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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 893 prodotti di "MAPK"

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  • RAF709

    CAS:
    <p>RAF709 is a novel Raf kinase inhibitor with IC50s of 0.5 and 1.8 nM for c-Raf and b-Raf, respectively.</p>
    Formula:C28H29F3N4O4
    Purezza:99.28% - 99.8%
    Colore e forma:Solid
    Peso molecolare:542.55
  • ASP2453

    CAS:
    ASP2453 is a potent, selective and covalent inhibitor of KRAS G12C.
    Formula:C40H48F3N7O4
    Purezza:99.71%
    Colore e forma:Solid
    Peso molecolare:747.85
  • IACS-13909

    CAS:
    IACS-13909 (BBP-398), a specific and potent allosteric inhibitor of SHP2, that suppresses signaling through the MAPK pathway.
    Formula:C17H18Cl2N6
    Purezza:98.8%
    Colore e forma:Solid
    Peso molecolare:377.27
  • K-Ras(G12C) inhibitor 6

    CAS:
    <p>Irreversible K-Ras(G12C) inhibitor 6 fully modifies the protein at 10 μM after 24h in vitro.</p>
    Formula:C17H22Cl2N2O3S
    Purezza:89.07% - 97.09%
    Colore e forma:Solid
    Peso molecolare:405.34
  • L-779450

    CAS:
    L-779450, an effective, ATP-competitive Raf kinase inhibitor (IC50: 10 nM) , displays >7, >30 and >70-fold selectivity over p38α, GSK3β and Lck respectively.
    Formula:C20H14ClN3O
    Purezza:≥95%
    Colore e forma:Solid
    Peso molecolare:347.8
  • (S)-AMG-510

    CAS:
    (S)-AMG-510 is the S-type compound of AMG-510 (Sotorasib), which effectively and selectively inhibits KRASG12C.Cost-effective and quality-assured.
    Formula:C30H30F2N6O3
    Purezza:99.05% - 99.76%
    Colore e forma:Solid
    Peso molecolare:560.594
  • ASK1-IN-1

    CAS:
    ASK1-IN-1 inhibits apoptosis kinase 1, crucial in cell stress responses, with 21 nM IC50.
    Formula:C19H19N9O2
    Purezza:99.92%
    Colore e forma:Solid
    Peso molecolare:405.41
  • PLX-4720

    CAS:
    PLX-4720 is a potent and selective B-Raf (V600E) inhibitor designed to block the ATP-binding site of oncogenic B-Raf.Cost-effective and quality-assured.
    Formula:C17H14ClF2N3O3S
    Purezza:97.78% - 99.83%
    Colore e forma:Solid
    Peso molecolare:413.83
  • ZT-12-037-01

    CAS:
    Zt-12-037-01 is a ATP competitive STK19 inhibitor(IC50 values of 23.96 nM and 27.94 nM for STK19 (WT) and STK19 (D89N),respectively).
    Formula:C21H31N5O2
    Purezza:99.56%
    Colore e forma:Solid
    Peso molecolare:385.5
  • Cichoric Acid

    CAS:
    Cichoric Acid (Dicaffeoyltartaric acid) is a potent inhibitor of human immunodeficiency virus type-1 (HIV-1) integrase and the replication in tissues.
    Formula:C22H18O12
    Purezza:97.87% - 98.77%
    Colore e forma:Solid
    Peso molecolare:474.37
  • XMD17-109

    CAS:
    <p>XMD17-109 (ERK5-IN-1) is a new selective ERK-5 inhibitor (EC50: 4.2 uM, HEK293 cells).</p>
    Formula:C36H46N8O3
    Purezza:98.75% - 99.7%
    Colore e forma:Solid
    Peso molecolare:638.8
  • Locostatin

    CAS:
    Locostatin is a potent and cell permeable inhibitor of Raf kinase inhibitor protein (RKIP)/Raf1 kinase interaction and an inhibitor of cell migration.
    Formula:C14H15NO3
    Purezza:97.13%
    Colore e forma:Solid
    Peso molecolare:245.27
  • BAY-293

    CAS:
    <p>BAY-293 is a potent, cell-active SOS1 inhibitor that disrupts the KRAS-SOS1 interaction (IC50: 21 nM).</p>
    Formula:C25H28N4O2S
    Purezza:97.16%
    Colore e forma:Solid
    Peso molecolare:448.58
  • ERK-IN-3

    CAS:
    <p>ERK-IN-3 (ASN007 free base) is a potent and orally active inhibitor of ERK.</p>
    Formula:C22H25ClFN7O2
    Purezza:99.55% - 99.76%
    Colore e forma:Solid
    Peso molecolare:473.93
  • BI-78D3

    CAS:
    <p>BI-78D3, a competitive JNK inhibitor. IC50 of BI-78D3 is 280 nM that displays &gt; 100 fold selectivity over p38α, and have no activity at mTOR and PI-3K.</p>
    Formula:C13H9N5O5S2
    Purezza:97.89% - >99.99%
    Colore e forma:Solid
    Peso molecolare:379.37
  • Pyridoxal 5'-phosphate hydrate

    CAS:
    Pyridoxal 5'-phosphate hydrate (PLP)(1:x), the active form of vitamin B6, is a cofactor for many different enzymes involved in transamination reactions,
    Formula:C8H10NO6P
    Purezza:97.52%
    Colore e forma:Solid
    Peso molecolare:247.14
  • sodium lauroyl-α-hydroxyethyl sulfonate

    CAS:
    Sodium houttuyfonate is anti-pseudomonas agents, inhibits virulence-related motility of Pseudomonas.
    Formula:C14H27NaO5S
    Purezza:≥98% - ≥98%
    Colore e forma:Solid
    Peso molecolare:330.41
  • TAO Kinase inhibitor 1

    CAS:
    TAO Kinase inhibitor 1 delays mitosis and induces mitotic cell death.
    Formula:C25H24N2O2
    Purezza:99.74%
    Colore e forma:Solid
    Peso molecolare:384.47
  • CC-401 Hydrochloride

    CAS:
    CC-401 Hydrochloride (CC401 HCl) is a second generation ATP-competitive anthrapyrazolone c-Jun N terminal kinase (JNK) inhibitor with antineoplastic activity.
    Formula:C22H25ClN6O
    Purezza:99.71% - ≥95%
    Colore e forma:Solid
    Peso molecolare:424.93
  • APS-2-79

    CAS:
    APS-2-79: KSR-dependent MEK inhibitor, blocks ATP biotin at KSR2, IC50 of 120 nM, disrupts Ras-MAPK signaling.
    Formula:C23H21N3O3
    Colore e forma:Solid
    Peso molecolare:387.43