CymitQuimica logo
p38 MAPK

p38 MAPK

p38 MAPKs are a subgroup of MAPKs that respond to stress signals and are involved in the regulation of inflammation, cell differentiation, apoptosis, and autophagy. p38 MAPK signaling is crucial in immune responses and is implicated in various diseases, including chronic inflammatory conditions, cancer, and neurodegenerative disorders. At CymitQuimica, we provide a comprehensive range of p38 MAPK inhibitors and modulators to support your research in inflammation, stress response, and therapeutic development.

Found 117 products of "p38 MAPK"

Sort by

Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
products per page.
  • p38α inhibitor 5

    CAS:
    <p>The compound p38α inhibitor5 (compound 1) is a PROTAC-type ligand that targets p38 and is utilized in the synthesis of NR-11c.</p>
    Formula:C26H23BrF2N2O3
    Color and Shape:Solid
    Molecular weight:529.37
  • Z16078526

    CAS:
    <p>Z16078526 promotes Ucp1, p38 MAPK, lipolysis, thermogenic genes, and mitochondrial activity in mouse brown adipocytes.</p>
    Formula:C18H17N3O4S
    Purity:98.93%
    Color and Shape:Solid
    Molecular weight:371.41
  • p38α inhibitor 3

    CAS:
    <p>p38α inhibitor 3 is a inhibitor of the mitogen-activated protein kinase p38α that can block the effectiveness of myoblast differentiation.</p>
    Formula:C19H20FNO
    Purity:99.94%
    Color and Shape:Soild
    Molecular weight:297.37
  • p38 MAP Kinase Inhibitor Ⅵ

    CAS:
    <p>p38 MAP Kinase Inhibitor Ⅵ is a potent p38 MAP Kinase inhibitor with anti-inflammatory activity.</p>
    Formula:C16H13FN2OS2
    Purity:98.53%
    Color and Shape:Solid
    Molecular weight:332.42
  • PDE4-IN-26


    <p>PDE4-IN-26 (Compound A5) is an orally active, highly selective inhibitor of PDE4. It exhibits anti-inflammatory properties by inhibiting p38 MAPK phosphorylation. In mouse models of acute lung injury and chronic obstructive pulmonary disease, PDE4-IN-26 reduces lung inflammation, damage, and fibrosis, while promoting sputum secretion and alleviating cough. It is useful for researching lung injury-related diseases.</p>
    Formula:C22H18F2N4O3S
    Color and Shape:Solid
    Molecular weight:456.47
  • WYE-687

    CAS:
    <p>WYE-687 is a selective mTOR inhibitor (IC50: 7 nM), over 100x more selective for mTOR than PI3Kα/γ, affecting mTORC1/pS6K and mTORC2/P-AKT(S473).</p>
    Formula:C28H32N8O3
    Purity:99.93%
    Color and Shape:Solid
    Molecular weight:528.61
  • R1487 Hydrochloride

    CAS:
    <p>R1487 Hydrochloride (R1487 (Hydrochloride)) is an orally bioavailable and highly selective inhibitors of p38α.</p>
    Formula:C19H19ClF2N4O3
    Purity:99.42%
    Color and Shape:Solid
    Molecular weight:424.83
  • Adezmapimod

    CAS:
    <p>Adezmapimod (SB 203580) is a p38 MAPK inhibitor (IC50=0.3-0.5 μM) that is selective and ATP-competitive.</p>
    Formula:C21H16FN3OS
    Purity:99.42% - 99.93%
    Color and Shape:White Solid
    Molecular weight:377.43
  • Talmapimod

    CAS:
    <p>Talmapimod (SCIO-469): Oral ATP-competitive p38α inhibitor, IC50 = 9 nM (p38α), 90 nM (p38β), &gt;2000-fold selectivity over 20 kinases.</p>
    Formula:C27H30ClFN4O3
    Purity:98% - 99.9%
    Color and Shape:Solid
    Molecular weight:513
  • SB 202190

    CAS:
    <p>SB 202190 (FHPI) is a p38 MAPK inhibitor that inhibits p38α and p38β2 (IC50=50/100 nM) selectively and cell-permeably.</p>
    Formula:C20H14FN3O
    Purity:98% - 99.84%
    Color and Shape:Pale Yellow
    Molecular weight:331.34
  • BMS582949

    CAS:
    <p>BMS-582949 inhibits p38 MAPK with 13 nM IC50, blocking kinase activity and activation.</p>
    Formula:C22H26N6O2
    Purity:98.11%
    Color and Shape:Solid
    Molecular weight:406.48
  • Andrograpanin

    CAS:
    <p>Andrograpanin (19-HYDROXY-8(17),13-LABDADIEN-16,15-OLIDE) is a bioactive compound from Andrographis paniculata.</p>
    Formula:C20H30O3
    Purity:99.03% - 99.457%
    Color and Shape:Solid
    Molecular weight:318.45
  • 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
    Purity:98.72% - 99.52%
    Color and Shape:Solid
    Molecular weight:640.68
  • ASK1-IN-1

    CAS:
    <p>ASK1-IN-1 inhibits apoptosis kinase 1, crucial in cell stress responses, with 21 nM IC50.</p>
    Formula:C19H19N9O2
    Purity:99.92%
    Color and Shape:Solid
    Molecular weight:405.41
  • Cornuside

    CAS:
    <p>Cornuside boosts immunity, reduces inflammation, protects heart and liver, and guards against brain injury by modulating stress responses.</p>
    Formula:C24H30O14
    Purity:99.86% - >99.99%
    Color and Shape:Solid
    Molecular weight:542.49
  • Rotundic acid

    CAS:
    <p>Rotundic acid fights various cancers: HepG2, A375, NCI-H446, MCF-7, and HT-29.</p>
    Formula:C30H48O5
    Purity:96.91% - 99.97%
    Color and Shape:Solid
    Molecular weight:488.7
  • FERULIC ACID METHYL ESTER

    CAS:
    <p>FERULIC ACID METHYL ESTER (Methyl ferulate) is a hydroxycinnamic acid that is abundant in plants. FERULIC ACID METHYL ESTER has antioxidant activities.</p>
    Formula:C11H12O4
    Purity:99.66% - 99.95%
    Color and Shape:Solid
    Molecular weight:208.21
  • Gypenoside L

    CAS:
    <p>Gypenoside L inhibits autophagic flux and induces cell death in human esophageal cancer cells through endoplasm reticulum stress-mediated Ca2+ release.</p>
    Formula:C42H72O14
    Purity:99.42% - 99.65%
    Color and Shape:Solid
    Molecular weight:801.01
  • Pexmetinib

    CAS:
    <p>Pexmetinib (ARRY-614) is an orally bioavailable dual p38 MAPK/Tie-2 inhibitor.Cost-effective and quality-assured.</p>
    Formula:C31H33FN6O3
    Purity:99.07% - 99.66%
    Color and Shape:Solid
    Molecular weight:556.63
  • SB 239063

    CAS:
    <p>SB 239063 (SB239063) is a potent and selective p38 MAPKα/β inhibitor with IC50 of 44 nM, showing no activity against the γ- and δ-kinase isoforms.</p>
    Formula:C20H21FN4O2
    Purity:99.42% - 99.81%
    Color and Shape:Solid
    Molecular weight:368.4