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Open Access Articles- Top Results for 5-Iodowillardiine

5-Iodowillardiine

5-Iodowillardiine
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IUPAC name
(2S)-2-Amino-3-(5-iodo-2,4-dioxopyrimidin-1-yl)propanoic acid
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140187-25-3 7pxN
ChEMBL ChEMBL121915 7pxY
ChemSpider 394358 7pxY
DrugBank DB02818 7pxY
Jmol-3D images Image
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PubChem Template:Chembox PubChem/format
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C7H8IN3O4
Molar mass Lua error in Module:Math at line 495: attempt to index field 'ParserFunctions' (a nil value). g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references

5-Iodowillardiine is a selective agonist for the kainate receptor, with only limited effects at the AMPA receptor.[1] It is selective for kainate receptors composed of GluR5 subunits.[2][3] It is an excitotoxic neurotoxin in vivo,[4][5] but has proved highly useful for characterising the subtypes and function of the various kainate receptors in the brain and spinal cord.[6][7][8]

References

  1. ^ Patneau, DK; Mayer, ML; Jane, DE; Watkins, JC (1992). "Activation and desensitization of AMPA/kainate receptors by novel derivatives of willardiine". Journal of Neuroscience 12 (2): 595–606. PMID 1371315. 
  2. ^ Swanson, GT; Green, T; Heinemann, SF (1998). "Kainate receptors exhibit differential sensitivities to (S)-5-iodowillardiine". Molecular Pharmacology 53 (5): 942–9. PMID 9584222. 
  3. ^ Cui, C; Mayer, ML (1999). "Heteromeric kainate receptors formed by the coassembly of GluR5, GluR6, and GluR7". Journal of Neuroscience 19 (19): 8281–91. PMID 10493729. 
  4. ^ Moldrich, RX; Cheung, NS; Pascoe, CJ; Beart, PM (1999). "Excitotoxic injury profiles of low-affinity kainate receptor agonists in cortical neuronal cultures". European Journal of Pharmacology 378 (2): R1–3. PMID 10478637. doi:10.1016/S0014-2999(99)00456-2. 
  5. ^ Moldrich, RX; Beart, PM; Pascoe, CJ; Cheung, NS (2000). "Low-affinity kainate receptor agonists induce insult-dependent apoptosis and necrosis in cultured murine cortical neurons". Journal of neuroscience research 59 (6): 788–96. PMID 10700016. doi:10.1002/(SICI)1097-4547(20000315)59:6<788::AID-JNR11>3.0.CO;2-K. 
  6. ^ Mascias, P; Scheede, M; Bloms-Funke, P; Chizh, B (2002). "Modulation of spinal nociception by GluR5 kainate receptor ligands in acute and hyperalgesic states and the role of gabaergic mechanisms". Neuropharmacology 43 (3): 327–39. PMID 12243762. doi:10.1016/S0028-3908(02)00112-0. 
  7. ^ Alt, A; Weiss, B; Ogden, AM; Knauss, JL; Oler, J; Ho, K; Large, TH; Bleakman, D (2004). "Pharmacological characterization of glutamatergic agonists and antagonists at recombinant human homomeric and heteromeric kainate receptors in vitro". Neuropharmacology 46 (6): 793–806. PMID 15033339. doi:10.1016/j.neuropharm.2003.11.026. 
  8. ^ Jane, DE; Lodge, D; Collingridge, GL (2009). "Kainate receptors: pharmacology, function and therapeutic potential". Neuropharmacology 56 (1): 90–113. PMID 18793656. doi:10.1016/j.neuropharm.2008.08.023.