Zobrazeno 1 - 10
of 23
pro vyhledávání: '"palmitoylisopropylamide"'
Autor:
Bashashati, M.1,2, Fichna, J.1,3, Piscitelli, F.4, Capasso, R.5, Izzo, A. A.6, Sibaev, A.7, Timmermans, J.‐P.8, Cenac, N.9,10,11, Vergnolle, N.9,10,11, Di Marzo, V.4, Storr, M.1,7,12,13 martin.storr@med.uni-muenchen.de
Publikováno v:
Neurogastroenterology & Motility. Dec2017, Vol. 29 Issue 12, pn/a-N.PAG. 10p.
Autor:
Jonsson, Kent-Olov
Anandamide (AEA) is an endogenous fatty acid which activates the same cannabinoid receptors as ∆9-tetrahydrocannabinol, the psychoactive substance in marijuana. In vivo, anandamide exerts a number of actions including effects upon pain and inflamma
Externí odkaz:
http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-445
Autor:
Jonsson, Kent-Olov, Andersson, Anna, Jacobsson, Stig O. P., Vandevoorde, Séverine, Lambert, Didier M., Fowler, Christopher J.
Publikováno v:
Archives of Toxicology; Apr2003, Vol. 77 Issue 4, p201-207, 7p
Publikováno v:
Life Sciences. Jan2006, Vol. 78 Issue 6, p598-606. 9p.
Autor:
Jonsson, Kent-Olov, Vandevoorde, Séverine, Lambert, Didier M, Tiger, Gunnar, Fowler, Christopher J
Publikováno v:
British Journal of Pharmacology; Aug2001, Vol. 133 Issue 8, p1263-1275, 13p
Autor:
Capasso, Raffaele, Matias, Isabel, Lutz, Beat, Borrelli, Francesca, Capasso, Francesco, Marsicano, Giovanni, Mascolo, Nicola, Petrosino, Stefania, Monory, Krisztina, Valenti, Marta, Di Marzo, Vincenzo, Izzo, Angelo A.
Publikováno v:
Gastroenterology (00165085); Sep2005, Vol. 129 Issue 3, p941-951, 11p
Autor:
Smart, Darren1, Jonsson, Kent-Olov2, Lambert, Didier M.3, Fowler, Christopher J.2 cf@pharm.umu.se, Vandevoorde, Séverine3, Vandevoorde, Séverine (AUTHOR)
Publikováno v:
British Journal of Pharmacology. Jun2002, Vol. 136 Issue 3, p452-458. 7p. 4 Graphs.
Publikováno v:
Life Sciences. 78:598-606
In a recent study so far published in abstract form, it was reported that the CB(2) receptor selective agonist AM1241 diminishes oedema produced as a result of mast cell degranulation in vivo. It is, however, not known whether other structurally diff
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::69ead50b98b0c158da16dbbb89ae0772
https://doi.org/10.1016/j.lfs.2005.05.059
https://doi.org/10.1016/j.lfs.2005.05.059
Autor:
Kent-Olov Jonsson, Stig O. P. Jacobsson, Didier M. Lambert, Séverine Vandevoorde, Anna Andersson, Christopher J. Fowler
Publikováno v:
Archives of Toxicology. 77:201-207
AM404 [ N-(4-hydroxyphenyl)arachidonylamide] and VDM 11 [(5 Z,8 Z,11 Z,14 Z)- N-(4-hydroxy-2-methylphenyl)-5,8,11,14-eicosatetraenamide] are commonly used to prevent the cellular accumulation of the endocannabinoid anandamide, and thereby to potentia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eec294e91b3c6bff0d54f98a2d5fa931
https://doi.org/10.1007/s00204-002-0435-6
https://doi.org/10.1007/s00204-002-0435-6
Autor:
Christopher J. Fowler, Didier M. Lambert, Séverine Vandevoorde, Gunnar Tiger, Kent-Olov Jonsson
Publikováno v:
British Journal of Pharmacology. 133:1263-1275
1 The ability of a series of homologues and analogues of palmitoylethanolamide to inhibit the uptake and fatty acid amidohydrolase (FAAH)-catalysed hydrolysis of [H-3]-anandamide ([H-3]-AEA) has been investigated. 2 Palmitoylethanolamide and homologu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7b9bd5851c27c9f94fbf83d2a3576ea0
https://doi.org/10.1038/sj.bjp.0704199
https://doi.org/10.1038/sj.bjp.0704199