Järvinen T - Search Results

1

Characterization of the sulfhydryl-sensitive site in the enzyme responsible for hydrolysis of 2-arachidonoyl-glycerol in rat cerebellar membranes.

Saario SM, Salo OM, Nevalainen T, Poso A, Laitinen JT, Järvinen T, Niemi R. Saario SM, et al. Among authors: jarvinen t. Chem Biol. 2005 Jun;12(6):649-56. doi: 10.1016/j.chembiol.2005.04.013. Chem Biol. 2005. PMID: 15975510

2

Synthesis and CB1 receptor activities of dimethylheptyl derivatives of 2-arachidonoyl glycerol (2-AG) and 2-arachidonyl glyceryl ether (2-AGE).

Parkkari T, Salo OM, Huttunen KM, Savinainen JR, Laitinen JT, Poso A, Nevalainen T, Järvinen T. Parkkari T, et al. Among authors: jarvinen t. Bioorg Med Chem. 2006 Apr 15;14(8):2850-8. doi: 10.1016/j.bmc.2005.12.007. Epub 2006 Jan 5. Bioorg Med Chem. 2006. PMID: 16403642

3

3D-QSAR studies on cannabinoid CB1 receptor agonists: G-protein activation as biological data.

Salo OM, Savinainen JR, Parkkari T, Nevalainen T, Lahtela-Kakkonen M, Gynther J, Laitinen JT, Järvinen T, Poso A. Salo OM, et al. Among authors: jarvinen t. J Med Chem. 2006 Jan 26;49(2):554-66. doi: 10.1021/jm0505157. J Med Chem. 2006. PMID: 16420041

4

Alpha-methylated derivatives of 2-arachidonoyl glycerol: synthesis, CB1 receptor activity, and enzymatic stability.

Parkkari T, Myllymäki M, Savinainen JR, Saario SM, Castillo-Meléndez JA, Laitinen JT, Nevalainen T, Koskinen AM, Järvinen T. Parkkari T, et al. Among authors: jarvinen t. Bioorg Med Chem Lett. 2006 May 1;16(9):2437-40. doi: 10.1016/j.bmcl.2006.01.101. Epub 2006 Feb 8. Bioorg Med Chem Lett. 2006. PMID: 16466915

5

Synthesis, cannabinoid receptor activity, and enzymatic stability of reversed amide derivatives of arachidonoyl ethanolamide.

Parkkari T, Savinainen JR, Raitio KH, Saario SM, Matilainen L, Sirviö T, Laitinen JT, Nevalainen T, Niemi R, Järvinen T. Parkkari T, et al. Among authors: jarvinen t. Bioorg Med Chem. 2006 Aug 1;14(15):5252-8. doi: 10.1016/j.bmc.2006.03.051. Epub 2006 Apr 27. Bioorg Med Chem. 2006. PMID: 16644227

6

Fatty acid amide hydrolase inhibitors from virtual screening of the endocannabinoid system.

Saario SM, Poso A, Juvonen RO, Järvinen T, Salo-Ahen OM. Saario SM, et al. Among authors: jarvinen t. J Med Chem. 2006 Jul 27;49(15):4650-6. doi: 10.1021/jm060394q. J Med Chem. 2006. PMID: 16854070

7

URB754 has no effect on the hydrolysis or signaling capacity of 2-AG in the rat brain.

Saario SM, Palomäki V, Lehtonen M, Nevalainen T, Järvinen T, Laitinen JT. Saario SM, et al. Among authors: jarvinen t. Chem Biol. 2006 Aug;13(8):811-4. doi: 10.1016/j.chembiol.2006.07.008. Chem Biol. 2006. PMID: 16931330

8

Design, synthesis, and in vitro evaluation of carbamate derivatives of 2-benzoxazolyl- and 2-benzothiazolyl-(3-hydroxyphenyl)-methanones as novel fatty acid amide hydrolase inhibitors.

Myllymäki MJ, Saario SM, Kataja AO, Castillo-Melendez JA, Nevalainen T, Juvonen RO, Järvinen T, Koskinen AM. Myllymäki MJ, et al. Among authors: jarvinen t. J Med Chem. 2007 Aug 23;50(17):4236-42. doi: 10.1021/jm070501w. Epub 2007 Aug 1. J Med Chem. 2007. PMID: 17665899 Free article.

9

Monoglyceride lipase-like enzymatic activity is responsible for hydrolysis of 2-arachidonoylglycerol in rat cerebellar membranes.

Saario SM, Savinainen JR, Laitinen JT, Järvinen T, Niemi R. Saario SM, et al. Among authors: jarvinen t. Biochem Pharmacol. 2004 Apr 1;67(7):1381-7. doi: 10.1016/j.bcp.2003.12.003. Biochem Pharmacol. 2004. PMID: 15013854

10

Synthesis and CB1 receptor activities of novel arachidonyl alcohol derivatives.

Parkkari T, Savinainen JR, Rauhala AL, Tolonen TL, Nevalainen T, Laitinen JT, Gynther J, Järvinen T. Parkkari T, et al. Among authors: jarvinen t. Bioorg Med Chem Lett. 2004 Jun 21;14(12):3231-4. doi: 10.1016/j.bmcl.2004.03.093. Bioorg Med Chem Lett. 2004. PMID: 15149681

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