L-AP4
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| (IUPAC) ime | |||
|---|---|---|---|
| (2S)-2-amino-4-fosfonobutanoinska kiselina | |||
| Klinički podaci | |||
| Identifikatori | |||
| CAS broj | 23052-81-5 | ||
| ATC kod | nije dodeljen | ||
| PubChem[1][2] | 179394 | ||
| Hemijski podaci | |||
| Formula | C4H10NO5P | ||
| Mol. masa | 183,099 g/mol | ||
| SMILES | eMolekuli & PubHem | ||
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| Farmakoinformacioni podaci | |||
| Trudnoća | ? | ||
| Pravni status | |||
L-AP4 je lek koji se koristi u naučnim istraživanjima. On deluje kao agonist koji je selektivan za grupu III metabotropnih glutamatnih receptora (mGluR4/6/7/8). On je bio privi ligand za koji je utvrđeno da deluje kao selektivni agonist za ovu grupu mGlu receptora.[3] On se koristi u izučavanju ove receptorske familije i njihovih funkcija.[4][5][6][7]
Reference[uredi | uredi kod]
- ↑ Li Q, Cheng T, Wang Y, Bryant SH (2010). „PubChem as a public resource for drug discovery.”. Drug Discov Today 15 (23-24): 1052-7. DOI:10.1016/j.drudis.2010.10.003. PMID 20970519.
- ↑ Evan E. Bolton, Yanli Wang, Paul A. Thiessen, Stephen H. Bryant (2008). „Chapter 12 PubChem: Integrated Platform of Small Molecules and Biological Activities”. Annual Reports in Computational Chemistry 4: 217-241. DOI:10.1016/S1574-1400(08)00012-1.
- ↑ Thomsen C (1997). „The L-AP4 receptor”. General pharmacology 29 (2): 151–8. PMID 9251893.
- ↑ 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.
- ↑ 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.
- ↑ 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.
- ↑ 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.
