1350411-35-6Relevant articles and documents
Design and synthesis of a novel series of histamine H3 receptor antagonists through a scaffold hopping strategy
Gao, Zhongli,Hurst, William J.,Hall, Daniel,Hartung, Ryan,Reynolds, William,Kang, Jiesheng,Nagorny, Raisa,Hendrix, James A.,George, Pascal G.
, p. 429 - 438 (2015/01/30)
Lead compounds 5-fluoro-2-methyl-N-[2-methyl-4-(2-methyl-[1,3′]bipyrrolidinyl-1′-yl)-phenyl]-benzamide (1), tetrahydro-pyran-4-carboxylic acid [((2S,3′S)-2-methyl-[1,3′]bipyrrolidinyl-1′-yl)-phenyl]-amide (2), and 3,5-dimethyl-isoxazole-4-carboxylic acid