Jump to content

Lanicemine

From Wikipedia, the free encyclopedia
Lanicemine
Clinical data
ATC code
  • none
Legal status
Legal status
  • Development terminated
Identifiers
  • (1S)-1-Phenyl-2-pyridin-2-ylethanamine
CAS Number
PubChemCID
IUPHAR/BPS
ChemSpider
UNII
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC13H14N2
Molar mass198.269g·mol−1
3D model (JSmol)
  • N[C@H](C1=CC=CC=C1)CC2=NC=CC=C2
  • InChI=1S/C13H14N2/c14-13(11-6-2-1-3-7-11)10-12-8-4-5-9-15-12/h1-9,13H,10,14H2/t13-/m0/s1
  • Key:FWUQWDCOOWEXRY-ZDUSSCGKSA-N

Lanicemine(AZD6765) is a low-trappingNMDA receptor antagonistthat was underdevelopmentbyAstraZenecafor the management of severe andtreatment-resistant depression.[1][2]Lanicemine differs fromketaminein that it is alow-trappingNMDA receptorantagonist, showing similar rapid-acting antidepressant effects to ketamine in clinical trials but with little or no psychotomimetic side effects.[3]However, lanicemine did not meet study endpoints, and its development was terminated by AstraZeneca in 2013.[4]

See also[edit]

References[edit]

  1. ^"Lanicemine".AdisInsight.Retrieved18 June2017.
  2. ^Machado-Vieira R, Henter ID, Zarate CA (May 2017)."New targets for rapid antidepressant action".Progress in Neurobiology.152:21–37.doi:10.1016/j.pneurobio.2015.12.001.PMC4919246.PMID26724279.
  3. ^Zarate CA, Mathews D, Ibrahim L, Chaves JF, Marquardt C, Ukoh I, et al. (August 2013)."A randomized trial of a low-trapping nonselective N-methyl-D-aspartate channel blocker in major depression".Biological Psychiatry.74(4): 257–64.doi:10.1016/j.biopsych.2012.10.019.PMC3594049.PMID23206319.
  4. ^Flowers S."Return to growth: AstraZeneca's CEO Pascal Soriot says 2013 was year of" momentum "for the company".Retrieved6 February2014.