
JNK
As JNKs (c-Jun N-terminal kinases) são um subgrupo da família MAPK que respondem a estímulos de estresse, como citocinas, radiação ultravioleta e choque térmico, e estão envolvidas no controle da apoptose, inflamação e respostas imunológicas. A sinalização JNK é crucial para a regulação das respostas celulares ao estresse e tem sido implicada em várias doenças, incluindo distúrbios neurodegenerativos, câncer e condições inflamatórias. Na CymitQuimica, oferecemos uma variedade de moduladores da via JNK para apoiar sua pesquisa em sinalização de estresse, apoptose e patologia de doenças.
Foram encontrados 105 produtos de "JNK"
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JNK-IN-21
CAS:JNK-IN-21 (Compound 62) is an inhibitor of JNK-1.Fórmula:C19H16N2O2SCor e Forma:SolidPeso molecular:336.408JAK3-IN-13
JAK3-IN-13: Oral JAK3 inhibitor, selective & potent. Acts on NK1, JNK2, JNK3, Tyk2. Anti-tumor. IC50: JNK3, 8 nM; Tyk2, 365 nM; JNK2, 2039 nM; NK1, 4728 nM.Fórmula:C25H33ClN6O5Cor e Forma:SolidPeso molecular:533.02Nitric oxide production-IN-2
CAS:TLR4/JNK/NF-κB-IN-1 (Racemic-11k) is an inhibitor of TLR4, JNK, and NF-κB. It suppresses NO production in LPS-stimulated RAW264.7 cells with an IC50 of 23.2 µM. By inhibiting TLR4 expression and reducing JNK phosphorylation, TLR4/JNK/NF-κB-IN-1 prevents NF-κB activation. This leads to a decrease in the transcription of inflammation-related genes, reducing the expression of iNOS and COX-2, and the production of inflammatory mediators such as NO, PGE2, and TNF-α, thereby exhibiting anti-inflammatory activity. TLR4/JNK/NF-κB-IN-1 holds potential in the study of inflammatory diseases, including rheumatoid arthritis and various other inflammatory conditions.Fórmula:C23H20O3Cor e Forma:SolidPeso molecular:344.403JD118
CAS:<p>JD118 is an inhibitor of JNK. It effectively suppresses the activity of JNK1 and the expression of cJun (1 - 135).</p>Fórmula:C13H12N4S2Cor e Forma:SolidPeso molecular:288.391JNK-1-IN-5
CAS:JNK-1-IN-5 (Compound 14) is a potent JNK1 inhibitor with sub-nanomolar efficacy. It effectively inhibits TGF-β-induced epithelial-mesenchymal transition and shows promise for research targeting JNK1 as an anti-pulmonary fibrosis agent.Fórmula:C23H21BrN6O3Cor e Forma:SolidPeso molecular:509.355

