Difference between revisions of "Template:Catecholamine and trace amine biosynthesis"

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imported>BrandonXLF
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imported>Seppi333
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{{annotation|{{if pagename|N-Methylphenethylamine=420|other=430}}|60|{{if pagename|N-Methylphenethylamine={{highlight|'''''N''-Methylphenethylamine'''}}|Trace amine={{highlight|[[N-Methylphenethylamine|''N''-Methylphenethylamine]]}}|other=[[N-Methylphenethylamine|''N''-Methylphenethylamine]]}}}}
 
{{annotation|440|150|{{if pagename|N-Methyltyramine={{highlight|'''''N''-Methyltyramine'''}}|Trace amine={{highlight|[[N-Methyltyramine|''N''-Methyltyramine]]}}|other=[[N-Methyltyramine|''N''-Methyltyramine]]}}}}
 
{{annotation|440|150|{{if pagename|N-Methyltyramine={{highlight|'''''N''-Methyltyramine'''}}|Trace amine={{highlight|[[N-Methyltyramine|''N''-Methyltyramine]]}}|other=[[N-Methyltyramine|''N''-Methyltyramine]]}}}}
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{{annotation|445|445|{{if pagename|Synephrine={{highlight|'''Synephrine'''}}|Trace amine={{highlight|[[Synephrine]]}}|other=[[Synephrine]]}}}}
 
{{annotation|445|445|{{if pagename|Synephrine={{highlight|'''Synephrine'''}}|Trace amine={{highlight|[[Synephrine]]}}|other=[[Synephrine]]}}}}
 
{{annotation|425|565|{{if pagename|3-Methoxytyramine={{highlight|'''3-Methoxytyramine'''}}|Trace amine={{highlight|[[3-Methoxytyramine]]}}|other=[[3-Methoxytyramine]]}}}}
 
{{annotation|425|565|{{if pagename|3-Methoxytyramine={{highlight|'''3-Methoxytyramine'''}}|Trace amine={{highlight|[[3-Methoxytyramine]]}}|other=[[3-Methoxytyramine]]}}}}

Revision as of 07:23, 5 January 2020

Biosynthetic pathways for catecholamines and trace amines in the human brain[1][2][3]
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pathway
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In humans, catecholamines and phenethylaminergic trace amines are derived from the amino acid L-phenylalanine.
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{{Catecholamine and trace amine biosynthesis}}

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Template:Reflist talk

  1. ↑ Broadley KJ (March 2010). "The vascular effects of trace amines and amphetamines". Pharmacol. Ther. 125 (3): 363–375. doi:10.1016/j.pharmthera.2009.11.005. PMID 19948186.
  2. ↑ Lindemann L, Hoener MC (May 2005). "A renaissance in trace amines inspired by a novel GPCR family". Trends Pharmacol. Sci. 26 (5): 274–281. doi:10.1016/j.tips.2005.03.007. PMID 15860375.
  3. ↑ Wang X, Li J, Dong G, Yue J (February 2014). "The endogenous substrates of brain CYP2D". Eur. J. Pharmacol. 724: 211–218. doi:10.1016/j.ejphar.2013.12.025. PMID 24374199.
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