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Ubiquitinación

Ubiquitinación

Los inhibidores de la ubiquitinación son compuestos que interfieren con el proceso de ubiquitinación, mediante el cual las proteínas son marcadas con moléculas de ubiquitina para su degradación por el proteasoma. Estos inhibidores son fundamentales para estudiar el recambio de proteínas, la transducción de señales y la regulación de diversos procesos celulares. La ubiquitinación juega un papel clave en muchas enfermedades, incluyendo el cáncer, los trastornos neurodegenerativos y las disfunciones del sistema inmunológico. Al modular la ubiquitinación, estos inhibidores pueden proporcionar información sobre los mecanismos de la enfermedad y abrir nuevas vías para la intervención terapéutica. En CymitQuimica, ofrecemos una amplia selección de inhibidores de ubiquitinación de alta calidad para apoyar su investigación en biología celular, proteómica y descubrimiento de fármacos.

Subcategorías de "Ubiquitinación"

Se han encontrado 107 productos de "Ubiquitinación"

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  • USP30 inhibitor 18

    CAS:
    <p>USP30 inhibitor 18 is a selective inhibitor of USP30 (IC50 = 0.02 μM). USP30 inhibitor 18 is able to accelerate mitophagy and increase protein ubiquitination.</p>
    Fórmula:C26H28FN3O4S
    Pureza:99.85%
    Forma y color:Solid
    Peso molecular:497.58
  • Cbl-b-IN-13

    CAS:
    <p>Cbl-b-IN-13 (Example 520) is a potent Cbl-b inhibitor exhibiting an IC50 of less than 100 nM and is capable of activating T-cells [1].</p>
    Fórmula:C29H30F3N5O2
    Pureza:98%
    Forma y color:Solid
    Peso molecular:537.58
  • Cbl-b-IN-6

    CAS:
    <p>Cbl-b-IN-6 (Compound 246) is an inhibitor of both casitas B-lineage lymphoma-b (Cbl-b) and c-Cbl, exhibiting inhibitory half-maximal inhibitory concentrations (</p>
    Fórmula:C30H32F5N5O
    Pureza:98%
    Forma y color:Solid
    Peso molecular:573.6
  • Cbl-b-IN-10

    CAS:
    <p>Cbl-b-IN-10 (Compound 463) is a potent inhibitor of both casitas B-lineage lymphoma-b (Cbl-b) and c-Cbl, exhibiting half-maximal inhibitory concentrations (</p>
    Fórmula:C31H37F3N6O
    Pureza:98%
    Forma y color:Solid
    Peso molecular:566.66
  • Cbl-b-IN-9

    CAS:
    <p>Cbl-b-IN-9 (Compound 300) is an inhibitor targeting casitas B-lineage lymphoma-b (Cbl-b) and c-Cbl, exhibiting potent inhibitory activity with half-maximal</p>
    Fórmula:C30H33F3N6O2
    Pureza:98%
    Forma y color:Solid
    Peso molecular:566.62
  • Cbl-b-IN-12

    CAS:
    <p>Cbl-b-IN-12 (Example 10) is an inhibitor of casitas B-lineage lymphoma-b (CBL-B), demonstrating a half-maximal inhibitory concentration (IC50) of less than 100</p>
    Fórmula:C28H29F3N6O2
    Pureza:98%
    Forma y color:Solid
    Peso molecular:538.56
  • Cbl-b-IN-7

    CAS:
    <p>Cbl-b-IN-7 (Compound 248) is an inhibitor of casitas B-lineage lymphoma-b (Cbl-b) and c-Cbl, exhibiting inhibitory half-maximal inhibitory concentrations (IC50s</p>
    Fórmula:C29H31F4N5O2
    Pureza:98%
    Forma y color:Solid
    Peso molecular:557.58
  • Skp2 inhibitor 2

    CAS:
    <p>Skp2 inhibitor 2 (14f) impedes the F-box protein S-phase kinase-associated protein 2 (Skp2), demonstrating an IC50 of 10.2 μM against Skp2-Cks1.</p>
    Fórmula:C27H32N4O
    Pureza:98%
    Forma y color:Solid
    Peso molecular:428.57
  • Cbl-b-IN-8

    CAS:
    <p>Cbl-b-IN-8 (Compound 293) is an inhibitor of both casitas B-lineage lymphoma-b (Cbl-b) and c-Cbl, exhibiting half maximal inhibitory concentrations (IC50s) of 5</p>
    Fórmula:C35H44F3N7O3
    Pureza:98%
    Forma y color:Solid
    Peso molecular:667.76
  • Cbl-b-IN-11

    CAS:
    <p>Cbl-b-IN-11 (Compound 466) is an inhibitor of both casitas B-lineage lymphoma-b (Cbl-b) and c-Cbl, exhibiting half-maximal inhibitory concentrations (IC50s) of</p>
    Fórmula:C31H35F5N6O
    Pureza:98%
    Forma y color:Solid
    Peso molecular:602.64
  • USP7-IN-1

    CAS:
    <p>USP7-IN-1 is a selective and reversible ubiquitin-specific protease 7 (USP7) inhibitor (IC50 = 77 μM).</p>
    Fórmula:C23H24ClN3O3
    Pureza:99.82%
    Forma y color:Solid
    Peso molecular:425.91
  • LDN-91946

    CAS:
    <p>LDN-91946 is an effective and selective inhibitor of ubiquitin C-terminal hydrolase-L1 (UCH-L1) (Ki = 2.8 μM).</p>
    Fórmula:C15H10N2O4S
    Pureza:97.12%
    Forma y color:Solid
    Peso molecular:314.32
  • UPCDC30766

    CAS:
    <p>UPCDC30766, a potent allosteric inhibitor of p97, exhibits an IC50 of 12 nM and is applicable for colon cancer research [1].</p>
    Fórmula:C30H32F2N6O3S
    Pureza:98%
    Forma y color:Solid
    Peso molecular:594.68
  • FT671

    CAS:
    <p>FT671 is a non-covalent and selective inhibitor of USP7 (IC50: 52 nM) It also binds to the USP7 catalytic domain (Kd: 65 nM).</p>
    Fórmula:C24H23F4N7O3
    Pureza:98%
    Forma y color:Solid
    Peso molecular:533.48
  • PYZD-4409

    CAS:
    <p>PYZD-4409 is a selective UBA1 inhibitor with an IC50 of 20 μM.</p>
    Fórmula:C14H7ClFN3O5
    Pureza:99.71%
    Forma y color:Solid
    Peso molecular:351.67
  • CC0651

    CAS:
    <p>CC0651 is a highly selective allosteric inhibitor of human Cdc34 ubiquitin-conjugating enzyme (UCE), inhibiting p27 Kip1 ubiquitination (IC50=1.72 μM).</p>
    Fórmula:C20H21Cl2NO6
    Pureza:99.03%
    Forma y color:Solid
    Peso molecular:442.29
  • UC-764864

    CAS:
    <p>UC-764864, a UBE2N inhibitor, impedes the enzymatic activity of UBE2N and exhibits cytotoxic effects through the disruption of UBE2N-dependent signaling in</p>
    Fórmula:C19H18N2OS
    Pureza:99.3%
    Forma y color:Solid
    Peso molecular:322.42
  • IMP-1710

    CAS:
    <p>IMP-1710 is a selective UCH-L1 inhibitor with an IC50 value of 38 nM in a fluorescence polarization assay.[1]Cost-effective and quality-assured.</p>
    Fórmula:C23H19N5O
    Pureza:99.3%
    Forma y color:Solid
    Peso molecular:381.43
  • BC-1293

    CAS:
    <p>BC-1293 inhibits FBXO24, stabilizes DARS2, and elevates cytokines in mice, showing immunostimulatory potential for immune modulation research.</p>
    Fórmula:C26H28N4O4S
    Pureza:98.40%
    Forma y color:Solid
    Peso molecular:492.59
  • PRC1-IN-1

    CAS:
    <p>PRC1-IN-1 (compound RB-4) is an inhibitor of the polycomb repressive complex 1 (PRC1) with an IC50 of 2.3 μM. It targets RING1B-BMI1, RING1A-BMI1, and RING1B-PCGF1, exhibiting IC50 values of 2.8 μM, 2.6 μM, and 1.8 μM, respectively.</p>
    Fórmula:C24H19ClFN3O2
    Forma y color:Solid
    Peso molecular:435.878