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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 893 productos de "MAPK"

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  • EO-1606

    CAS:
    <p>EO-1606 is a p38MAP kinase inhibitor with anti-inflammatory activity and may be used in studies of Alzheimer;s disease and dermatitis.</p>
    Fórmula:C21H17ClFNO
    Pureza:98.28% - 98.84%
    Forma y color:Solid
    Peso molecular:353.82
  • p38α inhibitor 4

    CAS:
    p38α inhibitor 4 is a selective MAPK p38α inhibitor, which is used to study diabetes, pain and chronic inflammation.
    Fórmula:C14H7F6N3O
    Pureza:99.69%
    Forma y color:Solid
    Peso molecular:347.215
  • AKP-001

    CAS:
    AKP-001 is a selective inhibitor of MAPK of the p38α isoform and is used in the study of immune and digestive disorders.
    Fórmula:C21H13ClF2N4O2
    Pureza:99.50% - 99.92%
    Forma y color:Solid
    Peso molecular:426.8
  • p38 MAPK Inhibitor

    CAS:
    <p>p38 MAPK inhibitor is a potent inhibitor of p38 MAP kinase (IC50 = 35 nM). It inhibits senescence induced by the oncogene RAS.</p>
    Fórmula:C20H13ClFN3O
    Pureza:99.91%
    Forma y color:Solid
    Peso molecular:365.79
  • Cot inhibitor-1

    CAS:
    Cot inhibitor-1 selectively blocks Tpl2 kinase, reducing TNF-alpha in blood (IC50: 5.7 nM). It may treat arthritis, IBD, and certain cancers.
    Fórmula:C27H27Cl2FN8
    Pureza:98.87%
    Forma y color:Solid
    Peso molecular:553.46
  • NMDAR/TRPM4-IN-2

    CAS:
    Potent NMDAR/TRPM4-IN-2 blocks NMDAR/TRPM4, protects brain and retinal neurons, and prevents mitochondrial dysfunction with an IC50 of 2.1 μM.
    Fórmula:C11H19BrCl2N2
    Pureza:99.75%
    Forma y color:Solid
    Peso molecular:330.092
  • SOS1-IN-15

    CAS:
    <p>SOS1-IN-15 is an orally active and potent SOS1 inhibitor with potential antitumor activity.SOS1-IN-15 is used in the study of colon cancer.</p>
    Fórmula:C28H27F3N6O2
    Pureza:98.32%
    Forma y color:Solid
    Peso molecular:536.548
  • B-Raf IN 5

    CAS:
    B-Raf IN 5 is a potent inhibitor of the protein kinase B-Raf (IC50: 2.0 nM). B-Raf IN 5 resists rapid metabolism and does not bind to the secondary target PXR.
    Fórmula:C23H18ClF3N6O3S2
    Forma y color:Solid
    Peso molecular:583.01
  • KRAS G12C inhibitor 49

    CAS:
    KRAS G12C inhibitor 49 is an orally active KRAS G12C inhibitor that exhibits antitumour effects.
    Fórmula:C31H31ClN6O3
    Forma y color:Solid
    Peso molecular:571.07
  • SOS1-IN-5

    CAS:
    <p>SOS1-IN-5, a potent pyrimidine inhibitor, disrupts RAS-SOS1, blocking KRAS activation.</p>
    Fórmula:C26H31F3N4O5
    Forma y color:Solid
    Peso molecular:536.54
  • KRAS inhibitor-12

    CAS:
    KRAS inhibitor-12 blocks KRAS G12C (IC50: 0.537 μM) and p-ERK in cancer cells; promising for pancreatic, colorectal, lung cancer study.
    Fórmula:C19H16Cl2FN5OS
    Forma y color:Solid
    Peso molecular:452.33
  • Ras inhibitor 134

    CAS:
    Ras inhibitor 134 can be used in studies about Ras.
    Fórmula:C23H21ClFN5O3
    Forma y color:Soild
    Peso molecular:469.9
  • SOS1-IN-8

    CAS:
    SOS1-IN-8 is an inhibitor of SOS1 and acts on SOS1-G12D (IC50: 11.6 nM) and SOS1-G12V (IC50: 40.7 nM).
    Fórmula:C24H26F3N3O4
    Forma y color:Solid
    Peso molecular:477.48
  • KRAS G12C mutant protein inhibitor A-1

    CAS:
    KRAS G12C mutant protein inhibitor A-1 can be used in studies about Ras.
    Fórmula:C31H26ClF4N7O2
    Forma y color:Solid
    Peso molecular:640.03
  • ERK1/2 inhibitor 7

    CAS:
    ERK1/2 inhibitor 7 is a potent inhibitor of ERK, acting on ERK2 (IC50: 0.94 nM).
    Fórmula:C23H22FN7OS
    Forma y color:Solid
    Peso molecular:463.53
  • GGTI-297

    CAS:
    GGTI-297 is a potent, cell-permeable, and selective peptidomimetic inhibitor of GGTase I compared to Farnesyl Transferase (FTase).
    Fórmula:C26H31N3O3S
    Forma y color:Solid
    Peso molecular:465.61
  • SOS1-IN-14

    CAS:
    SOS1-IN-14 是选择性的、有效的、口服具有活力的 SOS1 抑制剂 (IC50: 3.9 nM)。SOS1-IN-14 能够利用 P-糖蛋白介导的外排机制在肠道内被吸收。SOS1-IN-14 能够用于 KRAS 突变的癌症的研究,且抑瘤效果比 BI-3406 好。
    Fórmula:C29H29F3N6O2
    Forma y color:Solid
    Peso molecular:550.57
  • CMP3a

    CAS:
    CMP3a, a NEK2 inhibitor, hinders GBM in mice and enhances radiotherapy by disrupting EZH2.
    Fórmula:C28H27F3N6O2S
    Forma y color:Solid
    Peso molecular:568.61
  • AMG-548 hydrochloride (864249-60-5 free base)


    AMG-548 hydrochloride is an orally active and selective p38α inhibitor (Ki: 0.5 nM) and shows slightly selective over p38β (Ki: 36 nM) and >1000 fold selective
    Fórmula:C29H28ClN5O
    Pureza:98%
    Forma y color:Solid
    Peso molecular:498.02
  • SOS1-IN-16

    CAS:
    SOS1-IN-16 (Comp 54) serves as a selective SOS1 inhibitor exhibiting an IC50 value of 7.2 nM and demonstrates inhibitory activity against CYP3A4 with an IC50 of
    Fórmula:C30H31F3N4O3
    Pureza:98%
    Forma y color:Solid
    Peso molecular:552.59