AMPA: Difference between revisions

AMPA
Names
	IUPAC names 2-amino-3-(5-methyl-3-oxo-1,2-; oxazol-4-yl)propanoic acid
Identifiers
CAS Number	1066-51-9 ;
3D model (JSmol)	Interactive image;
ChEMBL	ChEMBL276815 ;
ChemSpider	1184 ;
DrugBank	DB02057 ;
KEGG	C11033 ;
MeSH	AMPA
PubChem CID	1221;
CompTox Dashboard (EPA)	DTXSID20868301 ;
	InChI InChI=1S/C7H10N2O4/c1-3-4(6(10)9-13-3)2-5(8)7(11)12/h5H,2,8H2,1H3,(H,9,10)(H,11,12) Key: UUDAMDVQRQNNHZ-UHFFFAOYSA-N ; InChI=1/C7H10N2O4/c1-3-4(6(10)9-13-3)2-5(8)7(11)12/h5H,2,8H2,1H3,(H,9,10)(H,11,12) Key: UUDAMDVQRQNNHZ-UHFFFAOYAT;
	SMILES O=C1/C(=C(\ON1)C)CC(N)C(=O)O;
Properties
Chemical formula	C7H10N2O4
Molar mass	186.17 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

Browse history interactively

← Previous edit Next edit →

Content deleted Content added

VisualWikitext

Inline

Revision as of 12:45, 20 October 2011

AMPA (2-amino-3-(5-methyl-3-oxo-1,2- oxazol-4-yl)propanoic acid) is a compound that is a specific agonist for the AMPA receptor, where it mimics the effects of the neurotransmitter glutamate.^[1]

There are two types of [Ionotropic glutamate receptors that are ligand gated ion channels whose agonists include AMPA, Kainate and NMDA. In the synapse, these two classes of receptors serve very different purposes. AMPA can be used experimentally to distinguish the activity of one receptor from the other in order to understand their differing functions.^[2] AMPA generates fast excitatory postsynaptic potentials (EPSP).^[1] AMPA activates AMPA receptors that are non-selective cationic channels allowing the passage of Na+ and K+ and therefore have an equilibrium potential near 0 mV.

References

^ ^a ^b Purves, Dale, George J. Augustine, David Fitzpatrick, William C. Hall, Anthony-Samuel LaMantia, James O. McNamara, and Leonard E. White (2008). Neuroscience. 4th ed. Sinauer Associates. pp. 128–33. ISBN 978-0-87893-697-7.{{cite book}}: CS1 maint: multiple names: authors list (link)
^ Dinh, L (2009). "Norepinephrine homogeneously inhibits alpha-amino-3-hydroxyl-5-methyl-4-isoxazole-propionate- (AMPAR-) mediated currents in all layers of the temporal cortex of the rat". Neurochem Res. 34 (11): 1896–906. doi:10.1007/s11064-009-9966-z. PMID 19357950. {{cite journal}}: Unknown parameter |coauthors= ignored (|author= suggested) (help)

[Purves2008-1] Purves, Dale, George J. Augustine, David Fitzpatrick, William C. Hall, Anthony-Samuel LaMantia, James O. McNamara, and Leonard E. White (2008). Neuroscience. 4th ed. Sinauer Associates. pp. 128–33. ISBN 978-0-87893-697-7.{{cite book}}: CS1 maint: multiple names: authors list (link)

[Dinh2009-2] Dinh, L (2009). "Norepinephrine homogeneously inhibits alpha-amino-3-hydroxyl-5-methyl-4-isoxazole-propionate- (AMPAR-) mediated currents in all layers of the temporal cortex of the rat". Neurochem Res. 34 (11): 1896–906. doi:10.1007/s11064-009-9966-z. PMID 19357950. {{cite journal}}: Unknown parameter |coauthors= ignored (|author= suggested) (help)

[1]

[2]

@@ Line 10: / Line 10: @@
 |   InChIKey = UUDAMDVQRQNNHZ-UHFFFAOYAT
 | CASNo_Ref = {{cascite}}
-| CASNo = <!-- blanked - oldvalue: 1066-51-9 -->
+| CASNo = 1066-51-9
 |   PubChem = 1221
 | ChEMBL_Ref = {{ebicite|changed|EBI}}
-| ChEMBL = 13378
+| ChEMBL = 276815
 |   DrugBank_Ref = {{drugbankcite|changed|drugbank}}
 | DrugBank = DB02057