165 related articles for article (PubMed ID: 26850005)
21. Biaryl tetrazolyl ureas as inhibitors of endocannabinoid metabolism: modulation at the N-portion and distal phenyl ring.
Ortar G; Morera E; De Petrocellis L; Ligresti A; Schiano Moriello A; Morera L; Nalli M; Ragno R; Pirolli A; Di Marzo V
Eur J Med Chem; 2013 May; 63():118-32. PubMed ID: 23474898
[TBL] [Abstract][Full Text] [Related]
22. Effects of endocannabinoid and endovanilloid systems on aversive memory extinction.
Laricchiuta D; Centonze D; Petrosini L
Behav Brain Res; 2013 Nov; 256():101-7. PubMed ID: 23948212
[TBL] [Abstract][Full Text] [Related]
23. Structure-activity relationship for aryl and heteroaryl boronic acid inhibitors of hormone-sensitive lipase.
Ebdrup S; Jacobsen P; Farrington AD; Vedsø P
Bioorg Med Chem; 2005 Mar; 13(6):2305-12. PubMed ID: 15727879
[TBL] [Abstract][Full Text] [Related]
24. 1-(5-Carboxyindazol-1-yl)propan-2-ones as dual inhibitors of cytosolic phospholipase A
Althaus J; Hake T; Hanekamp W; Lehr M
J Enzyme Inhib Med Chem; 2016; 31(sup1):131-140. PubMed ID: 27162011
[TBL] [Abstract][Full Text] [Related]
25. Paracetamol analogues conjugated by FAAH induce TRPV1-mediated antinociception without causing acute liver toxicity.
Å Nilsson JL; Mallet C; Shionoya K; Blomgren A; Sundin AP; Grundemar L; Boudieu L; Blomqvist A; Eschalier A; Nilsson UJ; Zygmunt PM
Eur J Med Chem; 2021 Mar; 213():113042. PubMed ID: 33257173
[TBL] [Abstract][Full Text] [Related]
26. Fatty acid amide hydrolase inhibitors. 3: tetra-substituted azetidine ureas with in vivo activity.
Roughley SD; Browne H; Macias AT; Benwell K; Brooks T; D'Alessandro J; Daniels Z; Dugdale S; Francis G; Gibbons B; Hart T; Haymes T; Kennett G; Lightowler S; Matassova N; Mansell H; Merrett A; Misra A; Padfield A; Parsons R; Pratt R; Robertson A; Simmonite H; Tan K; Walls SB; Wong M
Bioorg Med Chem Lett; 2012 Jan; 22(2):901-6. PubMed ID: 22209458
[TBL] [Abstract][Full Text] [Related]
27. Discovery of Uracil Derivatives as Potent Inhibitors of Fatty Acid Amide Hydrolase.
Qiu Y; Zhang Y; Li Y; Ren J
Molecules; 2016 Feb; 21(2):. PubMed ID: 26901181
[TBL] [Abstract][Full Text] [Related]
28. 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
[TBL] [Abstract][Full Text] [Related]
29. Synthesis and evaluation of paracetamol esters as novel fatty acid amide hydrolase inhibitors.
Onnis V; Congiu C; Björklund E; Hempel F; Söderström E; Fowler CJ
J Med Chem; 2010 Mar; 53(5):2286-98. PubMed ID: 20143779
[TBL] [Abstract][Full Text] [Related]
30. Benzylamides and piperazinoarylamides of ibuprofen as fatty acid amide hydrolase inhibitors.
Deplano A; Cipriano M; Moraca F; Novellino E; Catalanotti B; Fowler CJ; Onnis V
J Enzyme Inhib Med Chem; 2019 Dec; 34(1):562-576. PubMed ID: 30688118
[TBL] [Abstract][Full Text] [Related]
31. A novel scintillation proximity assay for fatty acid amide hydrolase compatible with inhibitor screening.
Wang Y; Xu J; Uveges A; Ramarao MK; Rogers KE; Jones PG
Anal Biochem; 2006 Jul; 354(1):35-42. PubMed ID: 16707086
[TBL] [Abstract][Full Text] [Related]
32. 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; 19(23):6793-6. PubMed ID: 19850474
[TBL] [Abstract][Full Text] [Related]
33. Involvement of the endocannabinoid system in retinal damage after high intraocular pressure-induced ischemia in rats.
Nucci C; Gasperi V; Tartaglione R; Cerulli A; Terrinoni A; Bari M; De Simone C; Agrò AF; Morrone LA; Corasaniti MT; Bagetta G; Maccarrone M
Invest Ophthalmol Vis Sci; 2007 Jul; 48(7):2997-3004. PubMed ID: 17591864
[TBL] [Abstract][Full Text] [Related]
34. Identification of potent, noncovalent fatty acid amide hydrolase (FAAH) inhibitors.
Gustin DJ; Ma Z; Min X; Li Y; Hedberg C; Guimaraes C; Porter AC; Lindstrom M; Lester-Zeiner D; Xu G; Carlson TJ; Xiao S; Meleza C; Connors R; Wang Z; Kayser F
Bioorg Med Chem Lett; 2011 Apr; 21(8):2492-6. PubMed ID: 21392988
[TBL] [Abstract][Full Text] [Related]
35. 1-Heteroarylpropan-2-ones as inhibitors of fatty acid amide hydrolase: Studies on structure-activity relationships and metabolic stability.
Zahov S; Garzinsky D; Hanekamp W; Lehr M
Bioorg Med Chem; 2017 Feb; 25(3):825-837. PubMed ID: 27989417
[TBL] [Abstract][Full Text] [Related]
36. Scaffold hopping-guided design of some isatin based rigid analogs as fatty acid amide hydrolase inhibitors: Synthesis and evaluation.
Jaiswal S; Tripathi RKP; Ayyannan SR
Biomed Pharmacother; 2018 Nov; 107():1611-1623. PubMed ID: 30257379
[TBL] [Abstract][Full Text] [Related]
37. Further exploration of the structure-activity relationship of dual soluble epoxide hydrolase/fatty acid amide hydrolase inhibitors.
Wilt S; Kodani S; Valencia L; Hudson PK; Sanchez S; Quintana T; Morisseau C; Hammock BD; Kandasamy R; Pecic S
Bioorg Med Chem; 2021 Dec; 51():116507. PubMed ID: 34794001
[TBL] [Abstract][Full Text] [Related]
38. Characterization of the endocannabinoid system in human spermatozoa and involvement of transient receptor potential vanilloid 1 receptor in their fertilizing ability.
Francavilla F; Battista N; Barbonetti A; Vassallo MR; Rapino C; Antonangelo C; Pasquariello N; Catanzaro G; Barboni B; Maccarrone M
Endocrinology; 2009 Oct; 150(10):4692-700. PubMed ID: 19608651
[TBL] [Abstract][Full Text] [Related]
39. Macamides and their synthetic analogs: evaluation of in vitro FAAH inhibition.
Wu H; Kelley CJ; Pino-Figueroa A; Vu HD; Maher TJ
Bioorg Med Chem; 2013 Sep; 21(17):5188-97. PubMed ID: 23891163
[TBL] [Abstract][Full Text] [Related]
40. 1-Indol-1-yl-propan-2-ones and related heterocyclic compounds as dual inhibitors of cytosolic phospholipase A(2)alpha and fatty acid amide hydrolase.
Forster L; Ludwig J; Kaptur M; Bovens S; Elfringhoff AS; Holtfrerich A; Lehr M
Bioorg Med Chem; 2010 Jan; 18(2):945-52. PubMed ID: 20005725
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
