Amibegron

Chemical compound
  • none
Legal statusLegal status
  • Development terminated
Identifiers
  • Ethyl ([(7S)-7-([(2R)-2-(3-chlorophenyl)-2-hydroxyethyl]amino)-5,6,7,8-tetrahydronaphthalen-2-yl]oxy)acetate
CAS Number
  • 121524-08-1 checkY
  • HCl: 121524-09-2 checkY
PubChem CID
  • 3035442
IUPHAR/BPS
  • 568
ChemSpider
  • 108738 checkY
UNII
  • PDQ3ME68U3
  • HCl: N910CJ679E checkY
KEGG
  • D08851 checkY
ChEMBL
  • ChEMBL545437 checkY
CompTox Dashboard (EPA)
  • DTXSID6047361 Edit this at Wikidata
Chemical and physical dataFormulaC22H26ClNO4Molar mass403.90 g·mol−13D model (JSmol)
  • Interactive image
  • CCOC(=O)COc3ccc1CCC(Cc1c3)NCC(O)c2cc(Cl)ccc2
InChI
  • InChI=1S/C22H26ClNO4.ClH/c1-2-27-22(26)14-28-20-9-7-15-6-8-19(11-17(15)12-20)24-13-21(25)16-4-3-5-18(23)10-16;/h3-5,7,9-10,12,19,21,24-25H,2,6,8,11,13-14H2,1H3;1H/t19-,21-;/m0./s1 checkY
  • Key:NQIZCDQCNYCVAS-RQBPZYBGSA-N checkY
  (verify)

Amibegron (SR-58,611A) was a drug developed by Sanofi-Aventis (now Sanofi) which acts as a selective agonist for the β3 adrenergic receptor. It is the first orally active β3 agonist developed that is capable of entering the central nervous system, and has antidepressant and anxiolytic effects.[1][2]

On July 31, 2008, Sanofi-Aventis announced that it has decided to discontinue development of amibegron.[3]

References

  1. ^ Stemmelin J, Cohen C, Terranova JP, Lopez-Grancha M, Pichat P, Bergis O, et al. (February 2008). "Stimulation of the beta3-Adrenoceptor as a novel treatment strategy for anxiety and depressive disorders". Neuropsychopharmacology. 33 (3): 574–87. doi:10.1038/sj.npp.1301424. PMID 17460614.
  2. ^ Overstreet DH, Stemmelin J, Griebel G (June 2008). "Confirmation of antidepressant potential of the selective beta3 adrenoceptor agonist amibegron in an animal model of depression". Pharmacology, Biochemistry, and Behavior. 89 (4): 623–6. doi:10.1016/j.pbb.2008.02.020. PMID 18358519. S2CID 35026036.
  3. ^ Second quarter 2008 results. July 31, 2008, retrieved March 9, 2009.
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