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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 892 prodotti di "MAPK"

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  • 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,
    Formula:C8H10NO6P
    Purezza:97.52%
    Colore e forma:Solid
    Peso molecolare:247.14
  • 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).
    Formula:C18H18N2O4S2
    Purezza:99.46%
    Colore e forma:Solid
    Peso molecolare:390.48
  • 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.
    Formula:C19H23N5O4S
    Purezza:99.51%
    Colore e forma:Solid
    Peso molecolare:417.48
  • 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>
    Formula:C16H13ClN4
    Purezza:99.63% - 99.97%
    Colore e forma:Solid
    Peso molecolare: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.
    Formula:C42H72O14
    Purezza:99.42% - 99.65%
    Colore e forma:Solid
    Peso molecolare: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>
    Formula:C30H31F3N8O3S
    Purezza:98.72% - 99.52%
    Colore e forma:Solid
    Peso molecolare: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.
    Formula:C29H33Cl3F3N5O2
    Colore e forma:Solid
    Peso molecolare:646.96
  • CC-90001

    CAS:
    CC-90001 is an orally administered c-Jun N-terminal kinase (JNK) inhibitor with bias for JNK1 over JNK2.
    Formula:C16H27N5O2
    Purezza:99.96%
    Colore e forma:Solid
    Peso molecolare:321.42
  • Kobe2602

    CAS:
    Kobe 2602 is an inhibitor of Ras that exhibits anticancer chemotherapeutic activities.
    Formula:C14H9F4N5O4S
    Purezza:98.36% - 99.39%
    Colore e forma:Solid
    Peso molecolare:419.31
  • NG25

    CAS:
    NG25 is a potent dual TAK1 and MAP4K2 inhibitor, with IC50s of 149 nM and 21.7 nM, respectively.
    Formula:C29H30F3N5O2
    Purezza:98.32% - ≥95%
    Colore e forma:Solid
    Peso molecolare:537.58
  • IACS-13909

    CAS:
    IACS-13909 (BBP-398), a specific and potent allosteric inhibitor of SHP2, that suppresses signaling through the MAPK pathway.
    Formula:C17H18Cl2N6
    Purezza:98.8%
    Colore e forma:Solid
    Peso molecolare:377.27
  • 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.
    Formula:C23H16ClFN6OS
    Purezza:98% - 99.65%
    Colore e forma:Solid
    Peso molecolare: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.
    Formula:C16H17FIN3O4
    Purezza:98.72%
    Colore e forma:Solid
    Peso molecolare:461.23
  • methyl 5-(3,4-dimethoxyphenyl)isoxazole-3-carboxylate

    CAS:
    methyl 5-(3,4-dimethoxyphenyl)isoxazole-3-carboxylate is a biochemical.
    Formula:C13H13NO5
    Purezza:97.69%
    Colore e forma:Solid
    Peso molecolare: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.
    Formula:C23H21N3O3
    Colore e forma:Solid
    Peso molecolare:387.43
  • Refametinib

    CAS:
    Refametinib (RDEA119) (RDEA119, Bay 86-9766) is an effective, ATP non-competitive and specific inhibitor of MEK1/2 (IC50: 19/47 nM).
    Formula:C19H20F3IN2O5S
    Purezza:99.85% - >99.99%
    Colore e forma:Solid
    Peso molecolare:572.34
  • K-Ras(G12C) inhibitor 9

    CAS:
    K-Ras(G12C) inhibitor 9 is an allosteric inhibitor of oncogenic K-Ras(G12C).
    Formula:C16H21ClIN3O4S
    Purezza:97.33% - 97.45%
    Colore e forma:Solid
    Peso molecolare:513.78
  • Cichoric Acid

    CAS:
    Cichoric Acid (Dicaffeoyltartaric acid) is a potent inhibitor of human immunodeficiency virus type-1 (HIV-1) integrase and the replication in tissues.
    Formula:C22H18O12
    Purezza:97.87% - 98.77%
    Colore e forma:Solid
    Peso molecolare:474.37
  • K-Ras(G12C) inhibitor 6

    CAS:
    <p>Irreversible K-Ras(G12C) inhibitor 6 fully modifies the protein at 10 μM after 24h in vitro.</p>
    Formula:C17H22Cl2N2O3S
    Purezza:89.07% - 97.09%
    Colore e forma:Solid
    Peso molecolare:405.34
  • GS87

    CAS:
    GS87 is a highly specific inhibitor of GSK3 (glycogen synthase kinase 3) that induces extensive differentiation of AML cells.
    Formula:C16H11N5O2S
    Purezza:98.86%
    Colore e forma:Solid
    Peso molecolare:337.36