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2-Arachidonoylglycerol was a Natural sciences good articles nominee, but did not meet the good article criteria at the time. There may be suggestions below for improving the article. Once these issues have been addressed, the article can be renominated. Editors may also seek a reassessment of the decision if they believe there was a mistake. | ||||||||||
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The text is a simple copy from http://www.caymanchem.com/app/template/Product.vm/catalog/62160. Someone should change it. —Preceding unsigned comment added by 82.166.182.11 ( talk) 16:35, 3 November 2007 (UTC)
The IUPAC name is for a carboxylate group but the article is for the di-carboxylic acid. is there a reason for this?-- ChemSpiderMan ( talk) 23:58, 5 January 2008 (UTC)
Sorry...I misread the structure..I reworked the structure and suggest the actual IUPAC Name is: 1,3-Dihydroxy-2-propanyl (5Z,8Z,11Z,14Z)-5,8,11,14-icosatetraenoate If you agree I'll let you change it.-- ChemSpiderMan ( talk) 04:35, 6 January 2008 (UTC)
Is paternal bovine different than maternal bovine milk? Shjacks45 ( talk) 10:23, 15 July 2008 (UTC)
Erm... I understand that this chemical is basically a neurotransmitter, but what does it actually do? Would anyone be willing to tell me or point me to a link that explains it in terms a high school C-grade physiology student could understand? EvangelionUnit01 ( talk) 22:13, 30 March 2011 (UTC)
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Reviewer: Sasata ( talk) 16:28, 8 June 2011 (UTC)
I will review this article; will have comments up here in a day or two. Sasata ( talk) 16:28, 8 June 2011 (UTC)
Someone inserted - with a couple of typos - the following reference nº 17 in this page:
Köfalvi, Attila (2008). Cannabinoids and the Brain. New York City: Axel Springer AG. p. 15. ISBN 978-0-387-74348-6. "2-Arachidonoylglycerol can be synthesized from arachidonic acid-containing diacylglycerol derived from increaded inositol phospholid metabolism by the action of a diacylglycerol lipase. 2-Arachidonoylglycerol can also be formed via other pathways such as the hydrolysis of the diaclygly derived from PC and phosphatidic acid by the action of a diacyglycerol lipase and the hydrolysis of arachidonic acid-containing lysophosphatidic acid by the action of a phosphatase. The relative importance of these pathways may depend on the types of cells and stimuli."
This happened without my consent and since it contains an excerpt from the book (which was transcribed with typos), I now make an attempt to delete the reference in question. The author of this text was not me but Dr Takayuki Sugiura from the Teikyo University.
Please do not reinsert text like this from my book, instead, try to look up the original report. Thank you! — Preceding unsigned comment added by Akofalvi ( talk • contribs) 20:03, 10 September 2015 (UTC)
This article is rated B-class on Wikipedia's
content assessment scale. It is of interest to the following WikiProjects: | |||||||||||||||||||||
|
2-Arachidonoylglycerol was a Natural sciences good articles nominee, but did not meet the good article criteria at the time. There may be suggestions below for improving the article. Once these issues have been addressed, the article can be renominated. Editors may also seek a reassessment of the decision if they believe there was a mistake. | ||||||||||
|
The text is a simple copy from http://www.caymanchem.com/app/template/Product.vm/catalog/62160. Someone should change it. —Preceding unsigned comment added by 82.166.182.11 ( talk) 16:35, 3 November 2007 (UTC)
The IUPAC name is for a carboxylate group but the article is for the di-carboxylic acid. is there a reason for this?-- ChemSpiderMan ( talk) 23:58, 5 January 2008 (UTC)
Sorry...I misread the structure..I reworked the structure and suggest the actual IUPAC Name is: 1,3-Dihydroxy-2-propanyl (5Z,8Z,11Z,14Z)-5,8,11,14-icosatetraenoate If you agree I'll let you change it.-- ChemSpiderMan ( talk) 04:35, 6 January 2008 (UTC)
Is paternal bovine different than maternal bovine milk? Shjacks45 ( talk) 10:23, 15 July 2008 (UTC)
Erm... I understand that this chemical is basically a neurotransmitter, but what does it actually do? Would anyone be willing to tell me or point me to a link that explains it in terms a high school C-grade physiology student could understand? EvangelionUnit01 ( talk) 22:13, 30 March 2011 (UTC)
GA toolbox |
---|
Reviewing |
Reviewer: Sasata ( talk) 16:28, 8 June 2011 (UTC)
I will review this article; will have comments up here in a day or two. Sasata ( talk) 16:28, 8 June 2011 (UTC)
Someone inserted - with a couple of typos - the following reference nº 17 in this page:
Köfalvi, Attila (2008). Cannabinoids and the Brain. New York City: Axel Springer AG. p. 15. ISBN 978-0-387-74348-6. "2-Arachidonoylglycerol can be synthesized from arachidonic acid-containing diacylglycerol derived from increaded inositol phospholid metabolism by the action of a diacylglycerol lipase. 2-Arachidonoylglycerol can also be formed via other pathways such as the hydrolysis of the diaclygly derived from PC and phosphatidic acid by the action of a diacyglycerol lipase and the hydrolysis of arachidonic acid-containing lysophosphatidic acid by the action of a phosphatase. The relative importance of these pathways may depend on the types of cells and stimuli."
This happened without my consent and since it contains an excerpt from the book (which was transcribed with typos), I now make an attempt to delete the reference in question. The author of this text was not me but Dr Takayuki Sugiura from the Teikyo University.
Please do not reinsert text like this from my book, instead, try to look up the original report. Thank you! — Preceding unsigned comment added by Akofalvi ( talk • contribs) 20:03, 10 September 2015 (UTC)