847234-41-7Relevant academic research and scientific papers
Substituted indole-1-acetic acids as potent and selective CRTh2 antagonists-discovery of AZD1981
Luker, Tim,Bonnert, Roger,Brough, Steve,Cook, Anthony R.,Dickinson, Mark R.,Dougall, Iain,Logan, Chris,Mohammeda, Rukhsana T.,Paine, Stuart,Sanganee, Hitesh J.,Sargent, Carol,Schmidt, Jerzy A.,Teague, Simon,Thom, Stephen
, p. 6288 - 6292 (2011/11/29)
Novel indole-3-thio-, 3-sulfonyl- and 3-oxy-aryl-1-acetic acids are reported which are potent, selective antagonists of the chemoattractant receptor-homologous expressed on Th2 lymphocytes receptor (CRTh2 or DP2). Optimization required maintenance of high
