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PEPA
Clinical data
Other namesPEPA
Legal status
Legal status
Identifiers
  • 2-[2,6-difluoro-4-({2-[(phenylsulfonyl)amino]ethyl}thio)phenoxy]acetamide
CAS Number
PubChem CID
ChemSpider
UNII
CompTox Dashboard ( EPA)
Chemical and physical data
FormulaC16H16F2N2O4S2
Molar mass402.43 g·mol−1
3D model ( JSmol)
  • C1=CC=C(C=C1)S(=O)(=O)NCCSC2=CC(=C(C(=C2)F)OCC(=O)N)F
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PEPA is a sulfonamide AMPA receptor positive allosteric modulator, [1] [2] which is up to 100 times more potent than aniracetam in vitro. [3] It produces memory-enhancing effects in rats when administered intravenously. [4]

See also

References

  1. ^ Sekiguchi M, Takeo J, Harada T, Morimoto T, Kudo Y, Yamashita S, et al. (April 1998). "Pharmacological detection of AMPA receptor heterogeneity by use of two allosteric potentiators in rat hippocampal cultures". British Journal of Pharmacology. 123 (7): 1294–303. doi: 10.1038/sj.bjp.0701707. PMC  1565288. PMID  9579722.
  2. ^ Sekiguchi M, Nishikawa K, Aoki S, Wada K (August 2002). "A desensitization-selective potentiator of AMPA-type glutamate receptors". British Journal of Pharmacology. 136 (7): 1033–41. doi: 10.1038/sj.bjp.0704804. PMC  1573432. PMID  12145103.
  3. ^ Sekiguchi M, Fleck MW, Mayer ML, Takeo J, Chiba Y, Yamashita S, Wada K (August 1997). "A novel allosteric potentiator of AMPA receptors: 4--2-(phenylsulfonylamino)ethylthio--2,6-difluoro-phenoxyaceta mide". The Journal of Neuroscience. 17 (15): 5760–71. doi: 10.1523/JNEUROSCI.17-15-05760.1997. PMC  6573208. PMID  9221774.
  4. ^ Sekiguchi M, Yamada K, Jin J, Hachitanda M, Murata Y, Namura S, et al. (September 2001). "The AMPA receptor allosteric potentiator PEPA ameliorates post-ischemic memory impairment". NeuroReport. 12 (13): 2947–50. doi: 10.1097/00001756-200109170-00038. PMID  11588608. S2CID  42785890.