Novel antiallergic and antiinflammatory agents. Part II: Synthesis and pharmacology of TYB-2285 and its related compounds

Abstract A series of m -bis(glycoloylamino)benzene derivatives was synthesized by treatment of the corresponding m -diaminobenzene derivatives with glycoloyl chloride derivatives in pyridine. Hydrolysis of acetyl compounds gave hydroxy derivatives, from which other acyl derivatives could be synthesized. These compounds were tested in the rat PCA (passive cutaneous anaphylaxis) assay by oral administration. Benzonitrile derivatives ( 4c , 5c , 6c , 4h , 5h ) exhibited notable inhibition in this assay. Compounds 5c and 6c also showed remarkable inhibition of eosinophil adhesion to TNF- (tumor necrosis factor) α-treated HUVEC (human umbilical vein endothelial cells) in the range of 10 −8 −10 −5 M. Compound 5c is now under investigation in Japan as TYB-2285 ( Fig. 1 Download high-res image (46KB) Download full-size image Fig. 1 . Structures of compounds 1 and 2 , DSCG, Lodoxamide ethyl and TYB-2285. ) for asthma and atopic dermatitis in phase II clinical studies.