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Idalopirdine
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Idalopirdine

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Idalopirdine
Lu-AE58054.svg
Clinical data
Other names Lu-AE-58054
ATC code
  • None
Identifiers
  • 2-(6-Fluoro-1H-indol-3-yl)-N-(3-(2,2,3,3-tetrafluoropropoxy)benzyl)ethanamine
CAS Number
PubChem CID
ChemSpider
UNII
KEGG
ChEMBL
ECHA InfoCard 100.245.270
Chemical and physical data
Formula C20H19F5N2O
Molar mass 398.377 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) (code names Lu AE58054,) is a potent and selective 5-HT6 receptor antagonist under development by Lundbeck as an augmentation therapy for the treatment of cognitive deficits associated with Alzheimer's disease and schizophrenia. As of October 2013 it is in phase III clinical trials.

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

See also

External links


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