About: A-769662   Sponge Permalink

An Entity of Type : dbkwik:resource/rq8Z6H1D5ZQ6xf9ogWx0pw==, within Data Space : 134.155.108.49:8890 associated with source dataset(s)

In the real world, A-769662 was synthesized and characterized by Cool et al. in 2006 at Abbott Laboratories in Illinois, United States of America. Article writer RelentlessRecusant found out about A-769662 through his personal studies in chemical biology.

AttributesValues
rdf:type
rdfs:label
  • A-769662
rdfs:comment
  • In the real world, A-769662 was synthesized and characterized by Cool et al. in 2006 at Abbott Laboratories in Illinois, United States of America. Article writer RelentlessRecusant found out about A-769662 through his personal studies in chemical biology.
  • In 2008, Narkar et al. at the Salk Institute and the Howard Hughes Medical Institute at La Jolla, California would demonstrate that oral administration of 250 mg/kg of a structurally-unrelated and less potent AMPK activator, AICAR, to eight-week-old male C57B/6J mice mediates a 44% increase in endurance without exercise in untrained mice.
dcterms:subject
dbkwik:halo-fanon/...iPageUsesTemplate
dbkwik:halofanon/p...iPageUsesTemplate
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Molweight
  • 360(xsd:double)
Name
  • A-769662
Chemformula
  • C20H12N2O3S
Mechanism
  • AMPK activator
hidepharma
  • yes
Clinuse
  • Exercise mimetic
IUPAC name
  • 4(xsd:integer)
Route
  • Oral
abstract
  • In the real world, A-769662 was synthesized and characterized by Cool et al. in 2006 at Abbott Laboratories in Illinois, United States of America. Article writer RelentlessRecusant found out about A-769662 through his personal studies in chemical biology.
  • In 2008, Narkar et al. at the Salk Institute and the Howard Hughes Medical Institute at La Jolla, California would demonstrate that oral administration of 250 mg/kg of a structurally-unrelated and less potent AMPK activator, AICAR, to eight-week-old male C57B/6J mice mediates a 44% increase in endurance without exercise in untrained mice.
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