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Proteasas / Proteasoma

Proteasas / Proteasoma

Los inhibidores de proteasas y proteasomas son compuestos que bloquean la actividad de las proteasas y del proteasoma, que están involucrados en la degradación y renovación de proteínas. Estos inhibidores son vitales para estudiar la regulación de la homeostasis proteica, el control del ciclo celular y la apoptosis. Los inhibidores de proteasas y proteasomas también se utilizan en el tratamiento de enfermedades como el cáncer, donde la degradación anormal de proteínas desempeña un papel en la progresión de la enfermedad. Al inhibir las proteasas o el proteasoma, estos compuestos pueden inducir la muerte celular en células cancerosas y son herramientas esenciales tanto en la investigación básica como en el desarrollo terapéutico. En CymitQuimica, ofrecemos una amplia gama de inhibidores de proteasas y proteasomas de alta calidad para apoyar su investigación en bioquímica, biología celular y desarrollo de fármacos.

Subcategorías de "Proteasas / Proteasoma"

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Se han encontrado 1039 productos de "Proteasas / Proteasoma"

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  • midesteine

    CAS:
    <p>Midesteine (MR-889) is a small molecule neutrophil elastase inhibitor used in the treatment of bronchitis, asthma and chronic lung disease.</p>
    Fórmula:C12H13NO3S3
    Pureza:99.52% - 99.98%
    Forma y color:Solid
    Peso molecular:315.43
  • PF 00356231

    CAS:
    <p>PF 00356231 is a selectivity inhibitor MMP-12 and can be used in studies about the treatment of emphysema and chronic obstructive pulmonary disease (COPD).</p>
    Fórmula:C25H20N2O3S
    Pureza:99.35%
    Forma y color:Solid
    Peso molecular:428.5
  • Histatin 5

    CAS:
    <p>Histatin 5, a human saliva peptide, blocks MMP-2 and MMP-9 at IC50s of 0.57/0.25 μM and kills fungi.</p>
    Fórmula:C133H195N51O33
    Pureza:98%
    Forma y color:Solid
    Peso molecular:3036.29
  • EP 171

    CAS:
    <p>EP 171 is a potent agonist of TP-receptors.</p>
    Fórmula:C23H29FO5
    Forma y color:Solid
    Peso molecular:404.47
  • Sofosbuvir impurity K

    CAS:
    <p>Sofosbuvir impurity K is an diastereoisomer of Sofosbuvir.Sofosbuvir is an HCV RNA replication inhibitor, with potent anti-hepatitis C virus activity.</p>
    Fórmula:C22H29ClN3O9P
    Pureza:98%
    Forma y color:Solid
    Peso molecular:545.91
  • Trivalent hydroxyarsinothricn


    <p>Trivalent hydroxyarsinothricn (R-AST-OH) is a covalent and irreversible inhibitor of kidney-type glutaminase (KGA). It binds to the glutamine binding site and forms a covalent bond with the cysteine residue at the active site. This compound selectively kills triple-negative breast cancer (TNBC) cells without being cytotoxic to control cell lines. KGA is an enzyme that regulates glutamine metabolism and is associated with tumor malignancy.</p>
    Fórmula:C4H10AsNO4
    Peso molecular:210.98258
  • HCV-IN-7 hydrochloride

    CAS:
    HCV-IN-7 hydrochloride: Oral, potent HCV NS5A inhibitor, pan-genotypic, IC50s 3-47 pM, good pharmacokinetics, favorable liver uptake.
    Fórmula:C40H50Cl2N8O6S
    Pureza:98%
    Forma y color:Solid
    Peso molecular:841.85
  • VD2173

    CAS:
    <p>VD2173: a macrocyclic peptide that inhibits HGF serine proteases, matriptase, and hepsin, potentially for lung cancer research.</p>
    Fórmula:C31H45N9O6S
    Forma y color:Solid
    Peso molecular:671.81
  • Procizumab


    <p>Procizumab is a humanized IgG1 antibody that targets dipeptidyl peptidase 3 (DPP3). It shows potential for investigating sepsis. For the isotype control, refer to HumanIgG1kappa, Isotype Control.</p>
    Forma y color:Odour Liquid
  • Sofigatran

    CAS:
    <p>Sofigatran (MCC-977) is an oral anticoagulant targeting thrombin for cardiovascular research.</p>
    Fórmula:C24H44N4O4S
    Forma y color:Solid
    Peso molecular:484.7
  • PSI-353661

    CAS:
    <p>PSI-353661 (GS-558093), inhibits HCV's NS5B polymerase; EC90: 8nM (wild-type), 11nM (S282T); active in human hepatocytes.</p>
    Fórmula:C24H32FN6O8P
    Forma y color:Solid
    Peso molecular:582.52
  • Obtusifolin-2-O-glucoside

    CAS:
    <p>Obtusifolin-2-O-glucoside (compound 7), a tyrosinase inhibitor with an IC50 value of 9.2 μM, can be isolated from cassia seed [1].</p>
    Fórmula:C22H22O10
    Forma y color:Solid
    Peso molecular:446.4
  • Ellipyrone B


    <p>Ellipyrone B, a γ-pyrone-based macrocyclic polyketide with antihyperglycemic properties, demonstrates inhibitory activity against dipeptidyl peptidase-4 (IC 50</p>
    Fórmula:C25H38O7
    Forma y color:Solid
    Peso molecular:450.57
  • NIM811

    CAS:
    <p>NIM811 is an orally bioavailable dual inhibitor of mitochondrial permeability transition and cyclophilin.</p>
    Fórmula:C62H111N11O12
    Pureza:98%
    Forma y color:Solid
    Peso molecular:1202.635
  • Cajaninstilbene acid

    CAS:
    <p>Cajaninstilbene acid is a useful organic compound for research related to life sciences. The catalog number is T124035 and the CAS number is 87402-84-4.</p>
    Fórmula:C21H22O4
    Forma y color:Solid
    Peso molecular:338.403
  • GSK2818713

    CAS:
    <p>GSK2818713 is a novel Hepatitis C NS5A replication complex inhibitor.</p>
    Fórmula:C46H56N8O8
    Forma y color:Solid
    Peso molecular:849.002
  • Tyrosinase-IN-36


    <p>Tyrosinase-IN-36 is a moderately potent inhibitor of tyrosine, exhibiting an inhibition percentage of 42.75% compared to kojic acid at a concentration of 100 μM and possesses antioxidant activity.</p>
    Forma y color:Odour Solid
  • Z-FG-NHO-Bz

    CAS:
    <p>Z-FG-NHO-Bz is a selective inhibitor of cathepsin [1].</p>
    Fórmula:C26H25N3O6
    Forma y color:Solid
    Peso molecular:475.49
  • DPP8/9-IN-1


    <p>DPP8/9-IN-1 (Compound 16) is a selective covalent inhibitor of dipeptidyl peptidase 8 and 9 (DPP8/9), with IC50 values of 14 nM and 298 nM, respectively. It irreversibly binds to the active site serine (such as S730 in DPP9) through a phosphate ester warhead, blocking substrate binding and inhibiting DPP8/9-mediated protein processing. DPP8/9-IN-1 holds potential for research in cancer and inflammatory diseases.</p>
    Forma y color:Odour Solid
  • LMP7/LMP2-IN-1

    CAS:
    <p>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.</p>
    Fórmula:C16H27BN4O3
    Forma y color:Soild
    Peso molecular:334.22