Journal of Medicinal Chemistry 2003-09-11

The first potent and selective non-imidazole human histamine H4 receptor antagonists.

Jill A Jablonowski, Cheryl A Grice, Wenying Chai, Curt A Dvorak, Jennifer D Venable, Annette K Kwok, Kiev S Ly, Jianmei Wei, Sherry M Baker, Pragnya J Desai, Wen Jiang, Sandy J Wilson, Robin L Thurmond, Lars Karlsson, James P Edwards, Timothy W Lovenberg, Nicholas I Carruthers

Index: J. Med. Chem. 46 , 3957-3960, (2003)

Full Text: HTML

Abstract

Following the discovery of the human histamine H4 receptor, a high throughput screen of our corporate compound collection identified compound 6 as a potential lead. Investigation of the SAR resulted in the discovery of novel compounds 10e and 10l, which are the first potent and selective histamine H4 receptor antagonists to be described.

Related Compounds

Structure Name/CAS No. Articles
JNJ-7777120 Structure JNJ-7777120
CAS:459168-41-3
5-Methyl-1H-indole-2-carboxylic acid Structure 5-Methyl-1H-indole-2-carboxylic acid
CAS:10241-97-1