Kuiskualinska kiselina
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Nazivi | |||
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IUPAC naziv (2S)-2-amino-3-(3,5-dioxo-1,2,4-oxadiazolidin-2-yl)propanoic acid | |||
Identifikacija | |||
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ECHA InfoCard | 100.164.809 | ||
MeSH | Quisqualic+Acid | ||
PubChem[1][2] C ID |
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Svojstva | |||
C5H7N3O5 | |||
Molarna masa | 189,126 g/mol | ||
Ukoliko nije drugačije napomenuto, podaci se odnose na standardno stanje materijala (na 25 °C [77 °F], 100 kPa). | |||
Reference infokutije | |||
Kuiskualinska kiselina je agonist AMPA receptora i grupe I metabotropskih glutamatnih receptora.[3][4][5] Ona uzrokuje ekscitotoksičnost i koristi se u neurologiji za selektivno uništavanje neurona mozga i kičmene moždine.[6][7][8]
Reference
- ^ 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. PMID 20970519. doi:10.1016/j.drudis.2010.10.003. уреди
- ^ 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.
- ^ Jin, R.; Horning, M.; Mayer, M. L.; Gouaux, E. (2002). „Mechanism of activation and selectivity in a ligand-gated ion channel: Structural and functional studies of GluR2 and quisqualate”. Biochemistry. 41 (52): 15635—43. PMID 12501192. doi:10.1021/bi020583k.
- ^ Kuang, D.; Hampson, D. R. (2006). „Ion dependence of ligand binding to metabotropic glutamate receptors”. Biochemical and Biophysical Research Communications. 345 (1): 1—6. PMID 16674916. doi:10.1016/j.bbrc.2006.04.064.
- ^ Zhang, W.; Robert, A.; Vogensen, S. B.; Howe, J. R. (2006). „The relationship between agonist potency and AMPA receptor kinetics”. Biophysical Journal. 91 (4): 1336—46. PMC 1518651
. PMID 16731549. doi:10.1529/biophysj.106.084426.
- ^ Muir, J. L.; Page, K. J.; Sirinathsinghji, D. J.; Robbins, T. W.; Everitt, B. J. (1993). „Excitotoxic lesions of basal forebrain cholinergic neurons: Effects on learning, memory and attention”. Behavioural Brain Research. 57 (2): 123—31. PMID 7509608. S2CID 3994174. doi:10.1016/0166-4328(93)90128-d.
- ^ Giovannelli L, Casamenti F, Pepeu G. Journal of Neural Transmission. 1998;105(8-9):935-48. „C-fos expression in the rat nucleus basalis upon excitotoxic lesion with quisqualic acid: a study in adult and aged animals.”. PMID 9869327.
- ^ Lee, J. W.; Furmanski, O.; Castellanos, D. A.; Daniels, L. A.; Hama, A. T.; Sagen, J. (2008). „Prolonged nociceptive responses to hind paw formalin injection in rats with a spinal cord injury”. Neuroscience Letters. 439 (2): 212—5. PMC 2680189
. PMID 18524486. doi:10.1016/j.neulet.2008.05.030.
Vidi još
Spoljašnje veze
- Kuiskualinska kiselina
- п
- р
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Grupa I | Agonisti: Neselektivni: ACPD • DHPG • Kuiskualinska kiselina; mGlu1-selektivni: Ro01-6128 • Ro67-4853 • Ro67-7476 • VU-71; mGlu5-selektivni: ADX-47273 • CDPPB • CHPG • DFB • VU-1545 Antagonisti: Neselektivni: MCPG • NPS-2390; mGlu1-selektivni: BAY 36-7620 • CPCCOEt • LY-367,385 • LY-456,236; mGlu5-selektivni: DMeOB • Fenobam • LY-344,545 • MPEP • MTEP • SIB-1757 • SIB-1893 |
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Grupa II | Agonisti: Neselektivni: CBiPES • DCG-IV • Eglumegad • LY-379,268 • LY-404,039 • LY-487,379 • MGS-0028; mGlu2-selektivni: BINA • LY-566,332 Antagonisti: Neselektivni: APICA • EGLU • HYDIA • LY-307,452 • LY-341,495 • MCPG • MGS-0039; mGlu2-selektivni: PCCG-4; mGlu3-selektivni: CECXG; Negativni alosterni modulatori: RO4491533 |
Grupa III | Agonisti: Neselektivni: L-AP4; mGlu4-selektivni: PHCCC • VU-001,171 • VU-0155,041; mGlu7-selektivni: AMN082; mGlu8-selektivni: DCPG Antagonisti: Neselektivni: CPPG • MAP4 • MSOP • MPPG • MTPG • UBP-1112; mGlu7-selektivni: MMPIP |
transporta
EAAT | |
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vGluT |