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Cisteina proteasi

Cisteina proteasi

Gli inibitori delle proteasi a cisteina sono composti che mirano e inibiscono le proteasi a cisteina, una classe di enzimi che degradano le proteine rompendo i legami peptidici in cui un residuo di cisteina agisce come nucleofilo. Questi enzimi sono coinvolti in vari processi fisiologici, tra cui l'apoptosi, la risposta immunitaria e il turnover proteico. Gli inibitori delle proteasi a cisteina sono cruciali per lo studio di malattie come il cancro, i disturbi neurodegenerativi e le infezioni parassitarie. Presso CymitQuimica, offriamo inibitori delle proteasi a cisteina per supportare la tua ricerca in proteolisi, regolazione cellulare e scoperta di farmaci.

Trovati 110 prodotti di "Cisteina proteasi"

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  • CatD-IN-1

    CAS:
    CatD-IN-1 (Compound 5) is a Cathepsin D inhibitor with an IC50 of 0.44 μM, and it shows potential for research in the field of osteoarthritis.
    Formula:C18H18Cl2N4O5
    Colore e forma:Solid
    Peso molecolare:441.265
  • GB111-NH2

    CAS:
    GB111-NH2, a cysteine cathepsin inhibitor, is applicable in cancer research [1].
    Formula:C33H39N3O6
    Colore e forma:Solid
    Peso molecolare:573.68
  • Verducatib

    CAS:
    <p>Verducatib is an inhibitor of cathepsins (cathepsin).</p>
    Formula:C31H35FN4O3
    Colore e forma:Solid
    Peso molecolare:530.633
  • Z-FY-CHO

    CAS:
    Pyridoxal (Pyridoxaldehyde), a component of vitamin B6, is an aldehyde obtained by oxidizing pyridoxine and is widely found in plants and animals.
    Formula:C26H26N2O5
    Purezza:95.88%
    Colore e forma:Solid
    Peso molecolare:446.5
  • Cathepsin C-IN-5

    CAS:
    <p>Cathepsin C-IN-5 (SF38) is a potent, oral Cathepsin C blocker with an IC50 of 59.9 nM; less active against Cat L/S/B/K; has anti-inflammatory effects.</p>
    Formula:C21H17ClN6OS
    Colore e forma:Solid
    Peso molecolare:436.92
  • Dual Cathepsin L/JAK-IN-1

    CAS:
    DualCathepsinL/JAK-IN-1 (Compound A8) serves as a dual inhibitor of Cathepsin L (CTSL) and JAK, exhibiting IC50 values of 0.68 μM for CTSL and 337.1 nM, 5.251 nM, 27.29 nM, and 172.6 nM for JAK1/2/3 and TYK2, respectively. This compound effectively prevents the activation of MAPK, NF-κB, and JAK/STAT signaling pathways, leading to significant anti-inflammatory therapeutic effects. DualCathepsinL/JAK-IN-1 is applicable in research on acute lung injury (ALI).
    Formula:C19H18ClN5
    Colore e forma:Solid
    Peso molecolare:351.833
  • Z-Val-Val-Nle-diazomethylketone

    CAS:
    Z-Val-Val-Nle-diazomethylketone is an inhibitor of cathepsin S (CATS). It significantly suppresses the upregulation of IFNg-induced MHCII molecules, specifically HLA-DR and Ii-p33/35, while increasing the protein level of Ii-p10. This compound can be utilized for research into skin disorders such as psoriasis, atopic dermatitis, and actinic keratosis.
    Formula:C25H37N5O5
    Colore e forma:Solid
    Peso molecolare:487.59
  • MIV-247

    CAS:
    MIV-247 is a cathepsin S inhibitor that attenuates mechanically abnormal pain in preclinical neuropathic pain models and can be used to study myocardial injury.
    Formula:C17H24F3N3O4
    Purezza:99.27%
    Colore e forma:Solid
    Peso molecolare:391.39
  • PD 151746

    CAS:
    PD151746: calpain inhibitor, Ki μ-calpain=0.26μM, Ki m-calpain=5.33μM; reduces oxLDL cytotoxicity.
    Formula:C11H8FNO2S
    Purezza:98.63% - ≥95%
    Colore e forma:Solid
    Peso molecolare:237.25
  • ALLM

    CAS:
    ALLM (Calpain inhibitor II), a potent calpain and cathepsin protease inhibitor, not only prevents neuronal cell death but also enhances chronic neurological function following spinal cord injury (SCI)[1][2].
    Formula:C19H35N3O4S
    Purezza:98%
    Colore e forma:White Powder
    Peso molecolare:401.56

    Ref: TM-T14187

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