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MAPK

MAPK

Las MAPK son una familia de quinasas de proteínas involucradas en una variedad de procesos celulares, incluyendo crecimiento, proliferación, diferenciación y respuestas al estrés. La vía de señalización MAPK consta de varios niveles, incluidos ERK, JNK y p38 MAPK, cada uno con roles distintos en la función celular. La desregulación de la señalización MAPK está vinculada al cáncer, las enfermedades inflamatorias y los trastornos metabólicos. En CymitQuimica, ofrecemos una amplia gama de inhibidores y activadores de MAPK para apoyar su investigación en biología celular, transducción de señales y mecanismos de enfermedades.

Se han encontrado 894 productos de "MAPK"

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  • SCH 51344

    CAS:
    SCH 51344 inhibits Ras induced malignant transformation. SCH 51344 prevents anchorage-independent growth of oncogene transformed fibroblasts [1].
    Fórmula:C16H20N4O3
    Forma y color:Solid
    Peso molecular:316.36
  • BAY-846

    CAS:
    BAY-846: allosteric MEK inhibitor, long-lasting, highly bioavailable, low brain entry, effective in K-Ras A549 model.
    Fórmula:C19H13F4IN4O4S
    Forma y color:Solid
    Peso molecular:596.29
  • 3,4-Dephostatin

    CAS:
    3,4-Dephostatin is an inhibitor of the interactions of CFTR-associated ligand (CAL) and PSD-95/Dlg1/ZO-1 (PDZ) domain.
    Fórmula:C7H8N2O3
    Forma y color:Solid
    Peso molecular:168.15
  • LX-3

    CAS:
    LX-3 activates p38 MAPK, enabling expression of genes normally silenced by DNA methylation.
    Fórmula:C20H13BrN4OS
    Forma y color:Solid
    Peso molecular:437.31
  • Spiclomazine HCl

    CAS:
    Spiclomazine HCl induced apoptosis in pancreatic cancer cells, which was generally related to cell viability, migration, and invasion.
    Fórmula:C22H25Cl2N3OS2
    Forma y color:Solid
    Peso molecular:482.49
  • KRAS G12C inhibitor 47

    CAS:
    KRAS G12C inhibitor 47 strongly blocks KRAS G12C (IC50: 0.172 μM) and p-ERK in cells; promising for pancreatic, colorectal, lung cancers.
    Fórmula:C30H28ClFN4O3
    Forma y color:Solid
    Peso molecular:547.02
  • SOS1-IN-3

    CAS:
    SOS1-IN-3 is an effective inhibitor of SOS1 (son of sevenless homolog 1) (IC50=5 nM). SOS1-IN-3 shows antitumor activity.
    Fórmula:C21H21F3N4O
    Forma y color:Solid
    Peso molecular:402.41
  • SOS1 activator 1

    CAS:
    SOS1 activator 1 enhances SOS1's GDP-GTP exchange on Ras (Kd: 44 nM).
    Fórmula:C26H32ClFN6
    Forma y color:Solid
    Peso molecular:483.02
  • PF-04880594

    CAS:
    PF-04880594 is a potent and selective RAF inhibitor which inhibits both wild-type and mutant BRAF and CRAF. PF-04880594 exhibits antitumor activity [1].
    Fórmula:C19H16F2N8
    Forma y color:Solid
    Peso molecular:394.38
  • Ras modulator-1

    CAS:
    Ras modulator-1 is a modulator of Ras.
    Fórmula:C29H21N5O4S
    Forma y color:Solid
    Peso molecular:535.57
  • KRAS G12C inhibitor 48


    KRAS G12C inhibitor 48: potent with IC50 639.91 nM; hampers H358, H23, A549 cell growth with IC50s of 0.796, 6.33, 16.14 µM, respectively.
    Fórmula:C36H39ClN8O2
    Forma y color:Solid
    Peso molecular:651.2
  • Cuspin-1

    CAS:
    Cuspin-1, a small molecule, increases SMN levels by 50% in SMA by boosting ERK phosphorylation and Ras-Raf-MEK signaling.
    Fórmula:C13H10BrNO
    Forma y color:Solid
    Peso molecular:276.13
  • RMM-46

    CAS:
    <p>RMM-46 is a reversible covalent inhibitor with high ligand efficiency and selectivity for MSK/RSK family kinases.</p>
    Fórmula:C24H26N4O5
    Pureza:98.89%
    Forma y color:Solid
    Peso molecular:450.49
  • B-Raf IN 7

    CAS:
    "B-Raf IN 7 inhibits B-Raf (IC50: 110.23 nM); fights colon, breast, liver, cervical, prostate cancers (IC50: 7.50-12.83 μM)."
    Fórmula:C15H16N6O3
    Forma y color:Solid
    Peso molecular:328.33
  • KRAS G12C inhibitor 31

    CAS:
    KRAS G12C inhibitor 31 is an inhibitor of KRAS G12C that can be used to study cancer.
    Fórmula:C25H22ClFN6O3
    Forma y color:Solid
    Peso molecular:508.93
  • 6-T-GDP

    CAS:
    6-T-GDP (6-Thioguanosine 5'-diphosphate) is a metabolite of thiopurine. It inhibits the activity of Rac1, thereby reducing the transcription of inflammatory factors and the expression of cell adhesion molecules, which ultimately suppresses leukocyte migration and the occurrence of tissue inflammation.
    Fórmula:C10H15N5O10P2S
    Forma y color:Solid
    Peso molecular:459.27
  • GDC-0879

    CAS:
    GDC-0879 (AR-00341677) is a novel, potent and selective B-Raf inhibitor with IC50 of 0.13 nM with activity against c-Raf as well.
    Fórmula:C19H18N4O2
    Pureza:99.62%
    Forma y color:Solid
    Peso molecular:334.37
  • mSIRK

    CAS:
    mSIRK (G-Protein βγ Binding Peptide) is an ERK1 and ERK2 dual activator that promotes alpha-subunit dissociation.
    Fórmula:C93H150N20O25
    Pureza:99.26%
    Forma y color:Solid
    Peso molecular:1948.31
  • Tpl2-IN-I

    CAS:
    Tpl2-IN-I is an inhibitor of tumour progression locus 2 (Tpl2) kinase.
    Fórmula:C21H14ClFN6
    Pureza:98%
    Forma y color:Solid
    Peso molecular:404.83
  • NSC1011

    CAS:
    NSC1011 is an inhibitor of ras converting enzyme 1 (Rce1).
    Fórmula:C23H18N2O3
    Pureza:98%
    Forma y color:Solid
    Peso molecular:370.4