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Published in Bioorganic & medicinal chemistry letters (15.02.2006)
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Heteroarylureas with fused bicyclic diamine cores as inhibitors of fatty acid amide hydrolase
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Published in Bioorganic & medicinal chemistry letters (15.10.2020)
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Inhibition of fatty acid amide hydrolase produces analgesia by multiple mechanisms
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The First Potent and Selective Non-Imidazole Human Histamine H4 Receptor Antagonists
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Published in Journal of medicinal chemistry (11.09.2003)
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Cloning and Functional Expression of the Human Histamine H3 Receptor
Lovenberg, T W, Roland, B L, Wilson, S J, Jiang, X, Pyati, J, Huvar, A, Jackson, M R, Erlander, M G
Published in Molecular pharmacology (01.06.1999)
Published in Molecular pharmacology (01.06.1999)
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Preparation and Biological Evaluation of Indole, Benzimidazole, and Thienopyrrole Piperazine Carboxamides: Potent Human Histamine H4 Antagonists
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Published in Journal of medicinal chemistry (29.12.2005)
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Heteroarylureas with spirocyclic diamine cores as inhibitors of fatty acid amide hydrolase
Keith, John M., Jones, William M., Pierce, Joan M., Seierstad, Mark, Palmer, James A., Webb, Michael, Karbarz, Mark J., Scott, Brian P., Wilson, Sandy J., Luo, Lin, Wennerholm, Michelle L., Chang, Leon, Brown, Sean M., Rizzolio, Michele, Rynberg, Raymond, Chaplan, Sandra R., Breitenbucher, J. Guy
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Heteroaryl urea inhibitors of fatty acid amide hydrolase: Structure–mutagenicity relationships for arylamine metabolites
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Published in Bioorganic & medicinal chemistry letters (15.12.2012)
Published in Bioorganic & medicinal chemistry letters (15.12.2012)
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1-Aryl-2-((6-aryl)pyrimidin-4-yl)amino)ethanols as competitive inhibitors of fatty acid amide hydrolase
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Published in Bioorganic & medicinal chemistry letters (01.03.2014)
Published in Bioorganic & medicinal chemistry letters (01.03.2014)
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