نتایج جستجو برای: hydroxyphenyl arachidonamide am404

تعداد نتایج: 2515  

Journal: :Japanese journal of pharmacology 1979
W Tsukada Y Ryokawa H Tachizawa

It is well-known that prostaglandin (PG) synthetase inhibitors such as aspirin and indomethacin induce gastrointestinal ulcer both in experimental animals and humans. In addition, it has been reported that PG levels in the plasma and gastric juice of patients with ulcer are significantly lower than these levels in healthy subjects (1). On the other hand, PGE type PGs and their analogs are effec...

Journal: :Physical chemistry chemical physics : PCCP 2015
P Hemberger G da Silva A J Trevitt T Gerber A Bodi

We have investigated the thermal decomposition of the three hydroxyphenyl radicals (˙C6H4OH) in a heated microtubular reactor. Intermediates and products were identified isomer-selectively applying photoion mass-selected threshold photoelectron spectroscopy with vacuum ultraviolet synchrotron radiation. Similarly to the phenoxy radical (C6H5-O˙), hydroxyphenyl decomposition yields cyclopentadie...

Journal: :Physical chemistry chemical physics : PCCP 2016
Matthew B Prendergast Benjamin B Kirk John D Savee David L Osborn Craig A Taatjes Kye-Simeon Masters Stephen J Blanksby Gabriel da Silva Adam J Trevitt

Gas-phase product detection studies of o-hydroxyphenyl radical and O2 are reported at 373, 500, and 600 K, at 4 Torr (533.3 Pa), using VUV time-resolved synchrotron photoionisation mass spectrometry. The dominant products are assigned as o-benzoquinone (C6H4O2, m/z 108) and cyclopentadienone (C5H4O, m/z 80). It is concluded that cyclopentadienone forms as a secondary product from prompt decompo...

Journal: :Bioorganic & medicinal chemistry letters 2003
Yoffi Segall Gary B Quistad Daniel K Nomura John E Casida

Arachidonylsulfonyl fluoride (3), reported here for the first time, is similar in potency to its known methyl arachidonylfluorophosphonate (2) analogue as an inhibitor of mouse brain fatty acid amide hydrolase activity (IC(50) 0.1 nM) and cannabinoid CB1 agonist [3H]CP 55,940 binding (IC(50) 304-530 nM). Interestingly, 3 is much more selective than 2 as an inhibitor for fatty acid amide hydrola...

Journal: :The Journal of neuroscience : the official journal of the Society for Neuroscience 2003
Ya-Chun Huang Su-Jane Wang Lih-Chu Chiou Po-Wu Gean

The amygdala is thought to mediate memory consolidation of amphetamine-induced conditioned place preference, a behavioral paradigm that requires memory for an association between environmental cues and the affective state produced by the drug treatment. Here we show that amphetamine induces long-term synaptic depression (LTD) in the amygdala. Amphetamine LTD is not affected by dopamine, seroton...

Journal: :Pharmacological reports : PR 2006
Maria Rutkowska Joanna Jamontt Halina Gliniak

Several pieces of anatomical, biochemical and pharmacological evidence indicate that the endocannabinoid system via CB1 receptors is implicated in the control of emotional behavior. However, previous studies have reported unclear and contradictory results concerning the role of cannabinoids in anxiety. The aim of the present study was to examine the influence of the cannabinoid agonist WIN 55,2...

Background and Aims: Hypertyrosinemia type 3 (HT3) is an inherited error in tyrosine metabolism caused by a mutation in the 4-hydroxyphenylpyruvate dioxygenase (HPD) gene. Here we report a one and half-year-old girl infant who was diagnosed based on increased serum tyrosine levels and increased urinary excretion of p-hydroxyphenyl derivatives. Materials and Methods: The proband was one and ha...

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