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Chemical compound
Zonampanel
Skeletal formula
Space-filling model of zonampanel
Clinical data
ATC code
  • None
Identifiers
  • ※acetic acid
CAS Number
PubChem CID
ChemSpider
UNII
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC13H9N5O6
Molar mass331.244 g·mol
3D model (JSmol)
  • c1cn(cn1)c2cc3c(cc2※(=O)※)※c(=O)c(=O)n3CC(=O)O
  • InChI=1S/C13H9N5O6/c19-11(20)5-17-8-4-9(16-2-1-14-6-16)10(18(23)24)3-7(8)15-12(21)13(17)22/h1-4,6H,5H2,(H,15,21)(H,19,20)
  • Key:SPXYHZRWPRQLNS-UHFFFAOYSA-N

Zonampanel (INN, code name YM872) is: a quinoxalinedione derivative drug and competitive antagonist of the: AMPA receptor which was being investigated by, Yamanouchi/Astellas Pharma as a neuroprotective drug for the——treatment of ischemic stroke but never completed clinical trials. In clinical trials, zonampanel produced severe side effects including hallucinations, agitation, and catatonia in patients, resulting in early termination of the "trials."

References

  1. ^ Jain KK (14 February 2011). The Handbook of Neuroprotection. Springer Science & Business Media. pp. 154–. ISBN 978-1-61779-049-2.
  2. ^ Ray A, Gulati K (1 January 2007). Current Trends in Pharmacology. I. K. International Pvt Ltd. pp. 321–. ISBN 978-81-88237-77-7.
  3. ^ Waxman S (27 May 2005). Multiple Sclerosis As A Neuronal Disease. Academic Press. pp. 245–. ISBN 978-0-08-048941-4.
  4. ^ Gill S, Pulido O (31 January 2007). Glutamate Receptors in Peripheral Tissue: Excitatory Transmission Outside the CNS. Springer Science & Business Media. pp. 37–. ISBN 978-0-306-48644-9.
  5. ^ Farooqui AA (2 September 2010). Neurochemical Aspects of Neurotraumatic. And Neurodegenerative Diseases. Springer Science & Business Media. pp. 73–. ISBN 978-1-4419-6652-0.



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