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α5IA (LS-193,268) is a nootropic drug invented in 2004 by a team working for Merck, Sharp and Dohme, which acts as a subtype-selective inverse agonist at the benzodiazepine binding site on the GABAA receptor. It binds to the α1, α2, α3 and α5 subtypes.

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rdfs:label
  • Α5IA (en)
rdfs:comment
  • α5IA (LS-193,268) is a nootropic drug invented in 2004 by a team working for Merck, Sharp and Dohme, which acts as a subtype-selective inverse agonist at the benzodiazepine binding site on the GABAA receptor. It binds to the α1, α2, α3 and α5 subtypes. (en)
foaf:name
  • α5IA (en)
foaf:depiction
  • http://commons.wikimedia.org/wiki/Special:FilePath/Alpha5IA.svg
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ATC prefix
  • None (en)
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CAS number
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drug name
  • α5IA (en)
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IUPAC name
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PubChem
SMILES
  • CC1=CCC2=NN=C3N2N=COCC5=CNC (en)
StdInChI
StdInChIKey
  • NZMJFRXKGUCYNP-UHFFFAOYSA-N (en)
synonyms
  • LS-193,268 (en)
UNII
has abstract
  • α5IA (LS-193,268) is a nootropic drug invented in 2004 by a team working for Merck, Sharp and Dohme, which acts as a subtype-selective inverse agonist at the benzodiazepine binding site on the GABAA receptor. It binds to the α1, α2, α3 and α5 subtypes. (en)
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page length (characters) of wiki page
CAS number
  • 215874-86-5
FDA UNII code
  • 1M7NI1A92L
PubChem
  • 6918451
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