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Proteassoma

Proteassoma

Os inibidores de proteassoma são compostos que inibem o proteassoma, um grande complexo proteico responsável pela degradação de proteínas indesejadas ou danificadas dentro da célula. A inibição do proteassoma leva ao acúmulo de proteínas, o que pode induzir a parada do ciclo celular e a apoptose, especialmente em células de rápida divisão, como as células cancerosas. Os inibidores de proteassoma são cruciais na pesquisa e terapia do câncer, especialmente no tratamento do mieloma múltiplo e outras malignidades hematológicas. Na CymitQuimica, oferecemos inibidores de proteassoma para apoiar sua pesquisa em oncologia, biologia celular e desenvolvimento de fármacos.

Foram encontrados 72 produtos para "Proteassoma".

produtos por página.
  • Z-LLF-CHO

    CAS:
    Z-LLF-CHO (Z-Leu-Leu-Phe-CHO) effectively inhibits the chymotrypsin-like activity of the pituitary multicatalytic proteinase complex with a Ki value of 460 nM.
    Fórmula:C29H39N3O5
    Pureza:98%
    Cor e Forma:Solid
    Peso molecular:509.64
  • BC-23

    CAS:
    BC-23 (NSC 45382) is a proteasome inhibitor with antitumor and antimicrobial activity for the study of leukemia and small cell lung cancer.
    Fórmula:C21H14ClN3O4S
    Pureza:99.99%
    Cor e Forma:Solid
    Peso molecular:439.87
  • 20S Proteasome activator 1

    CAS:
    20S Proteasome activator 1: IC50—0.3 μM (trypsin), 0.7 μM (chymotrypsin), 1.8 μM (caspase); reduces alpha-synuclein A53T, aids neurodegenerative studies.
    Fórmula:C27H19ClF2N2OS
    Pureza:99.82%
    Cor e Forma:Solid
    Peso molecular:492.97
  • Arimoclomol

    CAS:
    Arimoclomol (BRX-220 free base) is a co-inducer of heat shock proteins (HSP) and can be used in studies about the treatment of amyotrophic lateral sclerosis (
    Fórmula:C14H20ClN3O3
    Pureza:99.15%
    Cor e Forma:Solid
    Peso molecular:313.78
  • LONP1-IN-2

    CAS:
    LONP1-IN-2 is a selective LONP1 inhibitor (IC50=0.187 μM, >10 μM vs 20S) for cancer research.
    Fórmula:C16H27BN4O4
    Pureza:99.61%
    Cor e Forma:Solid
    Peso molecular:350.22
  • Proteasome-IN-5

    CAS:
    Proteasome-IN-5, also known as compound 5, acts as a proteasome inhibitor [1].
    Fórmula:C20H30BN5O7
    Pureza:98%
    Cor e Forma:Solid
    Peso molecular:463.29
  • Proteasome β2c/i-IN-1

    CAS:
    Proteasome β2c/i-IN-1 (compound 37) serves as a selective inhibitor targeting the β2c and β2i subunits of the human proteasome [1].
    Fórmula:C32H48N4O7
    Pureza:98%
    Cor e Forma:Solid
    Peso molecular:600.75
  • LU-002i

    CAS:
    LU-002i is a selective inhibitor targeting the human proteasome subunits β2c and β2i, demonstrating an inhibitory concentration (IC50) of 220 nM for β2i [1].
    Fórmula:C35H52N4O7
    Pureza:98%
    Cor e Forma:Solid
    Peso molecular:640.81
  • ZINC09518833

    CAS:
    ZINC09518833 is an α-ketoamide non-peptide proteasome inhibitor with an IC50 value of 12.4 μM. It can bind with both the active and inactive sites of the proteasome. ZINC09518833 shows promise for use in research related to multiple myeloma (MM).
    Fórmula:C24H25N3O5
    Cor e Forma:Solid
    Peso molecular:435.4724
  • TCL1

    CAS:
    TCL1 acts as a selective non-covalent inhibitor targeting the Pru domain of the Rpn-13 subunit within the 19S regulatory particle (19S RP) of the proteasome, with an IC50 value around 26 μM. It disrupts the recognition and transport of ubiquitinated proteins by Rpn-13, thus inhibiting proteasomal degradation and affecting intracellular protein metabolism balance. TCL1 holds potential for research in hematologic malignancies.
    Fórmula:C19H14BrClN4O2S
    Cor e Forma:Solid
    Peso molecular:477.762
  • LMP7/LMP2-IN-1

    CAS:
    LMP7/LMP2-IN-1 (Compound 19) is an orally effective inhibitor targeting the immunoproteasome subunits LMP7 and LMP2, with respective IC50 values of 257 and 10 nM. This compound reduces the production of antibodies and downregulates the B cells in the germinal centers of the spleen and plasma cells in NP-OVA immunized mice. It has potential applications in the study of autoimmune diseases.
    Fórmula:C16H27BN4O3
    Cor e Forma:Soild
    Peso molecular:334.22
  • Immunoproteasome activator 1

    CAS:
    Immunoproteasome Activator 1 (compound A) is a selective immunoproteasome activator that enhances the presentation of individual MHC-I binding peptides by over 100 times. It binds to the proteasomal structural subunit PSMA1 and facilitates the association of the proteasome activators PA28α/β (PSME1/PSME2) with the immunoproteasome.
    Fórmula:C24H23N3O3
    Cor e Forma:Solid
    Peso molecular:401.4577