Adipiplon

Not to be confused with adipiodone.

Adipiplon

Systematic (IUPAC) name
7-[(2-(3-fluoropyridin-2-yl)-1H-imidazol-1-yl)methyl]-2-methyl-8-propyl-[1,2,4]triazolo[1,5-c]pyrimidine
Clinical data
Legal status	Uncontrolled
Routes of administration	Oral
Identifiers
CAS Number	840486-93-3 N
ATC code	none
ChemSpider	9373993 Y
UNII	OPL214POJ1 Y
KEGG	D08840 Y
ChEMBL	CHEMBL2103791 N
Chemical data
Formula	C18H18FN7
Molecular mass	351.38 g/mol
SMILES n4c(C)nc1n4cnc(c1CCC)Cn2ccnc2-c3ncccc3F
InChI InChI=1S/C18H18FN7/c1-3-5-13-15(22-11-26-17(13)23-12(2)24-26)10-25-9-8-21-18(25)16-14(19)6-4-7-20-16/h4,6-9,11H,3,5,10H2,1-2H3 Y Key:UAMAIHOEGLEXSV-UHFFFAOYSA-N Y
NY (what is this?)  (verify)

Adipiplon (NG2-73) is an anxiolytic drug developed by Neurogen Corporation. It has similar effects to benzodiazepine drugs, but is structurally distinct and so is classed as a nonbenzodiazepine anxiolytic.

Adipiplon is a subtype-selective GABA_A receptor partial agonist, which binds preferentially to the α₃ subtype. This is significant as while several previous nonbenzodiazepine drugs have been developed that are selective for α_2/3 over the other subtypes, adipiplon is one of the first drugs selected for clinical development which is able to discriminate between α₂ and α₃, as well as showing little affinity for the α₁ or α₅ subtypes - alpidem is selective for α₃ over α₂, but still has moderate affinity for α₁, whereas adipiplon is highly α₃-selective with little affinity for either α₁, α₂ or α₅.

Adipiplon is being researched as a potential medication for the treatment of anxiety and insomnia, and is currently (as of 2008) in Phase IIb trials.

See also

• Nonbenzodiazepine