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 893 prodotti di "MAPK"
Ordinare per
Purezza (%)
0
100
|
0
|
50
|
90
|
95
|
100
KRAS G12D inhibitor 10
CAS:KRAS G12D inhibitor 10 targets KRAS G12D in cancer research (WO2021108683A1, compound 34).Formula:C33H41ClN8O2Colore e forma:SolidPeso molecolare:617.18GGTI-286
CAS:GGTI-286: GGTase I inhibitor, cell-permeable, IC50=2μM. Strongly blocks Rap1A geranylation; less effective on H-Ras, Ras4B IC50=1μM.Formula:C23H31N3O3SColore e forma:SolidPeso molecolare:429.58MCP110
CAS:MCP110 is an inhibitor of the interaction of Ras with Raf-1 and can be used in studies about the treatment of human tumors.Formula:C33H36N2O3Purezza:97.23%Colore e forma:OilPeso molecolare:508.65KYA1797
CAS:KYA1797 inhibits Wnt/ß-catenin, targeting axin, and promotes ß-catenin/Ras decay, halting APC/KRAS mutant CRC growth.Formula:C17H12N2O6S2Purezza:98%Colore e forma:SolidPeso molecolare:404.42RSK2-IN-2
CAS:<p>RSK2-IN-2 (Compound 25) is a reversible covalent inhibitor of the RPS6KA3 ( RSK2 ) kinase which also inhibits MSK1, MSK2, and RSK3 [1].</p>Formula:C16H11N5OColore e forma:SolidPeso molecolare:289.29GABAB receptor antagonist 1
CAS:(E)-GABAB receptor antagonist 1 decreases GABA-induced IP3 (inositol trisphosphate) production with IC50 of 37.9 μM.GABAB receptor antagonist 1 is a selectiveFormula:C18H24O4Purezza:98%Colore e forma:SolidPeso molecolare:304.38B-Raf IN 8
CAS:<p>B-Raf IN 8: strong B-Raf inhibitor (70.65 nM IC50); combats liver, colon, breast & prostate cancer with IC50s from 9.78 to 29.85 μM.</p>Formula:C18H17N3O2Colore e forma:SolidPeso molecolare:307.35HPK1-IN-24
CAS:<p>HPK1-IN-24 (example 51) has potential to be used in the cancer research which is an inhibitor of hematopoietic progenitor kinase 1 (HPK1) (Ki = 100 nM) [1].</p>Formula:C19H14FN5Colore e forma:SolidPeso molecolare:331.35UC-857993
CAS:UC-857993 is a selective SOS1-Ras inhibitor with a Kd of 14.7 μM that inhibits ERK, Ras, and reduces MEF growth.Formula:C25H22ClNO2Colore e forma:SolidPeso molecolare:403.9JNK3 inhibitor-2
CAS:<p>JNK3 inhibitor-2: selectively inhibits JNK3 (IC50 = 0.25 μM); less effective on JNK1/JNK2 (>100 μM); targets DDR1 and EGFR mutations.</p>Formula:C20H14N2O2Colore e forma:SolidPeso molecolare:314.34Tpl2 Kinase Inhibitor 1
CAS:Tpl2 Kinase Inhibitor 1 is an effective and selective Tpl2 inhibitor.Formula:C21H14ClFN6Purezza:98%Colore e forma:SolidPeso molecolare:404.83SX 011
CAS:SX 011 is a p38α inhibitor.Formula:C26H27ClFN3O3Purezza:98%Colore e forma:SolidPeso molecolare:483.96KRAS inhibitor-7
CAS:<p>KRAS inhibitor-7 is a potent KRAS G12C inhibitor.</p>Formula:C26H27ClF2N6O2Purezza:98%Colore e forma:SolidPeso molecolare:528.98HPK1-IN-25
CAS:HPK1-IN-25, an HPK1 inhibitor, IC50 129 nM, may aid cancer research.Formula:C23H25N5OColore e forma:SolidPeso molecolare:387.48KRAS G12C inhibitor 43
CAS:<p>KRAS G12C inhibitor 43 strongly blocks KRAS G12C, H358 cell growth (IC50: 0.001-1μM), less effective on A549, HCC cells (IC50>1μM).</p>Formula:C33H35N7O3Colore e forma:SolidPeso molecolare:577.68GGTI-286 hydrochloride
CAS:GGTI-286 HCl strongly inhibits GGTase I (IC50: 2 μM) and K-Ras4B farnesylation (IC50: 1 μM).Formula:C23H32ClN3O3SColore e forma:SolidPeso molecolare:466.04SMAP-2
CAS:SMAP-2: oral PP2A activator, targets Aα subunit, halts KRAS-mutant lung cancer growth.Formula:C27H27F3N2O4SPurezza:98%Colore e forma:SolidPeso molecolare:532.57HPK1-IN-26
CAS:HPK1-IN-26, from WO2021254118A1, is a potent dual HPK1/GLK inhibitor for studying animal infections.Formula:C19H21N5OSColore e forma:SolidPeso molecolare:367.47ZINC09659342
CAS:<p>ZINC09659342 (compound 13) is an inhibitor of Lbc-RhoA interaction (IC50: 3.6 μM).</p>Formula:C23H15F3N2O4Colore e forma:SolidPeso molecolare:440.37NSC-658497
CAS:NSC-658497 is a SOS1-Ras interaction inhibitor that acts by dose-dependently inhibiting SOS1 GEF activity.Formula:C20H10N2O6S2Purezza:98%Colore e forma:SolidPeso molecolare:438.43SR 3576
CAS:JNK3 inhibitor, potent and selectiveFormula:C27H27N5O5Purezza:98%Colore e forma:SolidPeso molecolare:501.53CAY10561
CAS:CAY10561: potent, selective ERK2 inhibitor (Ki=2nM); blocks cell proliferation; IC50 in COLO 205 cells: 0.54μM.Formula:C22H17Cl2FN4O2Colore e forma:SolidPeso molecolare:459.3KRAS G12C inhibitor 22
CAS:KRAS G12C inhibitor 22 is a KRAS G12C inhibitor.Formula:C32H41N7O2Colore e forma:SolidPeso molecolare:555.71Quazinone
CAS:Quazinone: PDE3 inhibitor, enhances heart muscle contractility, lowers blood pressure, and inhibits DNA synthesis in muscle cells. IC50 = 4.2 μM.Formula:C11H10ClN3OColore e forma:SolidPeso molecolare:235.67SB-747651A
CAS:SB-747651A: ATP-competitive MSK1 inhibitor (IC50=11nM), affects N-terminal domain, also hinders MSK2, PKA, PKB, RSK, p70S6K.Formula:C16H22N8OPurezza:98%Colore e forma:SolidPeso molecolare:342.4EO 1428
CAS:p38α and p38β2 inhibitorFormula:C20H16BrClN2OPurezza:98%Colore e forma:SolidPeso molecolare:415.71PD 334581
CAS:MEK1 inhibitorFormula:C20H19F3IN5O2Purezza:98%Colore e forma:SolidPeso molecolare:545.3p38α inhibitor 2
CAS:P38α Inhibitor 2, a potent and selective inhibitor of p38α MAPK, exhibits a pIC50 value of 9.6.Formula:C27H33N5O3Colore e forma:SolidPeso molecolare:475.58pan-KRAS-IN-16
CAS:3344 is an inhibitor of KRAS-effector interactions，with an affnity of 126nm.Formula:C24H26N2O3Purezza:98%Colore e forma:SolidPeso molecolare:390.47B-Raf IN 6
CAS:B-Raf IN 6: potent B-Raf kinase inhibitor, IC50 of 1.7 nM, doesn't target PXR, metabolically stable, potential in cancer research.Formula:C24H21F3N6O2S2Colore e forma:SolidPeso molecolare:546.59(R)-CE3F4
CAS:(R)-CE3F4 is a selective inhibitor of exchange protein directly activated by cAMP isoform 1 (Epac1)(IC50 of 4.2 μM),Formula:C11H10Br2FNOColore e forma:SolidPeso molecolare:351.01SR-3737
CAS:SR-3737 is potent both JNK3 and p38 inhibitor.Formula:C29H25FN4O4Purezza:98%Colore e forma:SolidPeso molecolare:512.53TOPK-p38/JNK-IN-1
CAS: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 NOFormula:C17H15F3N2O4Colore e forma:SolidPeso molecolare:368.31B-Raf IN 7
CAS:"B-Raf IN 7 inhibits B-Raf (IC50: 110.23 nM); fights colon, breast, liver, cervical, prostate cancers (IC50: 7.50-12.83 μM)."Formula:C15H16N6O3Colore e forma:SolidPeso molecolare:328.33KB-5246
CAS:KB-5246, displays antibacterial activities.is a tetracyclic quinolone.Formula:C18H17ClFN3O4SPurezza:98%Colore e forma:SolidPeso molecolare:425.86KRas G12C inhibitor 4
CAS:KRas G12C inhibitor 4 is a compound that inhibits KRas G12C.Formula:C33H38ClN7O2Purezza:98%Colore e forma:SolidPeso molecolare:600.15Avutometinib potassium
CAS:Avutometinib potassium, a MEKi, blocks Delta and Omicron infection in airway cells, potentially lessening disease severity.Formula:C21H17FKN5O5SColore e forma:SolidPeso molecolare:509.553,4-Dephostatin
CAS:3,4-Dephostatin is an inhibitor of the interactions of CFTR-associated ligand (CAL) and PSD-95/Dlg1/ZO-1 (PDZ) domain.Formula:C7H8N2O3Colore e forma:SolidPeso molecolare:168.15ERK5-IN-3
CAS:ERK5-IN-3 inhibits ERK5 strongly (IC50: 6 nM) and hampers Hela cell growth (IC50: 31 nM).Formula:C24H23Cl2FN4O2Colore e forma:SolidPeso molecolare:489.37Ras modulator-1
CAS:Ras modulator-1 is a modulator of Ras.Formula:C29H21N5O4SColore e forma:SolidPeso molecolare:535.57KRas G12C inhibitor 3
CAS:KRas G12C inhibitor 3 is a compound that inhibits KRas G12C.Formula:C32H36ClN7O2Purezza:98%Colore e forma:SolidPeso molecolare:586.13MW108
CAS:MW108 is an active site targeted, CNS-active, p38αMAPK inhibitor.Formula:C21H19ClN4Colore e forma:SolidPeso molecolare:362.86(S)-CCG-1423
(S)-CCG-1423, a stereoisomer, inhibits Rho to block myocardin-related transcription factor A & serum response signaling.Formula:C18H13ClF6N2O3Purezza:98%Colore e forma:SolidPeso molecolare:454.8K-Ras G12C-IN-3
CAS:K-Ras G12C-IN-3: novel, irreversible inhibitor of K-Ras G12C mutant protein for cancer treatment.Formula:C21H19Cl3N2O3Colore e forma:SolidPeso molecolare:453.75ML 3403
CAS:p38 MAPK inhibitor; IC50: 0.38μM. Reduces IL-1β & TNF-α release in PBMC assay; IC50: 0.039μM & 0.16μM.Formula:C23H21FN4SColore e forma:SolidPeso molecolare:404.5CCG-232601
CAS:CCG-232601 is a inhibitor of the Rho/MRTF/SRF transcriptional pathway.Formula:C24H20ClF2N3O2Purezza:98%Colore e forma:SolidPeso molecolare:455.88Tinlorafenib
CAS:Tinlorafenib (PF-07284890), a BRAFV600E/K inhibitor, is oral & CNS-permeable, used for BRAF-linked CNS tumors. IC50: 4.25/2.7 nM.Formula:C19H19ClF2N4O3SColore e forma:SolidPeso molecolare:456.89PHT-7.3
CAS:PHT-7.3 is a selective connector enhancer of kinase suppressor of Ras 1 (Cnk1) pleckstrin homology (PH) domain inhibitorFormula:C24H23N3O3SPurezza:98%Colore e forma:SolidPeso molecolare:433.52BRAF V600E/CRAF-IN-1
CAS:BRAF V600E/CRAF-IN-1: potent BRAF/CRAF inhibitor, induces cell cycle arrest and apoptosis in HCT-116 cells, promising for cancer research.Formula:C25H17F6N3O2Colore e forma:SolidPeso molecolare:505.41KRAS inhibitor-6
CAS:KRAS inhibitor-6 is a potent KRAS G12C inhibitor.Formula:C27H30ClF2N5O3Purezza:98%Colore e forma:SolidPeso molecolare:546.01
