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A-366,833

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Chemical compound
Pharmaceutical compound
A-366,833
Identifiers
  • 5-[(1R,5S)-3,6-Diazabicyclo[3.2.0]hept-6-yl]pyridine-3-carbonitrile
CAS Number
PubChemCID
ChemSpider
UNII
ChEMBL
Chemical and physical data
FormulaC11H12N4
Molar mass200.245 g·mol−1
3D model (JSmol)
Melting point101.4–102.9 °C (214.5–217.2 °F)[1]
  • N#CC1=CN=CC(N2[C@]3([H])CNC[C@]3([H])C2)=C1
  • InChI=1S/C11H12N4/c12-2-8-1-10(5-13-3-8)15-7-9-4-14-6-11(9)15/h1,3,5,9,11,14H,4,6-7H2/t9-,11-/m1/s1 ☒N
  • Key:GPXAWLDGWSBLKM-MWLCHTKSSA-N ☒N
 ☒NcheckY (what is this?)  (verify)

A-366,833 is a drug developed byAbbott, which acts as an agonist at neuralnicotinic acetylcholine receptors selective for theα4β2 subtype, and has been researched for use as ananalgesic, although it has not passedclinical trials.[2] Its structure has a nicotinonitrile (3-cyanopyridine) core bound through C5 to the N6 of (1R,5S)-3,6-diazabicyclo[3.2.0]heptane.[3]

References

[edit]
  1. ^Ji J, Schrimpf MR, Sippy KB, Bunnelle WH, Li T, Anderson DJ, et al. (November 2007). "Synthesis and structure-activity relationship studies of 3,6-diazabicyclo[3.2.0]heptanes as novel alpha4beta2 nicotinic acetylcholine receptor selective agonists".Journal of Medicinal Chemistry.50 (22):5493–508.doi:10.1021/jm070755h.PMID 17929796.
  2. ^Romanelli MN, Gratteri P, Guandalini L, Martini E, Bonaccini C, Gualtieri F (June 2007). "Central nicotinic receptors: structure, function, ligands, and therapeutic potential".ChemMedChem.2 (6):746–67.doi:10.1002/cmdc.200600207.PMID 17295372.S2CID 34763474.
  3. ^Ji J, Bunnelle WH, Anderson DJ, Faltynek C, Dyhring T, Ahring PK, et al. (October 2007). "A-366833: a novel nicotinonitrile-substituted 3,6-diazabicyclo[3.2.0]-heptane alpha4beta2 nicotinic acetylcholine receptor selective agonist: Synthesis, analgesic efficacy and tolerability profile in animal models".Biochemical Pharmacology.74 (8):1253–62.doi:10.1016/j.bcp.2007.08.010.PMID 17854775.
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