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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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  • GSK-114

    CAS:
    GSK-114, a TNNI3K inhibitor with a 25 nM IC50, is 40x more selective than B-Raf and good for in vivo studies.
    Fórmula:C19H23N5O4S
    Pureza:99.51%
    Forma y color:Solid
    Peso molecular:417.48
  • SGX-523

    CAS:
    <p>SGX-523 is a selective Met inhibitor (IC50: 4 nM), no inhibitory to Abl, BRAFV599E, p38α, and c-Raf.</p>
    Fórmula:C18H13N7S
    Pureza:99% - >99.99%
    Forma y color:Solid
    Peso molecular:359.41
  • CID-1067700

    CAS:
    CID-1067700 is one of the first identified competitive inhibitors of nucleotide binding by Ras-related GTPases(Rab7 with a Ki of 13 nM).
    Fórmula:C18H18N2O4S2
    Pureza:99.46%
    Forma y color:Solid
    Peso molecular:390.48
  • 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,
    Fórmula:C8H10NO6P
    Pureza:97.52%
    Forma y color:Solid
    Peso molecular:247.14
  • Cefotetan

    CAS:
    Cefotetan, a cephamycin antibiotic, fights various bacteria by disrupting cell wall synthesis.
    Fórmula:C17H17N7O8S4
    Pureza:95.72% - 99.38%
    Forma y color:Solid
    Peso molecular:575.62
  • PF-06260933

    CAS:
    <p>PF-06260933 is a highly selective small-molecule MAP4K4 inhibitor with IC50s of 3.7 and 160 nM for kinase and cell, respectively.</p>
    Fórmula:C16H13ClN4
    Pureza:99.63% - 99.97%
    Forma y color:Solid
    Peso molecular:296.75
  • Gypenoside L

    CAS:
    Gypenoside L inhibits autophagic flux and induces cell death in human esophageal cancer cells through endoplasm reticulum stress-mediated Ca2+ release.
    Fórmula:C42H72O14
    Pureza:99.42% - 99.65%
    Forma y color:Solid
    Peso molecular:801.01
  • UM-164

    CAS:
    <p>UM-164 (DAS-DFGO-II), a highly potent c-Src inhibitor with a dissociation constant (Kd) of 2.7 nM, also effectively inhibits p38α and p38β.</p>
    Fórmula:C30H31F3N8O3S
    Pureza:98.72% - 99.52%
    Forma y color:Solid
    Peso molecular:640.68
  • NG25 trihydrochloride

    CAS:
    NG25 trihydrochloride: kinase inhibitor for MAP4K2, TAK1, Src, LYN, Abl, CSK, FER, p38α; blocks TNF-α signals; impedes IFN secretion; anti-cancer properties.
    Fórmula:C29H33Cl3F3N5O2
    Forma y color:Solid
    Peso molecular:646.96
  • IACS-13909

    CAS:
    IACS-13909 (BBP-398), a specific and potent allosteric inhibitor of SHP2, that suppresses signaling through the MAPK pathway.
    Fórmula:C17H18Cl2N6
    Pureza:98.8%
    Forma y color:Solid
    Peso molecular:377.27
  • CC-90001

    CAS:
    CC-90001 is an orally administered c-Jun N-terminal kinase (JNK) inhibitor with bias for JNK1 over JNK2.
    Fórmula:C16H27N5O2
    Pureza:99.96%
    Forma y color:Solid
    Peso molecular:321.42
  • Kobe2602

    CAS:
    Kobe 2602 is an inhibitor of Ras that exhibits anticancer chemotherapeutic activities.
    Fórmula:C14H9F4N5O4S
    Pureza:98.36% - 99.39%
    Forma y color:Solid
    Peso molecular:419.31
  • NG25

    CAS:
    NG25 is a potent dual TAK1 and MAP4K2 inhibitor, with IC50s of 149 nM and 21.7 nM, respectively.
    Fórmula:C29H30F3N5O2
    Pureza:98.32% - ≥95%
    Forma y color:Solid
    Peso molecular:537.58
  • 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.
    Fórmula:C20H14ClN3O
    Pureza:≥95%
    Forma y color:Solid
    Peso molecular:347.8
  • Belvarafenib

    CAS:
    Belvarafenib (HM95573) is a potent pan-RAF inhibitor with antitumor activity and inhibits B-RAF, B-RAFv600E, and C-RAF.Cost-effective and quality-assured.
    Fórmula:C23H16ClFN6OS
    Pureza:98% - 99.65%
    Forma y color:Solid
    Peso molecular:478.93
  • AZD8330

    CAS:
    AZD8330 (ARRY-704) is a novel, selective, non-ATP competitive MEK 1/2 inhibitor with IC50 of 7 nM. Phase 1.
    Fórmula:C16H17FIN3O4
    Pureza:98.72%
    Forma y color:Solid
    Peso molecular:461.23
  • methyl 5-(3,4-dimethoxyphenyl)isoxazole-3-carboxylate

    CAS:
    methyl 5-(3,4-dimethoxyphenyl)isoxazole-3-carboxylate is a biochemical.
    Fórmula:C13H13NO5
    Pureza:97.69%
    Forma y color:Solid
    Peso molecular:263.25
  • APS-2-79

    CAS:
    APS-2-79: KSR-dependent MEK inhibitor, blocks ATP biotin at KSR2, IC50 of 120 nM, disrupts Ras-MAPK signaling.
    Fórmula:C23H21N3O3
    Forma y color:Solid
    Peso molecular:387.43
  • Pimasertib HCl

    CAS:
    Pimasertib HCl, an oral MEK1/2 inhibitor, may thwart tumor growth by blocking RAS/RAF/MEK/ERK signaling.
    Fórmula:C15H16ClFIN3O3
    Forma y color:Solid
    Peso molecular:467.66
  • K-Ras(G12C) inhibitor 9

    CAS:
    K-Ras(G12C) inhibitor 9 is an allosteric inhibitor of oncogenic K-Ras(G12C).
    Fórmula:C16H21ClIN3O4S
    Pureza:97.33% - 97.45%
    Forma y color:Solid
    Peso molecular:513.78