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MAPK

MAPK

MAPKs are a family of protein kinases involved in a variety of cellular processes, including growth, proliferation, differentiation, and stress responses. The MAPK signaling pathway consists of several tiers, including ERK, JNK, and p38 MAPKs, each playing distinct roles in cellular function. Dysregulation of MAPK signaling is linked to cancer, inflammatory diseases, and metabolic disorders. At CymitQuimica, we offer a wide array of MAPK inhibitors and activators to support your research in cell biology, signal transduction, and disease mechanisms.

Found 901 products for "MAPK". Showing the first 500.

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  • TINK-IN-1

    CAS:
    TINK-IN-1 is a selective and potent TNIK inhibitor (IC50: 8 nM).TINK-IN-1 inhibits colorectal cancer cell viability and can be used to study mental retardation.
    Formula:C24H24N4O3
    Purity:99.8%
    Color and Shape:Solid
    Molecular weight:416.47

    Ref: TM-T77660

    1mg
    39.00€
    2mg
    50.00€
    5mg
    82.00€
    10mg
    120.00€
    25mg
    236.00€
    50mg
    353.00€
    100mg
    517.00€
    500mg
    1,099.00€
  • HI-TOPK-032

    CAS:
    HI-TOPK-032 is an effective and specific inhibitor of TOPK.
    Formula:C20H11N5OS
    Purity:98.52%
    Color and Shape:Solid
    Molecular weight:369.4

    Ref: TM-T15481

    2mg
    44.00€
    5mg
    65.00€
    1mL*10mM (DMSO)
    71.00€
    10mg
    87.00€
    25mg
    178.00€
    50mg
    304.00€
    100mg
    522.00€
  • MRTX0902

    CAS:
    MRTX0902 is an effective and high selective inhibitor of SOS1 with an IC50 of 46 nM and a Ki of 2 nM.
    Formula:C22H24N6O
    Purity:99.69%
    Color and Shape:Solid
    Molecular weight:388.47

    Ref: TM-T9755

    1mg
    90.00€
    5mg
    192.00€
    10mg
    281.00€
    25mg
    597.00€
    50mg
    954.00€
    100mg
    1,558.00€
  • BAS 00489700

    CAS:
    BAS 00489700 is a N-UTR interaction inhibitor. BAS 00489700 inhibits virus replication in cell culture.
    Formula:C19H16N2O4
    Purity:99.78%
    Color and Shape:Solid
    Molecular weight:336.34

    Ref: TM-T67854

    1mg
    85.00€
    5mg
    170.00€
    1mL*10mM (DMSO)
    170.00€
    10mg
    250.00€
    25mg
    371.00€
    50mg
    522.00€
    100mg
    712.00€
    200mg
    954.00€
  • Ro-3201195

    CAS:

    Ro-3201195 is a novel orally available p38 MAPK inhibitor with high selectivity.

    Formula:C19H18FN3O4
    Purity:99.15%
    Color and Shape:Solid
    Molecular weight:371.36

    Ref: TM-T68134

    1mg
    128.00€
    5mg
    304.00€
    10mg
    457.00€
    25mg
    747.00€
    50mg
    1,026.00€
    100mg
    1,406.00€
    500mg
    2,812.00€
  • MK2-IN-3 hydrate

    CAS:
    MK2-IN-3 hydrate (MK-2 Inhibitor III) is an orally active, selective, and ATP-competitive inhibitor of MAPKAP-K2 (MK-2) (IC50 of 0.85 nM)
    Formula:C21H18N4O2
    Purity:99.58%
    Color and Shape:Solid
    Molecular weight:358.39

    Ref: TM-T12058

    1mg
    34.00€
    5mg
    60.00€
    1mL*10mM (DMSO)
    73.00€
    10mg
    87.00€
    25mg
    172.00€
    50mg
    250.00€
    100mg
    350.00€
    200mg
    480.00€
  • SU3327

    CAS:
    SU3327 (halicin) is a potent, selective and substrate-competitive inhibitor of JNK(IC50 of 0.7 μM).
    Formula:C5H3N5O2S3
    Purity:98.39%
    Color and Shape:Solid
    Molecular weight:261.3

    Ref: TM-T13018

    2mg
    35.00€
    5mg
    62.00€
    10mg
    90.00€
    1mL*10mM (DMSO)
    93.00€
    25mg
    170.00€
    50mg
    295.00€
    100mg
    447.00€
  • JNK-IN-13

    CAS:
    JNK-IN-13 is a JNK inhibitor that inhibits JNK3 and JNK2 and can be used in the study of diabetes, inflammation, and neurological disorders.
    Formula:C13H7ClN4S
    Purity:98.74%
    Color and Shape:Solid
    Molecular weight:286.74

    Ref: TM-T77694

    10mg
    37.00€
    25mg
    54.00€
    50mg
    88.00€
  • BAY 2965501

    CAS:
    BAY 2965501 is a potent and selective diacylglycerol kinase zeta (DGKζ) inhibitor that induces pERK activation.BAY 2965501 can be used in the study of cancer.
    Formula:C20H19FN4O3S
    Purity:99.89%
    Color and Shape:Solid
    Molecular weight:414.45

    Ref: TM-T73053

    1mg
    87.00€
    5mg
    178.00€
    10mg
    334.00€
    25mg
    620.00€
    50mg
    802.00€
    100mg
    1,108.00€
  • CC-90003

    CAS:
    CC-90003 is a selective inhibitor of ERK 1/2. It has antitumor activity.
    Formula:C22H21F3N6O2
    Purity:99.42%
    Color and Shape:Solid
    Molecular weight:458.44

    Ref: TM-T14894

    1mg
    46.00€
    5mg
    84.00€
    1mL*10mM (DMSO)
    85.00€
    10mg
    130.00€
    25mg
    250.00€
    50mg
    356.00€
    100mg
    532.00€
  • Divarasib

    CAS:
    Divarasib (GDC-6036), an investigational KRAS G12C inhibitor for solid tumors, has an IC50 of <0.01 μM.
    Formula:C29H32ClF4N7O2
    Purity:99.23% - 99.83%
    Color and Shape:Solid
    Molecular weight:622.06

    Ref: TM-T9972

    1mg
    220.00€
    5mg
    522.00€
    1mL*10mM (DMSO)
    707.00€
    10mg
    737.00€
    25mg
    1,161.00€
    50mg
    1,603.00€
    100mg
    2,133.00€
  • KRAS G12C inhibitor 19

    CAS:
    KRAS G12C inhibitor 19 is a potent KRAS G12C inhibitor that shows anti-tumor activity in cellular assays, and the family inhibits tumor growth.
    Formula:C25H19ClF2N4O3S
    Purity:97.46%
    Color and Shape:Solid
    Molecular weight:528.96

    Ref: TM-T40286

    1mg
    86.00€
    5mg
    177.00€
    10mg
    265.00€
    25mg
    515.00€
    50mg
    737.00€
    100mg
    1,018.00€
  • LUT014

    CAS:
    LUT014 is a B-Raf inhibitor (IC50: 11.7 nM) and developed to decrease dose-limiting acneiform lesions associated with EGFR Inhibitors treatment.
    Formula:C27H19F3N8O
    Purity:99.03%
    Color and Shape:Solid
    Molecular weight:528.49

    Ref: TM-T15794

    1mg
    40.00€
    5mg
    90.00€
    1mL*10mM (DMSO)
    94.00€
    10mg
    111.00€
    25mg
    197.00€
    50mg
    278.00€
    100mg
    388.00€
  • Kinase Inhibitor Library


    A unique collection of 2720 kinase inhibitors/regulators for high throughput screening and high content screening for drug discovery in kinase related diseases;
    Color and Shape:Odour Solid

    Ref: TM-L1600

    1mg
    To inquire
    10μL*10mM (DMSO)
    To inquire
    20μL*10mM (DMSO)
    To inquire
    30μL*10mM (DMSO)
    To inquire
    50μL*10mM (DMSO)
    To inquire
    100μL*10mM (DMSO)
    To inquire
    250μL*10mM (DMSO)
    To inquire
  • ERK1/2 inhibitor 10


    ERK1/2 inhibitor 10 (Compound 36c) is a potent inhibitor of ERK1 and ERK2, with IC50 values of 0.11 nM and 0.08 nM, respectively. It effectively hinders the phosphorylation of downstream substrates p90RSK and c-Myc. Additionally, ERK1/2 inhibitor 10 induces apoptosis and incomplete autophagy-related cell death. This compound demonstrates significant antitumor efficacy in models of triple-negative breast cancer and colorectal cancer harboring BRAF and RAS mutations.
    Formula:C23H20ClN5O2S
    Molecular weight:465.10262

    Ref: TM-T209644

    10mg
    To inquire
    50mg
    To inquire
  • MAPK Inhibitor Library


    A unique collection of 365 compounds targeting MAPK signaling for drug discovery in MAPK related diseases;
    Color and Shape:Odour Solid

    Ref: TM-L1400

    1mg
    To inquire
    10μL*10mM (DMSO)
    To inquire
    20μL*10mM (DMSO)
    To inquire
    30μL*10mM (DMSO)
    To inquire
    50μL*10mM (DMSO)
    To inquire
    100μL*10mM (DMSO)
    To inquire
    250μL*10mM (DMSO)
    To inquire
  • PROTAC ERK5 degrader-1

    CAS:
    PROTACERK5 degrader-1 (compound 2) is a bifunctional ERK5 PROTAC degrader. It induces the degradation of ERK5 in MOLT-4 cells via a VHL-mediated proteasome pathway. PROTACERK5 degrader-1 is useful for studying diseases or disorders characterized by abnormal ERK5 activity.
    Formula:C54H67F3N10O6S
    Color and Shape:Solid
    Molecular weight:1041.23

    Ref: TM-T210807

    10mg
    To inquire
    50mg
    To inquire
  • ASP6918


    ASP6918 is a potent, orally active KRAS G12C inhibitor with an IC50 of 0.028 µM. It inhibits cell growth and demonstrates antitumor activity.
    Formula:C36H43N7O3
    Molecular weight:621.34274

    Ref: TM-T209141

    10mg
    To inquire
    50mg
    To inquire
  • KRASG12C IN-14


    KRASG12C IN-14 (compound 15), a potent inhibitor specifically designed for the KRAS G12C mutation, exhibits impressive efficacy in impeding CYPA-dependent KRAS-BRAF interaction and ERK phosphorylation in NCI-H358 cells, both with an IC 50 of 0.002 μM.
    Formula:C51H65F4N9O9S2
    Color and Shape:Solid
    Molecular weight:1088.24

    Ref: TM-T200204

    10mg
    To inquire
    50mg
    To inquire
  • Antimicrobial agent-21

    CAS:
    Antimicrobial agent-21 is a potent mitogen activated protein kinase inhibitor with antibacterial, anti-inflammatory and antitumor activity for the treatment of
    Formula:C18H13N3OS
    Purity:99.82%
    Color and Shape:Solid
    Molecular weight:319.38

    Ref: TM-T67942

    1mg
    54.00€
    5mg
    116.00€
    10mg
    172.00€
    1mL*10mM (DMSO)
    180.00€
    25mg
    278.00€
    50mg
    371.00€
    100mg
    510.00€
    200mg
    687.00€