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MAPK

MAPK

Le MAPK sono una famiglia di chinasi proteiche coinvolte in una varietà di processi cellulari, tra cui crescita, proliferazione, differenziazione e risposte allo stress. La via di segnalazione MAPK è composta da diversi livelli, tra cui ERK, JNK e p38 MAPK, ciascuno con ruoli distinti nella funzione cellulare. La disregolazione della segnalazione MAPK è collegata al cancro, alle malattie infiammatorie e ai disturbi metabolici. Presso CymitQuimica, offriamo una vasta gamma di inibitori e attivatori delle MAPK per supportare la tua ricerca in biologia cellulare, trasduzione del segnale e meccanismi delle malattie.

Trovati 894 prodotti di "MAPK"

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  • K-Ras G12C-IN-4

    CAS:
    K-Ras G12C-IN-4 是一种 KRAS G12C 共价抑制剂。
    Formula:C31H33ClN4O4
    Purezza:99.00%
    Colore e forma:Solid
    Peso molecolare:561.07
  • Tanzisertib

    CAS:
    Tanzisertib (CC-930) (CC-930) is a potent inhibitor of JNK1/2/3 with IC50s of 61/7/6 nM, respectively, with potential antifibrotic activity.
    Formula:C21H23F3N6O2
    Purezza:98.66% - 99.28%
    Colore e forma:Solid
    Peso molecolare:448.44
  • KRAS G12C inhibitor 19

    CAS:
    KRAS G12C inhibitor 19 is a potent KRAS G12C inhibitor that shows anti-tumor activity in cellular assays, and the family inhibits tumor growth.
    Formula:C25H19ClF2N4O3S
    Purezza:97.46%
    Colore e forma:Solid
    Peso molecolare:528.96
  • GW806742X

    CAS:
    <p>GW806742X inhibits MLKL with Kd 9.3 μM, preventing necroptosis; also targets VEGFR2.</p>
    Formula:C25H22F3N7O4S
    Purezza:98.3%
    Colore e forma:Solid
    Peso molecolare:573.55
  • MAP4K4-IN-3

    CAS:
    MAP4K4-IN-3 (Compound 17) may be a viable target for antidiabetic agents, a serine/threonine protein kinase.
    Formula:C15H12ClN5
    Purezza:98.07%
    Colore e forma:Solid
    Peso molecolare:297.74
  • ACBI3

    CAS:
    <p>ACBI3 is a selective pan-KRAS degrader with anticancer activity that degrades oncogenic KRAS. ACBI3 inhibits the growth of most cancer cell lines driven by KRAS mutations.</p>
    Formula:C50H62N14O6S2
    Purezza:99.24%
    Colore e forma:Solid
    Peso molecolare:1019.25
  • SU3327

    CAS:
    SU3327 (halicin) is a potent, selective and substrate-competitive inhibitor of JNK(IC50 of 0.7 μM).
    Formula:C5H3N5O2S3
    Purezza:98.39%
    Colore e forma:Solid
    Peso molecolare:261.3
  • ARS-1630

    CAS:
    ARS-1630 is a mutant K-ras G12C inhibitor. It is a less active enantiomer of ARS-1620.
    Formula:C21H17ClF2N4O2
    Purezza:97.78%
    Colore e forma:Solid
    Peso molecolare:430.84
  • LUT014

    CAS:
    <p>LUT014 is a B-Raf inhibitor (IC50: 11.7 nM) and developed to decrease dose-limiting acneiform lesions associated with EGFR Inhibitors treatment.</p>
    Formula:C27H19F3N8O
    Purezza:99.03%
    Colore e forma:Solid
    Peso molecolare:528.49
  • MRTX-1257

    CAS:
    MRTX-1257: selective, irreversible KRAS G12C inhibitor; IC50 of 900 pM; 31% bioavailable in mice; 77% target engagement.
    Formula:C33H39N7O2
    Purezza:97.3% - 99.07%
    Colore e forma:Solid
    Peso molecolare:565.71
  • BI-3406

    CAS:
    BI-3406 is an orally active, highly potent and selective between KRAS and Son of Sevenless 1 (SOS1) interaction inhibitor(IC50 : 6 nM),with anticancer activity.
    Formula:C23H25F3N4O3
    Purezza:99.2% - 99.66%
    Colore e forma:Solid
    Peso molecolare:462.46
  • INH154

    CAS:
    INH154 is a potent Nek2 and Hec1 binding (INH) inhibitor with IC50s of 120 nM in MB468 cells and 200 nM in Hela cells for INH.
    Formula:C22H24N4OS
    Purezza:99.95%
    Colore e forma:Solid
    Peso molecolare:392.52
  • PF-3644022

    CAS:
    PF-3644022 is a selective MK2 inhibitor, effective against TNFα (IC50: 5.2 nM, Ki: 3 nM), with anti-inflammatory properties. Also blocks MK3 and PRAK.
    Formula:C21H18N4OS
    Purezza:98.13%
    Colore e forma:Solid
    Peso molecolare:374.46
  • RMC-6236

    CAS:
    <p>RMC-6236 is a potent RAS(ON)MULTI inhibitor with broad-spectrum inhibitory activity against RAS-GTP.Cost-effective and quality-assured.</p>
    Formula:C44H58N8O5S
    Purezza:98.24% - 99.92%
    Colore e forma:Solid
    Peso molecolare:811.05
  • ETC-206

    CAS:
    <p>ETC-206 is a selective inhibitor of MNK1 and MNK2 (IC50s: 64 nM and 86 nM).</p>
    Formula:C25H20N4O2
    Purezza:99.72% - 99.79%
    Colore e forma:Solid
    Peso molecolare:408.45
  • MK2-IN-3 hydrate

    CAS:
    MK2-IN-3 hydrate (MK-2 Inhibitor III) is an orally active, selective, and ATP-competitive inhibitor of MAPKAP-K2 (MK-2) (IC50 of 0.85 nM)
    Formula:C21H18N4O2
    Purezza:99.58%
    Colore e forma:Solid
    Peso molecolare:358.39
  • Divarasib

    CAS:
    <p>Divarasib (GDC-6036), an investigational KRAS G12C inhibitor for solid tumors, has an IC50 of &lt;0.01 μM.</p>
    Formula:C29H32ClF4N7O2
    Purezza:99.237% - 99.83%
    Colore e forma:Solid
    Peso molecolare:622.06
  • CC-90003

    CAS:
    CC-90003 is a selective inhibitor of ERK 1/2. It has antitumor activity.
    Formula:C22H21F3N6O2
    Purezza:99.42%
    Colore e forma:Solid
    Peso molecolare:458.44
  • MRTX0902

    CAS:
    <p>MRTX0902 is an effective and high selective inhibitor of SOS1 with an IC50 of 46 nM and a Ki of 2 nM.</p>
    Formula:C22H24N6O
    Purezza:99.69%
    Colore e forma:Solid
    Peso molecolare:388.47
  • Regorafénib N-oxyde (M2)

    CAS:
    <p>Regorafénib N-oxyde M2 is an active metabolite of Regorafenib.</p>
    Formula:C21H15ClF4N4O4
    Purezza:98.03% - 98.26%
    Colore e forma:Solid
    Peso molecolare:498.81