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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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  • RBC6

    CAS:
    RBC6 is an inhibitor of the binding of Ral to its effector RALBP1.
    Formula:C16H14Cl2N4O2
    Purezza:98%
    Colore e forma:Solid
    Peso molecolare:365.21
  • CP-944629

    CAS:
    CP-944629 is a novel, potent, and selective inhibitor of p38alpha.
    Formula:C19H15F3N4O
    Purezza:98%
    Colore e forma:Solid
    Peso molecolare:372.34
  • BNC-1

    CAS:
    BNC-1 reduces amyloid in mice, enhances synapses by activating Elk-1.
    Formula:C16H14N2O3
    Purezza:98%
    Colore e forma:Solid
    Peso molecolare:282.29
  • ERK1/2 inhibitor 1

    CAS:
    <p>ERK1/2 inhibitor 1 is a potent, orally bioavailable ERK1/2 inhibitor, showing 60% inhibition at 1 nM and an IC50 of 3.0 nM against ERK1 and ERK2, respectively.</p>
    Formula:C29H32ClN5O4
    Purezza:98.81%
    Colore e forma:Solid
    Peso molecolare:550.05
  • PF-05381941

    CAS:
    PF-05381941 is a selective and potent dual inhibitor of TAK1 and p38α that inhibits the kinase activity of TAK1 by binding to its active site.
    Formula:C27H26N6O2
    Purezza:98.04%
    Colore e forma:Solid
    Peso molecolare:466.53
  • MEK-IN-1

    CAS:
    MEK-IN-1 is a MEK inhibitor.
    Formula:C24H20N4O4
    Purezza:98%
    Colore e forma:Solid
    Peso molecolare:428.44
  • PAF (C16)

    CAS:
    <p>PAF (C16) is a potent MAPK and MEK/ERK activator that induces increased vascular permeability.</p>
    Formula:C26H54NO7P
    Purezza:98%
    Colore e forma:Solid
    Peso molecolare:523.68
  • B-Raf IN 13

    CAS:
    <p>B-Raf IN 13 is a potent B-Raf inhibitor with anticancer activity.B-Raf IN 13 has an IC50 of 3.55 nM in the BRAF V600E enzyme assay.</p>
    Formula:C19H19ClFN3O4S
    Purezza:99.41% - >99.99%
    Colore e forma:Soild
    Peso molecolare:439.89
  • KRAS G12D inhibitor 10

    CAS:
    KRAS G12D inhibitor 10 targets KRAS G12D in cancer research (WO2021108683A1, compound 34).
    Formula:C33H41ClN8O2
    Colore e forma:Solid
    Peso molecolare:617.18
  • GGTI-286

    CAS:
    GGTI-286: GGTase I inhibitor, cell-permeable, IC50=2μM. Strongly blocks Rap1A geranylation; less effective on H-Ras, Ras4B IC50=1μM.
    Formula:C23H31N3O3S
    Colore e forma:Solid
    Peso molecolare:429.58
  • LY-2584702 hydrochloride

    CAS:
    <p>Ly-2584702 hydrochloride is a p70S6K selective ATP competitive inhibitor with IC50 of 4 nM.In the S6K1 enzyme assay, the IC50 of LY-2584702 was 2 nM.</p>
    Formula:C21H20ClF4N7
    Purezza:98%
    Colore e forma:Solid
    Peso molecolare:481.88
  • MCP110

    CAS:
    MCP110 is an inhibitor of the interaction of Ras with Raf-1 and can be used in studies about the treatment of human tumors.
    Formula:C33H36N2O3
    Purezza:97.23%
    Colore e forma:Oil
    Peso molecolare:508.65
  • KYA1797

    CAS:
    KYA1797 inhibits Wnt/ß-catenin, targeting axin, and promotes ß-catenin/Ras decay, halting APC/KRAS mutant CRC growth.
    Formula:C17H12N2O6S2
    Purezza:98%
    Colore e forma:Solid
    Peso molecolare:404.42
  • RSK2-IN-2

    CAS:
    RSK2-IN-2 (Compound 25) is a reversible covalent inhibitor of the RPS6KA3 ( RSK2 ) kinase which also inhibits MSK1, MSK2, and RSK3 [1].
    Formula:C16H11N5O
    Colore e forma:Solid
    Peso molecolare:289.29
  • GABAB receptor antagonist 1

    CAS:
    (E)-GABAB receptor antagonist 1 decreases GABA-induced IP3 (inositol trisphosphate) production with IC50 of 37.9 μM.GABAB receptor antagonist 1 is a selective
    Formula:C18H24O4
    Purezza:98%
    Colore e forma:Solid
    Peso molecolare:304.38
  • B-Raf IN 8

    CAS:
    B-Raf IN 8: strong B-Raf inhibitor (70.65 nM IC50); combats liver, colon, breast & prostate cancer with IC50s from 9.78 to 29.85 μM.
    Formula:C18H17N3O2
    Colore e forma:Solid
    Peso molecolare:307.35
  • (2Z,3Z)-U0126

    CAS:
    U0126 selectively inhibits MEK1/2, blocks MAPK/ERK signaling, and suppresses Ki-ras-induced cell growth, with IC50s of 72 nM and 58 nM for MEK1/2.
    Formula:C18H16N6S2
    Colore e forma:Solid
    Peso molecolare:380.49
  • HPK1-IN-24

    CAS:
    HPK1-IN-24 (example 51) has potential to be used in the cancer research which is an inhibitor of hematopoietic progenitor kinase 1 (HPK1) (Ki = 100 nM) [1].
    Formula:C19H14FN5
    Colore e forma:Solid
    Peso molecolare:331.35
  • Migoprotafib

    CAS:
    Migoprotafib (GDC-1971) is a potent and highly selective SHP2 (Src Homology-2 Domain-Containing Phosphatase 2) inhibitor for advanced solid tumours.
    Formula:C25H26N8O
    Purezza:98.31%
    Colore e forma:Solid
    Peso molecolare:454.53
  • UC-857993

    CAS:
    UC-857993 is a selective SOS1-Ras inhibitor with a Kd of 14.7 μM that inhibits ERK, Ras, and reduces MEF growth.
    Formula:C25H22ClNO2
    Colore e forma:Solid
    Peso molecolare:403.9