Icilin: Difference between revisions

Icilin
Names
	IUPAC name 1-(2-hydroxyphenyl)-4-(3-nitrophenyl)-3,6-dihydropyrimidin-2-one
	Other names AG-3-5
Identifiers
CAS Number	36945-98-9 ;
3D model (JSmol)	Interactive image;
ChemSpider	142218 ;
ECHA InfoCard	100.164.593
IUPHAR/BPS	2429;
PubChem CID	161930;
CompTox Dashboard (EPA)	DTXSID70190442 ;
	InChI InChI=1S/C16H13N3O4/c20-15-7-2-1-6-14(15)18-9-8-13(17-16(18)21)11-4-3-5-12(10-11)19(22)23/h1-8,10,20H,9H2,(H,17,21) Key: RCEFMOGVOYEGJN-UHFFFAOYSA-N ; InChI=1/C16H13N3O4/c20-15-7-2-1-6-14(15)18-9-8-13(17-16(18)21)11-4-3-5-12(10-11)19(22)23/h1-8,10,20H,9H2,(H,17,21) Key: RCEFMOGVOYEGJN-UHFFFAOYAQ;
	SMILES O=C3N(c1c(O)cccc1)C/C=C(/c2cccc([N+]([O-])=O)c2)N3;
Properties
Chemical formula	C16H13N3O4
Molar mass	311.29 g/mol
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). verify (what is ?) Infobox references

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Revision as of 15:15, 14 December 2012

Icilin is a synthetic super-agonist of the transient receptor potential M8 (TRPM8) ion channel. Although structurally not related with menthol it produces an extreme sensation of cold both in humans and animals. It is almost 200 times more potent than menthol and 2.5 times more efficacious.^[1] Despite their similar effects icilin activates the TRPM8 receptor in a different way.^[2] Icilin is effective in an experimental model of itch.^[3] It is now used as a research tool for the study of TRP channels.

References

^ Wei ET, Seid DA (1983). "AG-3-5: a chemical producing sensations of cold". J. Pharm. Pharmacol. 35 (2): 110–2. PMID 6131976.
^ Andersson DA, Chase HW, Bevan S (2004). "TRPM8 activation by menthol, icilin, and cold is differentially modulated by intracellular pH". J. Neurosci. 24 (23): 5364–9. doi:10.1523/JNEUROSCI.0890-04.2004. PMID 15190109.{{cite journal}}: CS1 maint: multiple names: authors list (link)
^ Biró, T; Ko, MC; Bromm, B; Wei, ET; Bigliardi, P; Siebenhaar, F; Hashizume, H; Misery, L; Bergasa, NV (2005). "How best to fight that nasty itch - from new insights into the neuroimmunological, neuroendocrine, and neurophysiological bases of pruritus to novel therapeutic approaches". Experimental Dermatology. 14 (3): 225–40. doi:10.1111/j.0906-6705.2005.0321a.x. PMID 15740597.

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[pmid6131976-1] Wei ET, Seid DA (1983). "AG-3-5: a chemical producing sensations of cold". J. Pharm. Pharmacol. 35 (2): 110–2. PMID 6131976.

[pmid15190109-2] Andersson DA, Chase HW, Bevan S (2004). "TRPM8 activation by menthol, icilin, and cold is differentially modulated by intracellular pH". J. Neurosci. 24 (23): 5364–9. doi:10.1523/JNEUROSCI.0890-04.2004. PMID 15190109.{{cite journal}}: CS1 maint: multiple names: authors list (link)

[pmid15740597-3] Biró, T; Ko, MC; Bromm, B; Wei, ET; Bigliardi, P; Siebenhaar, F; Hashizume, H; Misery, L; Bergasa, NV (2005). "How best to fight that nasty itch - from new insights into the neuroimmunological, neuroendocrine, and neurophysiological bases of pruritus to novel therapeutic approaches". Experimental Dermatology. 14 (3): 225–40. doi:10.1111/j.0906-6705.2005.0321a.x. PMID 15740597.

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 == External links ==
 * [http://www.caymanchem.com/app/template/Product.vm/catalog/10137/a/z Product sheet of Icilin from Cayman Chemical]
+*[http://www.tocris.com/dispprod.php?ItemId=38283 Product page for Icilin from Tocris Bioscience]
 [[Category:Phenols]]