cancer.</p>
    Formula:C45H49N5O4
    Purity:97.15% - >99.99%
    Color and Shape:Solid
    Molecular weight:723.9
  • Omarigliptin

    CAS:
    <p>Omarigliptin is a potent and selective oral dipeptidyl peptidase 4 (DPP4) inhibitor with IC50 value of 1.6 nM. Cost-effective and quality-assured.</p>
    Formula:C17H20F2N4O3S
    Purity:99.68% - 99.77%
    Color and Shape:Solid
    Molecular weight:398.43
  • Calpeptin

    CAS:
    <p>Calpeptin is a potent, cell-permeable calpain inhibitor.</p>
    Formula:C20H30N2O4
    Purity:97.06% - 98.33%
    Color and Shape:White To Off-White Powder
    Molecular weight:362.46
  • Talabostat mesylate

    CAS:
    <p>Talabostat mesylate (PT100): Oral DPP4 inhibitor, IC50 0.18 nM, targets tumor-linked proteins, boosts hematopoiesis.</p>
    Formula:C10H23BN2O6S
    Purity:98% - 99.91%
    Color and Shape:Solid
    Molecular weight:310.18
  • PI-1840

    CAS:
    <p>PI-1840 is a reversible and selective chymotrypsin-like (CT-L) inhibitor, with little proteasome proteolytic effects on trypsin-like (T-L) and PGPH-L.</p>
    Formula:C22H26N4O3
    Purity:98.82%
    Color and Shape:Solid
    Molecular weight:394.47
  • 4'-Hydroxychalcone

    CAS:
    <p>4'-Hydroxychalcone (2-Benzal-4-Hydroxyacetophenone) is a chalcone metabolite with hepatoprotective activity</p>
    Formula:C15H12O2
    Purity:99.86% - 99.87%
    Color and Shape:Yellow-Cream Powder
    Molecular weight:224.25
  • ONX-0914

    CAS:
    <p>ONX-0914 (PR-957) is an effective and specific immunoproteasome inhibitor, which has minimal cross-reactivity for the constitutive proteasome.</p>
    Formula:C31H40N4O7
    Purity:98.24% - 99.31%
    Color and Shape:Solid
    Molecular weight:580.67
  • Bortezomib

    CAS:
    <p>Bortezomib (LDP 341) is a 20S proteasome inhibitor (Ki=0.6 nM) that is reversible and selective.</p>
    Formula:C19H25BN4O4
    Purity:97.79% - >99.99%
    Color and Shape:Yellow Solid
    Molecular weight:384.24
  • Epoxomicin

    CAS:
    <p>Epoxomicin, a selective proteasome inhibitor, chiefly blocks CH-L activity, mildly affecting T-L and PGPH at lower rates.</p>
    Formula:C28H50N4O7
    Purity:98.65% - 98.86%
    Color and Shape:White To Off-White Solid
    Molecular weight:554.72
  • Carfilzomib

    CAS:
    <p>Carfilzomib (PR-171) is a proteasome inhibitor that irreversibly binds to the chymotrypsin of the 20S proteasome.</p>
    Formula:C40H57N5O7
    Purity:99.6% - 99.84%
    Color and Shape:Solid
    Molecular weight:719.91
  • MDL-28170

    CAS:
    <p>MDL-28170 (Calpain Inhibitor III) is a Cysteine protease.</p>
    Formula:C22H26N2O4
    Purity:95.06%
    Color and Shape:Solid
    Molecular weight:382.45
  • ISOGINKGETIN

    CAS:
    <p>ISOGINKGETIN (4',4'''-Dimethylamentoflavone), a compound derived from the leaves of Ginkgo biloba, to up-regulate adiponectin secretion.</p>
    Formula:C32H22O10
    Purity:98% - 99.72%
    Color and Shape:Solid
    Molecular weight:566.51
  • Oprozomib

    CAS:
    <p>Oprozomib inhibits 20S proteasome β5/LMP7, is orally available, and may have cancer-fighting properties. IC50: β5 - 36 nM; LMP7 - 82 nM.</p>
    Formula:C25H32N4O7S
    Purity:98% - 99.87%
    Color and Shape:Solid
    Molecular weight:532.61
  • UAMC00039 dihydrochloride

    CAS:
    <p>UAMC00039 dihydrochloride is a potent, reversible and competitive dipeptidyl peptidase II inhibitor with an IC50 of 0.48 nM.</p>
    Formula:C16H26Cl3N3O
    Purity:>99.99%
    Color and Shape:Solid
    Molecular weight:382.76
  • MUN57694

    CAS:
    <p>MUN57694 is an inhibitor of 26S proteasome.</p>
    Formula:C23H25N3O4
    Purity:99%
    Color and Shape:Solid
    Molecular weight:407.46
  • Saxagliptin

    CAS:
    <p>Saxagliptin (BMS-477118) is a selective and reversible DPP4 inhibitor with IC50 of 26 nM.</p>
    Formula:C18H25N3O2
    Purity:99.17% - 99.95%
    Color and Shape:Solid
    Molecular weight:315.41
  • Tomatine

    CAS:
    <p>Tomatine (lycopersicin) is an antiproliferatve agent of breast adenocarcinoma cells.</p>
    Formula:C50H83NO21
    Purity:98.42% - 99.94%
    Color and Shape:White To Light Yellow
    Molecular weight:1034.19
  • MG-101

    CAS:
    <p>MG-101 (Calpain inhibitor I) is a cell-permeable and potent inhibitor of cysteine proteases including calpains and lysosomal cathepsins.</p>
    Formula:C20H37N3O4
    Purity:98% - ≥98%
    Color and Shape:Solid
    Molecular weight:383.53
  • Bortezomib-pinanediol

    CAS:
    <p>Bortezomib-pinanediol is a proteasome inhibitor. is a prodrug of Bortezomib.</p>
    Formula:C29H39BN4O4
    Purity:97.5%
    Color and Shape:Yellow Solid
    Molecular weight:518.46