Vasudevan Anil, Conner Scott E, Gentles Robert G, Faghih Ramin, Liu Huaqing, Dwight Wesley, Ireland Lynne, Kang Chae Hee, Esbenshade Timothy A, Bennani Youssef L, Hancock Arthur A
Neuroscience Research, Global Pharmaceutical Research and Development, Abbott Laboratories, 100 Abbott Park Road, Abbott Park, IL 60031, USA.
Bioorg Med Chem Lett. 2002 Nov 4;12(21):3055-8. doi: 10.1016/s0960-894x(02)00685-6.
The synthesis and biological evaluation of novel antagonists of the rat H(3) receptor are described. These compounds differ from prototypical H(3) antagonists in that they do not contain an imidazole moiety, but rather a substituted aminopyrrolidine moiety. A systematic modification of the substituents on the aminopyrrolidine ring was performed using pre-formatted precursor sets, where applicable, to afford several compounds with high affinity and selectivity for the H(3) receptor.
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