
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 887 products of "MAPK"
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p38α inhibitor 2
CAS:<p>P38α Inhibitor 2, a potent and selective inhibitor of p38α MAPK, exhibits a pIC50 value of 9.6.</p>Formula:C27H33N5O3Color and Shape:SolidMolecular weight:475.58pan-KRAS-IN-16
CAS:<p>3344 is an inhibitor of KRAS-effector interactions,with an affnity of 126nm.</p>Formula:C24H26N2O3Purity:98%Color and Shape:SolidMolecular weight:390.47B-Raf IN 6
CAS:<p>B-Raf IN 6: potent B-Raf kinase inhibitor, IC50 of 1.7 nM, doesn't target PXR, metabolically stable, potential in cancer research.</p>Formula:C24H21F3N6O2S2Color and Shape:SolidMolecular weight:546.59(R)-CE3F4
CAS:<p>(R)-CE3F4 is a selective inhibitor of exchange protein directly activated by cAMP isoform 1 (Epac1)(IC50 of 4.2 μM),</p>Formula:C11H10Br2FNOColor and Shape:SolidMolecular weight:351.01SR-3737
CAS:<p>SR-3737 is potent both JNK3 and p38 inhibitor.</p>Formula:C29H25FN4O4Purity:98%Color and Shape:SolidMolecular weight:512.53TOPK-p38/JNK-IN-1
CAS:<p>TOPK-p38/JNK-IN-1 (Compound B12) is an orally active inhibitor of the TOPK-p38/JNK signaling pathway, with an IC50 value of 2.14 μM for the inhibition of NO</p>Formula:C17H15F3N2O4Color and Shape:SolidMolecular weight:368.31B-Raf IN 7
CAS:<p>"B-Raf IN 7 inhibits B-Raf (IC50: 110.23 nM); fights colon, breast, liver, cervical, prostate cancers (IC50: 7.50-12.83 μM)."</p>Formula:C15H16N6O3Color and Shape:SolidMolecular weight:328.33KB-5246
CAS:<p>KB-5246, displays antibacterial activities.is a tetracyclic quinolone.</p>Formula:C18H17ClFN3O4SPurity:98%Color and Shape:SolidMolecular weight:425.86KRas G12C inhibitor 4
CAS:KRas G12C inhibitor 4 is a compound that inhibits KRas G12C.Formula:C33H38ClN7O2Purity:98%Color and Shape:SolidMolecular weight:600.15Avutometinib potassium
CAS:<p>Avutometinib potassium, a MEKi, blocks Delta and Omicron infection in airway cells, potentially lessening disease severity.</p>Formula:C21H17FKN5O5SColor and Shape:SolidMolecular weight:509.553,4-Dephostatin
CAS:<p>3,4-Dephostatin is an inhibitor of the interactions of CFTR-associated ligand (CAL) and PSD-95/Dlg1/ZO-1 (PDZ) domain.</p>Formula:C7H8N2O3Color and Shape:SolidMolecular weight:168.15ERK5-IN-3
CAS:<p>ERK5-IN-3 inhibits ERK5 strongly (IC50: 6 nM) and hampers Hela cell growth (IC50: 31 nM).</p>Formula:C24H23Cl2FN4O2Color and Shape:SolidMolecular weight:489.37Ras modulator-1
CAS:<p>Ras modulator-1 is a modulator of Ras.</p>Formula:C29H21N5O4SColor and Shape:SolidMolecular weight:535.57KRas G12C inhibitor 3
CAS:<p>KRas G12C inhibitor 3 is a compound that inhibits KRas G12C.</p>Formula:C32H36ClN7O2Purity:98%Color and Shape:SolidMolecular weight:586.13MW108
CAS:<p>MW108 is an active site targeted, CNS-active, p38αMAPK inhibitor.</p>Formula:C21H19ClN4Color and Shape:SolidMolecular weight:362.86(S)-CCG-1423
<p>(S)-CCG-1423, a stereoisomer, inhibits Rho to block myocardin-related transcription factor A & serum response signaling.</p>Formula:C18H13ClF6N2O3Purity:98%Color and Shape:SolidMolecular weight:454.8K-Ras G12C-IN-3
CAS:<p>K-Ras G12C-IN-3: novel, irreversible inhibitor of K-Ras G12C mutant protein for cancer treatment.</p>Formula:C21H19Cl3N2O3Color and Shape:SolidMolecular weight:453.75ML 3403
CAS:<p>p38 MAPK inhibitor; IC50: 0.38μM. Reduces IL-1β & TNF-α release in PBMC assay; IC50: 0.039μM & 0.16μM.</p>Formula:C23H21FN4SColor and Shape:SolidMolecular weight:404.5CCG-232601
CAS:<p>CCG-232601 is a inhibitor of the Rho/MRTF/SRF transcriptional pathway.</p>Formula:C24H20ClF2N3O2Purity:98%Color and Shape:SolidMolecular weight:455.88Tinlorafenib
CAS:<p>Tinlorafenib (PF-07284890), a BRAFV600E/K inhibitor, is oral & CNS-permeable, used for BRAF-linked CNS tumors. IC50: 4.25/2.7 nM.</p>Formula:C19H19ClF2N4O3SColor and Shape:SolidMolecular weight:456.89
