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L-AP4: Difference between revisions

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Updating {{drugbox}} (changes to watched fields - added verified revid - updated 'ChemSpiderID_Ref', 'DrugBank_Ref', 'UNII_Ref', 'ChEMBL_Ref', 'ChEBI_Ref', 'KEGG_Ref', 'StdInChI_Ref', 'StdInChIKey_Ref', 'ChEBI_Ref') per [[WP:CHEMVALID|Chem/Drugbox va
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{{Drugbox
| Watchedfields = changed
| verifiedrevid = 402322108
| verifiedrevid = 438864433
| IUPAC_name = (2S)-2-amino-4-phosphonobutanoic acid
| IUPAC_name = (2S)-2-amino-4-phosphonobutanoic acid
| image = L-AP4_structure.png
| image = L-AP4_structure.png
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| PubChem = 179394
| PubChem = 179394
| IUPHAR_ligand = 1412
| IUPHAR_ligand = 1412
| DrugBank_Ref = {{drugbankcite|correct|drugbank}}
| DrugBank =
| DrugBank =



Revision as of 22:51, 18 September 2011

L-AP4
Identifiers
  • (2S)-2-amino-4-phosphonobutanoic acid
CAS Number
PubChem CID
IUPHAR/BPS
CompTox Dashboard (EPA)
ECHA InfoCard100.164.384 Edit this at Wikidata
Chemical and physical data
FormulaC4H10NO5P
Molar mass183.099 g/mol g·mol−1
3D model (JSmol)
  • OC(=O)C(N)CCP(O)(O)=O
  (verify)

L-AP4 is a drug used in scientific research, which acts as a group-selective agonist for the group III metabotropic glutamate receptors (mGluR4/6/7/8). It was the first ligand found to act as an agonist selective for this group of mGlu receptors,[1] but does not show selectivity between the different mGluR Group III subtypes. It is widely used in the study of this receptor family and their various functions.[2][3][4][5]

References

  1. ^ Thomsen, C (1997). "The L-AP4 receptor". General pharmacology. 29 (2): 151–8. PMID 9251893. {{cite journal}}: Cite has empty unknown parameter: |author-name-separator= (help); Unknown parameter |author-separator= ignored (help)
  2. ^ Lopez, S; Turle-Lorenzo, N; Acher, F; De Leonibus, E; Mele, A; Amalric, M (2007). "Targeting group III metabotropic glutamate receptors produces complex behavioral effects in rodent models of Parkinson's disease". Journal of Neuroscience. 27 (25): 6701–11. doi:10.1523/JNEUROSCI.0299-07.2007. PMID 17581957. {{cite journal}}: Cite has empty unknown parameter: |author-name-separator= (help); Unknown parameter |author-separator= ignored (help)
  3. ^ MacInnes, N; Duty, S (2008). "Group III metabotropic glutamate receptors act as hetero-receptors modulating evoked GABA release in the globus pallidus in vivo". European journal of pharmacology. 580 (1–2): 95–9. doi:10.1016/j.ejphar.2007.10.030. PMID 18035348. {{cite journal}}: Cite has empty unknown parameter: |author-name-separator= (help); Unknown parameter |author-separator= ignored (help)
  4. ^ Zhang, HM; Chen, SR; Pan, HL (2009). "Effects of activation of group III metabotropic glutamate receptors on spinal synaptic transmission in a rat model of neuropathic pain". Neuroscience. 158 (2): 875–84. doi:10.1016/j.neuroscience.2008.10.042. PMC 2649787. PMID 19017536. {{cite journal}}: Cite has empty unknown parameter: |author-name-separator= (help); Unknown parameter |author-separator= ignored (help)
  5. ^ MacIejak, P; Szyndler, J; Turzyńska, D; Sobolewska, A; Taracha, E; Skórzewska, A; Lehner, M; Bidziński, A; Hamed, A (2009). "The effects of group III mGluR ligands on pentylenetetrazol-induced kindling of seizures and hippocampal amino acids concentration". Brain research. 1282: 20–7. doi:10.1016/j.brainres.2009.05.049. PMID 19481536. {{cite journal}}: Cite has empty unknown parameter: |author-name-separator= (help); Unknown parameter |author-separator= ignored (help)