900164-95-6Relevant articles and documents
Benzimidazole- and indole-substituted 1,3′-bipyrrolidine benzamides as histamine H3 receptor antagonists
Cole, Derek C.,Gross, Jonathan L.,Comery, Thomas A.,Aschmies, Suzan,Hirst, Warren D.,Kelley, Cody,Kim, Ji-In,Kubek, Katie,Ning, Xiaoping,Platt, Brian J.,Robichaud, Albert J.,Solvibile, William R.,Stock, Joseph R.,Tawa, Gregory,Williams, Marla J.,Ellingboe, John W.
scheme or table, p. 1237 - 1240 (2010/06/15)
Using a focused screen of biogenic amine compounds we identified a novel series of H3R antagonists. A preliminary SAR study led to reduction of MW while increasing binding affinity and potency. Optimization of the physical properties of the ser
NOVEL AZACYCLY-SUBSTITUTED ARYLTHIENOPYRIMIDINONES, PROCESS FOR THEIR PREPARATION AND THEIR USE AS MEDICAMENTS
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Page/Page column 88, (2008/06/13)
The invention relates to azacyclyl-substituted arylthienopyrimidinones and their derivatives of formula (I), and their physiologically tolerated salts and physiologically functional derivatives, their preparation, medicaments comprising at least one azacyclyl-substituted arylthienopyrimidinone of the invention or its derivative, and the use of the azacyclyl-substituted aryithienopyrimidinones of the invention and their derivatives as MCH antagonists.
ORGANIC COMPOUNDS
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Page/Page column 55, (2008/06/13)
A compound of formula (I) or stereoisomers or pharmaceutically acceptable salts thereof, and their preparation and use as pharmaceuticals (I) wherein R1 R2 R3, R4 and W are as defined herein.