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PUBMED FOR HANDHELDS

Journal Abstract Search


240 related items for PubMed ID: 23488865

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  • 22. Application of computational methods to the design of fatty acid amide hydrolase (FAAH) inhibitors based on a carbamic template structure.
    Lodola A, Rivara S, Mor M.
    Adv Protein Chem Struct Biol; 2011; 85():1-26. PubMed ID: 21920320
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  • 24. Enol carbamates as inhibitors of fatty acid amide hydrolase (FAAH) endowed with high selectivity for FAAH over the other targets of the endocannabinoid system.
    Gattinoni S, De Simone C, Dallavalle S, Fezza F, Nannei R, Amadio D, Minetti P, Quattrociocchi G, Caprioli A, Borsini F, Cabri W, Penco S, Merlini L, Maccarrone M.
    ChemMedChem; 2010 Mar 01; 5(3):357-60. PubMed ID: 20112328
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  • 31. Membrane lipids are key modulators of the endocannabinoid-hydrolase FAAH.
    Dainese E, De Fabritiis G, Sabatucci A, Oddi S, Angelucci CB, Di Pancrazio C, Giorgino T, Stanley N, Del Carlo M, Cravatt BF, Maccarrone M.
    Biochem J; 2014 Feb 01; 457(3):463-72. PubMed ID: 24215562
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  • 34. 1,3,4-Oxadiazol-2-ones as fatty-acid amide hydrolase and monoacylglycerol lipase inhibitors: Synthesis, in vitro evaluation and insight into potency and selectivity determinants by molecular modelling.
    Käsnänen H, Minkkilä A, Taupila S, Patel JZ, Parkkari T, Lahtela-Kakkonen M, Saario SM, Nevalainen T, Poso A.
    Eur J Pharm Sci; 2013 Jun 14; 49(3):423-33. PubMed ID: 23557840
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  • 35. Novel mechanistic class of fatty acid amide hydrolase inhibitors with remarkable selectivity.
    Ahn K, Johnson DS, Fitzgerald LR, Liimatta M, Arendse A, Stevenson T, Lund ET, Nugent RA, Nomanbhoy TK, Alexander JP, Cravatt BF.
    Biochemistry; 2007 Nov 13; 46(45):13019-30. PubMed ID: 17949010
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  • 36. Mining biologically-active molecules for inhibitors of fatty acid amide hydrolase (FAAH): identification of phenmedipham and amperozide as FAAH inhibitors.
    Vincent F, Nguyen MT, Emerling DE, Kelly MG, Duncton MA.
    Bioorg Med Chem Lett; 2009 Dec 01; 19(23):6793-6. PubMed ID: 19850474
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  • 37. The fatty acid amide hydrolase (FAAH).
    Ueda N, Puffenbarger RA, Yamamoto S, Deutsch DG.
    Chem Phys Lipids; 2000 Nov 01; 108(1-2):107-21. PubMed ID: 11106785
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  • 38. Reversible inhibitors of fatty acid amide hydrolase that promote analgesia: evidence for an unprecedented combination of potency and selectivity.
    Lichtman AH, Leung D, Shelton CC, Saghatelian A, Hardouin C, Boger DL, Cravatt BF.
    J Pharmacol Exp Ther; 2004 Nov 01; 311(2):441-8. PubMed ID: 15229230
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  • 39. A high throughput fluorescent assay for measuring the activity of fatty acid amide hydrolase.
    Kage KL, Richardson PL, Traphagen L, Severin J, Pereda-Lopez A, Lubben T, Davis-Taber R, Vos MH, Bartley D, Walter K, Harlan J, Solomon L, Warrior U, Holzman TF, Faltynek C, Surowy CS, Scott VE.
    J Neurosci Methods; 2007 Mar 30; 161(1):47-54. PubMed ID: 17083980
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