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Journal of Medicinal Chemistry|January 20, 2006
3D-QSAR studies on cannabinoid CB1 receptor agonists: G-protein activation as biological dataOuti M H Salo, Juha R Savinainen, Teija Parkkari, et al.Journal of Medicinal Chemistry|August 2, 2007
Design, synthesis, and in vitro evaluation of carbamate derivatives of 2-benzoxazolyl- and 2-benzothiazolyl-(3-hydroxyphenyl)-methanones as novel fatty acid amide hydrolase inhibitorsMikko J Myllymäki, Susanna M Saario, Antti O Kataja, et al.Bioorganic & Medicinal Chemistry|April 29, 2006
Synthesis, cannabinoid receptor activity, and enzymatic stability of reversed amide derivatives of arachidonoyl ethanolamideTeija Parkkari, Juha R Savinainen, Katri H Raitio, et al.Bioorganic & Medicinal Chemistry Letters|February 10, 2006
Alpha-methylated derivatives of 2-arachidonoyl glycerol: synthesis, CB1 receptor activity, and enzymatic stabilityTeija Parkkari, Mikko Myllymäki, Juha R Savinainen, et al.The Journal of Pharmacology and Experimental Therapeutics|July 25, 2016
In Vivo Characterization of the Ultrapotent Monoacylglycerol Lipase Inhibitor {4-[bis-(benzo[d][1,3]dioxol-5-yl)methyl]-piperidin-1-yl}(1H-1,2,4-triazol-1-yl)methanone (JJKK-048)Niina Aaltonen, Ewa Kedzierska, Jolanta Orzelska-Górka, et al.Molecular Pharmacology|August 21, 2014
Robust hydrolysis of prostaglandin glycerol esters by human monoacylglycerol lipase (MAGL)Juha R Savinainen, Emilia Kansanen, Tatu Pantsar, et al.Plos One|June 1, 2014
Discovery of triterpenoids as reversible inhibitors of α/β-hydrolase domain containing 12 (ABHD12)Teija Parkkari, Raisa Haavikko, Tuomo Laitinen, et al.Journal of Medicinal Chemistry|October 3, 2013
Chiral 1,3,4-oxadiazol-2-ones as highly selective FAAH inhibitorsJayendra Z Patel, Teija Parkkari, Tuomo Laitinen, et al.Chemistry & Biology|March 26, 2013
Piperazine and piperidine triazole ureas as ultrapotent and highly selective inhibitors of monoacylglycerol lipaseNiina Aaltonen, Juha R Savinainen, Casandra Riera Ribas, et al.Pageof 6