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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 72 products for "Proteasome".

products per page.
  • Bortezomib

    CAS:
    Bortezomib (LDP 341) is a 20S proteasome inhibitor (Ki=0.6 nM) that is reversible and selective.
    Formula:C19H25BN4O4
    Purity:97.79% - >99.99%
    Color and Shape:White Solid
    Molecular weight:384.237
  • Epoxomicin

    CAS:
    Epoxomicin, a selective proteasome inhibitor, chiefly blocks CH-L activity, mildly affecting T-L and PGPH at lower rates.
    Formula:C28H50N4O7
    Purity:98.65% - 98.86%
    Color and Shape:Solid
    Molecular weight:554.7192
  • Carfilzomib

    CAS:
    Carfilzomib (PR-171) is a proteasome inhibitor that irreversibly binds to the chymotrypsin of the 20S proteasome.
    Formula:C40H57N5O7
    Purity:99.6% - 99.92%
    Color and Shape:White Solid
    Molecular weight:719.9099
  • MDL-28170

    CAS:
    MDL-28170 (Calpain Inhibitor III) is a Cysteine protease.
    Formula:C22H26N2O4
    Purity:95.06%
    Color and Shape:Solid
    Molecular weight:382.4528
  • Isoginkgetin

    CAS:
    ISOGINKGETIN (4',4'''-Dimethylamentoflavone), a compound derived from the leaves of Ginkgo biloba, to up-regulate adiponectin secretion.
    Formula:C32H22O10
    Purity:98% - 99.75%
    Color and Shape:Yellow Solid
    Molecular weight:566.5111
  • Oprozomib

    CAS:
    Oprozomib inhibits 20S proteasome β5/LMP7, is orally available, and may have cancer-fighting properties. IC50: β5 - 36 nM; LMP7 - 82 nM.
    Formula:C25H32N4O7S
    Purity:98% - 99.87%
    Color and Shape:White Solid
    Molecular weight:532.609
  • MUN57694

    CAS:
    MUN57694 is an inhibitor of 26S proteasome.
    Formula:C23H25N3O4
    Purity:99%
    Color and Shape:White Solid
    Molecular weight:407.4623
  • Tomatine

    CAS:
    Tomatine (lycopersicin) is an antiproliferatve agent of breast adenocarcinoma cells.
    Formula:C50H83NO21
    Purity:98.42% - 99.93%
    Color and Shape:Solid
    Molecular weight:1034.1881
  • MG-101

    CAS:
    MG-101 (Calpain inhibitor I) is a cell-permeable and potent inhibitor of cysteine proteases including calpains and lysosomal cathepsins.
    Formula:C20H37N3O4
    Purity:97.02% - 98%
    Color and Shape:Solid
    Molecular weight:383.53
  • Bortezomib-pinanediol

    CAS:
    Bortezomib-pinanediol is a proteasome inhibitor. is a prodrug of Bortezomib.
    Formula:C29H39BN4O4
    Purity:97.28%
    Color and Shape:Solid
    Molecular weight:518.455
  • DD1

    CAS:
    DD1 (HUN85111) is a proteasome inhibitor that induces human myeloid tumor-selective apoptosis.
    Formula:C16H14N2O3
    Purity:99.57%
    Color and Shape:Solid
    Molecular weight:282.294
  • Tripterin

    CAS:
    Tripterin (Celastrol) is an proteasome inhibitor for the chymotrypsin-like activity of a purified 20S proteasome with antioxidant and anti-inflammatory effects.
    Formula:C29H38O4
    Purity:98.56% - 99.8%
    Color and Shape:Orange Solid
    Molecular weight:450.61
  • Proteasome inhibitor IX

    CAS:
    Proteasome inhibitor IX (PS-IX) is an inhibitor of chymotrypsin-like activity of the 20S proteasome (IC50 ~1 μM).
    Formula:C20H21B2NO5
    Purity:99.77%
    Color and Shape:Solid
    Molecular weight:377.006
  • Ixazomib

    CAS:
    Ixazomib (MLN2238) is a boron-based peptide proteasome inhibitor targeting β5 site (IC50: 3.4 nM), also affecting β1 and β2 sites.
    Formula:C14H19BCl2N2O4
    Purity:98% - 99.77%
    Color and Shape:Solid
    Molecular weight:361.029
  • Delanzomib

    CAS:
    Delanzomib (CEP-18770) is an oral proteasome inhibitor with an IC50 of 3.8 nM, targeting chymotrypsin-like activity with minimal effect on other activities.
    Formula:C21H28BN3O5
    Purity:95.52% - 99.46%
    Color and Shape:Solid
    Molecular weight:413.275
  • 18α-Glycyrrhetinic acid

    CAS:
    18α-Glycyrrhetinic acid (Enoxolone) is a pentacyclic triterpenoid derivative of the beta-amyrin type obtained from the hydrolysis of glycyrrhizic acid.
    Formula:C30H46O4
    Purity:98.54% - 99.68%
    Color and Shape:Solid
    Molecular weight:470.6838
  • PSI

    CAS:
    PSI is a proteasome inhibitor.
    Formula:C32H50N4O8
    Purity:97% - 98.33%
    Color and Shape:Solid
    Molecular weight:618.76
  • KZR-504

    CAS:
    KZR-504 is a selective inhibitor of immunoproteasome low molecular mass polypeptide 2 (LMP2) (IC50s: 51 nM, 4.274 μM for LMP2 and LMP7, respectively).
    Formula:C21H23N3O6
    Color and Shape:Solid
    Molecular weight:413.4238
  • FK-448 Free base

    CAS:
    FK-448 Free base is an effective and specific inhibitor of chymotrypsin, with an IC50 of 720 nM.
    Formula:C25H30N2O3
    Purity:98%
    Color and Shape:Solid
    Molecular weight:406.52
  • Proteasome-IN-1

    CAS:
    Proteasome-IN-1 is an inhibitor of proteasome.
    Formula:C42H35N5O3
    Purity:98%
    Color and Shape:Solid
    Molecular weight:657.76