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Ubiquitination

Ubiquitination

Ubiquitination inhibitors are compounds that interfere with the process of ubiquitination, where proteins are tagged with ubiquitin molecules for degradation by the proteasome. These inhibitors are critical for studying protein turnover, signal transduction, and the regulation of various cellular processes. Ubiquitination plays a key role in many diseases, including cancer, neurodegenerative disorders, and immune system dysfunction. By modulating ubiquitination, these inhibitors can provide insights into the mechanisms of disease and open up new avenues for therapeutic intervention. At CymitQuimica, we offer a wide selection of high-quality ubiquitination inhibitors to support your research in cell biology, proteomics, and drug discovery.

Subcategories of "Ubiquitination"

Found 107 products of "Ubiquitination"

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  • C527

    CAS:
    C527 is a is a pan DUB enzyme inhibitor. Which has a high potency for the USP1/UAF1 complex (IC50=0.88 μM).
    Formula:C17H8FNO3
    Purity:97.22%
    Color and Shape:Solid
    Molecular weight:293.25
  • WS-383

    CAS:
    WS-383 is a selective, potent and reversible DCN1-UBC12 interaction inhibitor(IC50 of 11 nM).
    Formula:C18H21Cl2N9S2
    Purity:98.46%
    Color and Shape:Solid
    Molecular weight:498.46
  • IU1-47

    CAS:
    IU1-47 是一种特异性 USP14抑制剂,IC50为 0.6 μM。它诱导培养的神经元中 tau 蛋白降解。它抑制 IsoT/USP5, IC50为 20 μM。
    Formula:C19H23ClN2O
    Purity:98.94%
    Color and Shape:Solid
    Molecular weight:330.85
  • NSC232003

    CAS:
    NSC232003 is a highly potent and cell-permeable inhibitor of UHRF1.
    Formula:C6H7N3O3
    Purity:97.72%
    Color and Shape:Solid
    Molecular weight:169.14
  • ML-792

    CAS:
    ML-792 is a specific small ubiquitin-like modifier activating enzyme (SUMO) inhibitor.Cost-effective and quality-assured.
    Formula:C21H23BrN6O5S
    Purity:99.32% - 99.82%
    Color and Shape:Solid
    Molecular weight:551.41
  • TAS4464 hydrochloride

    CAS:
    TAS4464 hydrochloride is a highly potent and selective NEDD8 activating enzyme (NAE) inhibitor(IC50 of 0.955 nM).
    Formula:C21H24ClFN6O6S
    Purity:98.61% - 98.96%
    Color and Shape:Solid
    Molecular weight:542.97
  • MF-094

    CAS:
    MF-094 is a selective USP30 inhibitor with IC50 of 0.12 μM. MF-094 can increase protein ubiquitination and accelerate mitophagy.Cost-effective and quality-assured.
    Formula:C30H37N3O4S
    Purity:99.93%
    Color and Shape:Solid
    Molecular weight:535.7
  • HBX 19818

    CAS:
    <p>HBX 19818 is a specific ubiquitin-specific protease 7 (USP7) inhibitor (IC50: 28.1 μM).</p>
    Formula:C25H28ClN3O
    Purity:97.71%
    Color and Shape:Solid
    Molecular weight:421.96
  • USP8-IN-2

    CAS:
    <p>USP8-IN-2 is a potent inhibitor of the deubiquitinating enzymes USP7 and USP8, with an IC50 of 4.0 μM against USP8D.</p>
    Formula:C19H20ClF3N4OS
    Purity:99.92%
    Color and Shape:Solid
    Molecular weight:444.9
  • Skp2 inhibitor 3


    Skp2 inhibitor 3 (E35), a potent antitumor agent, acts as a robust inhibitor of S-phase kinase-associated protein 2 (SKP2) with an IC50 of 4.86 μM for Skp2-Cks1 binding. It significantly suppresses colony formation and migration, while inducing cell cycle arrest in the S-phase.
    Color and Shape:Odour Solid
  • OTUB2-IN-1


    OTUB2-IN-1 is an OTUB2 inhibitor with antitumor activity and can be used to study skin cancer and non-small cell lung cancer (NSCLC).
    Formula:C19H18N2O6S2
    Purity:98.19%
    Color and Shape:Solid
    Molecular weight:434.49
  • Cbl-b-IN-15


    Cbl-b-IN-15 (compound 25) is an inhibitor of the RING finger E3 ubiquitin ligase Cbl, demonstrating an IC50 of 15 nM. Cbl-b refers to Casitas B-lineage Lymphoma proto-oncogene-b, which can inhibit the activation of T cells, natural killer (NK) cells, and B cells. Cbl-b-IN-15 can activate T cell function with an EC50 of 0.41 μM.
    Formula:C27H27N5O3
    Molecular weight:469.21139
  • Post-Translational Modification Compound Library


    <p>Contains xnum active small molecules for research related to post-translational modifications (PTMs);</p>
    Color and Shape:Odour Solid
  • USP8-IN-3

    CAS:
    <p>USP8-IN-3 is a potent inhibitor of the deubiquitinating enzymes USP7 and USP8, with IC50 of 4.0 μM against USP8D.</p>
    Formula:C18H18F3N5O2S
    Purity:99.79%
    Color and Shape:Solid
    Molecular weight:425.43
  • Rugonersen sodium

    CAS:
    Rugonersen sodium is a locked nucleic acid (LNA)-modified antisense oligonucleotide (ASO) designed to reduce the silencing of ubiquitin protein ligase E3A (UBE3A). Angelman syndrome (AS) refers to a severe neurodevelopmental disorder caused by the loss of neuronal E3 ligase UBE3A, and Rugonersen has been studied for its potential use in the treatment of AS.
    Formula:C204H235N63Na19O109P19S19
    Molecular weight:6948.00
  • dCeMM3 

    CAS:
    <p>dCeMM3 is a glue degrader that induces ubiquitination and degradation of cyclin K by promoting CDK12-cyclin K interaction with CRL4B ligase.</p>
    Formula:C14H11ClN4OS
    Purity:98.48% - 99.41%
    Color and Shape:Solid
    Molecular weight:318.78
  • Ubiquitination Compound Library


    A unique collection of xnum ubiquitination related small chemicals can be used for high throughput and high content screening;
    Color and Shape:Odour Solid
  • SAE-IN-2


    SAE-IN-2 (compound 6) is a potent inhibitor of sumoylation-activating enzyme (SAE) with an IC50 value of 27.8 nM.
    Formula:C27H30ClN5O5S2
    Molecular weight:603.13769
  • OTUB1/USP8-IN-1 HCl


    <p>OTUB1/USP8-IN-1 HCL is a potent dual inhibitor of OTUB1 and USP8 with potential antitumour activity, inhibiting both OTUB1 and USP8 for leukaemia</p>
    Formula:C22H17Cl2FN2O4
    Purity:99.92%
    Color and Shape:Solid
    Molecular weight:463.29
  • RNF5 agonist 1

    CAS:
    RNF5 agonist 1 (analog-1), a structural analog of the RNF5 inhibitor inh-02, is a potent RNF5 agonist. In CFBE41o- cells expressing F508del-CFTR, RNF5 agonist 1 enhances the ubiquitination of ATG4B.
    Formula:C22H18N4S
    Color and Shape:Solid
    Molecular weight:370.47