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Idalopirdine

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
Idalopirdine
Clinical data
Other namesLu-AE-58054
ATC code
  • None
Identifiers
  • 2-(6-Fluoro-1H-indol-3-yl)-N-(3-(2,2,3,3-tetrafluoropropoxy)benzyl)ethanamine
CAS Number
PubChemCID
ChemSpider
UNII
KEGG
ChEMBL
CompTox Dashboard(EPA)
ECHA InfoCard100.245.270Edit this at Wikidata
Chemical and physical data
FormulaC20H19F5N2O
Molar mass398.377 g·mol−1
3D model (JSmol)
  • FC(F)C(F)(F)COc1cccc(c1)CNCCc3c[nH]c2cc(F)ccc23
  • InChI=1S/C20H19F5N2O/c21-15-4-5-17-14(11-27-18(17)9-15)6-7-26-10-13-2-1-3-16(8-13)28-12-20(24,25)19(22)23/h1-5,8-9,11,19,26-27H,6-7,10,12H2 ☒N
  • Key:YBAWYTYNMZWMMJ-UHFFFAOYSA-N ☒N
 ☒NcheckY (what is this?)  (verify)

Idalopirdine (INN; development codeLu AE58054) is apotent andselective5-HT6 receptorantagonist under development byLundbeck as anaugmentation therapy for the treatment ofcognitive deficits associated withAlzheimer's disease andschizophrenia.[1][2] As of October 2013 it is inphase III clinical trials.[2]

A phase III trial of two different daily doses of Lu AE58054 on top of 10 mg ofdonepezil for mild-to-moderate Alzheimer's failed to meet itsprimary endpoint with either dose.[3] Two further phase III trials failed too, the company confirmed in early 2017.[3]

See also

[edit]

References

[edit]
  1. ^"U.S. Development Programs".Lundbeck.
  2. ^ab"Search of: Lu AE58054 - List Results".ClinicalTrials.gov. National Library of Medicine, U.S. Department of Health and Human Services.
  3. ^abTaylor NP (23 September 2016)."PhIII Alzheimer's flop takes chunk out of Lundbeck, hits Axovant with aftershocks".

External links

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Psychoanaleptics: Anti-dementia agents (ATC codeN06D and others)
AChE inhibitor medications
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ExperimentalBACE inhibitors
5-HT1
5-HT1A
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5-HT1D
5-HT1E
5-HT1F
5-HT2
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5-HT2C
5-HT37
5-HT3
5-HT4
5-HT5A
5-HT6
5-HT7
Tryptamines
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andesters/ethers
5-Hydroxy- and
5-methoxytryptamines
N-Acetyltryptamines
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