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ELB-139

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
ELB-139
Identifiers
  • 1-(4-Chlorophenyl)-4-piperidin-1-yl-1,5-dihydro-imidazol-2-one
CAS Number
PubChemCID
ChemSpider
UNII
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC14H16ClN3O
Molar mass277.75 g·mol−1
3D model (JSmol)
  • Clc3ccc(cc3)N1CC(=NC1=O)N2CCCCC2
  • InChI=1S/C14H16ClN3O/c15-11-4-6-12(7-5-11)18-10-13(16-14(18)19)17-8-2-1-3-9-17/h4-7H,1-3,8-10H2
  • Key:YGXIELIREXEJQN-UHFFFAOYSA-N
  (verify)

ELB-139 (LS-191,811) is ananxiolytic drug with a novel chemical structure, which is used in scientific research. It has similar effects tobenzodiazepine drugs, but is structurally distinct and so is classed as anonbenzodiazepine anxiolytic.[1][2]

ELB-139 is a subtype-selectivepartial agonist atGABAA receptors, with highestaffinity for the α3 subtype, but highestefficacy at α1 and α2.[3] It has primarilyanxiolytic andanticonvulsant effects, but produces littlesedative effects orataxia,[4] and has also been demonstrated in rats to increaseserotonin levels in thestriatum andprefrontal cortex, without affectingdopamine levels.[5] It has been proposed as a possible candidate for a novel non-sedating anxiolytic or anticonvulsant drug for use in humans[6] The sponsor elbion AG registered a clinical trial inClinicalTrials.govfor the treatment of anxiety associated with panic disorder but the results have not been reported.[7] It was developed by Arzneimittelwerk Dresden in the 1990s.[8]

References

[edit]
  1. ^Langen B, Egerland U, Bernöster K, Dost R, Unverferth K, Rundfeldt C (August 2005). "Characterization in rats of the anxiolytic potential of ELB139 [1-(4-chlorophenyl)-4-piperidin-1-yl-1,5-dihydro-imidazol-2-on], a new agonist at the benzodiazepine binding site of the GABAA receptor".The Journal of Pharmacology and Experimental Therapeutics.314 (2):717–24.doi:10.1124/jpet.105.084681.PMID 15860576.S2CID 21967108.
  2. ^Atack JR (May 2005). "The benzodiazepine binding site of GABA(A) receptors as a target for the development of novel anxiolytics".Expert Opinion on Investigational Drugs.14 (5):601–18.doi:10.1517/13543784.14.5.601.PMID 15926867.S2CID 22793644.
  3. ^Rabe H, Kronbach C, Rundfeldt C, Lüddens H (March 2007). "The novel anxiolytic ELB139 displays selectivity to recombinant GABA(A) receptors different from diazepam".Neuropharmacology.52 (3):796–801.doi:10.1016/j.neuropharm.2006.09.013.PMID 17087982.S2CID 21598180.
  4. ^Grunwald C, Rundfeldt C, Lankau HJ, Arnold T, Höfgen N, Dost R, et al. (March 2006). "Synthesis, pharmacology, and structure-activity relationships of novel imidazolones and pyrrolones as modulators of GABAA receptors".Journal of Medicinal Chemistry.49 (6):1855–66.doi:10.1021/jm0509400.PMID 16539371.
  5. ^Langen B, Rundfeldt C (January 2007). "ELB139 an agonist at the benzodiazepine binding site increases 5-HT in the striatum and prefrontal cortex of rats: a microdialysis study".Pharmacology, Biochemistry, and Behavior.86 (1):79–85.doi:10.1016/j.pbb.2006.12.010.PMID 17257662.S2CID 22862432.
  6. ^Rogawski MA (June 2006)."Diverse mechanisms of antiepileptic drugs in the development pipeline".Epilepsy Research.69 (3):273–94.doi:10.1016/j.eplepsyres.2006.02.004.PMC 1562526.PMID 16621450.
  7. ^Whiting PJ (February 2006). "GABA-A receptors: a viable target for novel anxiolytics?".Current Opinion in Pharmacology.6 (1):24–9.doi:10.1016/j.coph.2005.08.005.PMID 16359919.
  8. ^US 5869481, "Anticonvulsive 1-ar(alk)ylimidazolin-2-ones and process for making" 
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