[1]JournalofMedicinalChemistry,2005,vol.48,p.5966-5979
[2]Patent:EP1180518,2002,A1.Locationinpatent:Example19
[1]JournalofMedicinalChemistry,2005,vol.48,p.5966-5979
[1]JournalofMedicinalChemistry,2005,vol.48,p.5966-5979
[1]JournalofMedicinalChemistry,2005,vol.48,p.5966-5979
[1]JournalofMedicinalChemistry,2005,vol.48,p.5966-5979
Title: The p38alpha mitogen-activated protein kinase as a central nervous system drug discovery target.
Journal: BMC neuroscience 20080101
Title: Novel inhibitor of p38 MAP kinase as an anti-TNF-alpha drug: discovery of N-[4-[2-ethyl-4-(3-methylphenyl)-1,3-thiazol-5-yl]-2-pyridyl]benzamide (TAK-715) as a potent and orally active anti-rheumatoid arthritis agent.
Journal: Journal of medicinal chemistry 20050922
Title: Miwatashi S, et al. Novel inhibitor of p38 MAP kinase as an anti-TNF-alpha drug: discovery of N---ethyl-4-(3-methylphenyl)-1,3-thiazol-5-yl-2-pyridylbenzamide (TAK-715) as a potent and orally active anti-rheumatoid arthritis agent. J Med Chem, 2005, 48(19), 5966-5979.
Title: Verkaar F, et al. Inhibition of Wnt/β-catenin signaling by p38 MAP kinase inhibitors is explained by cross-reactivity with casein kinase Iδ/ɛ. Chem Biol, 2011, 18(4), 485-494.
Title: Huiwen Ren, et al. Inhibition of α1-adrenoceptor reduces TGF-β1-induced epithelial-to-mesenchymal transition and attenuates UUO-induced renal fibrosis in mice. FASEB J. 2020 Nov;34(11):14892-14904.