Movatterモバイル変換


[0]ホーム

URL:


Jump to content
WikipediaThe Free Encyclopedia
Search

LY-456220

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
LY-456220
Identifiers
  • (S)-1-(2-(4-(6-fluoro-1H-indol-3-yl)-3,6-dihydropyridin-1(2H)-yl)ethyl)isochromane-6-carboxamide
CAS Number
PubChemCID
Chemical and physical data
FormulaC25H26FN3O2
Molar mass419.500 g·mol−1
3D model (JSmol)
  • C1CN(CC=C1C2=CNC3=C2C=CC(=C3)F)CCC4C5=C(CCO4)C=C(C=C5)C(=O)N
  • InChI=1S/C25H26FN3O2/c26-19-2-4-21-22(15-28-23(21)14-19)16-5-9-29(10-6-16)11-7-24-20-3-1-18(25(27)30)13-17(20)8-12-31-24/h1-5,13-15,24,28H,6-12H2,(H2,27,30)/t24-/m0/s1
  • Key:AYGLZYIWAZBQDC-DEOSSOPVSA-N

LY-456220 is a potent and selectiveserotonin 5-HT1D receptorantagonist which has been used in research to study the function of presynaptic 5-HT1Dautoreceptors. LY-456220 lacks significant affinity for the5-HT1B,α1 adrenergic, anddopamine D2 receptors.[1][2]It is anenantiomer ofLY-456219.

References

[edit]
  1. ^Pullar IA, Boot JR, Broadmore RJ, Eyre TA, Cooper J, Sanger GJ, et al. (June 2004). "The role of the 5-HT1D receptor as a presynaptic autoreceptor in the guinea pig".European Journal of Pharmacology.493 (1–3):85–93.doi:10.1016/j.ejphar.2004.04.029.PMID 15189767.
  2. ^Timms GH, Boot JR, Broadmore RJ, Carney SL, Cooper J, Findlay JD, et al. (May 2004). "SAR development of a selective 5-HT1D antagonist/serotonin reuptake inhibitor lead using rapid parallel synthesis".Bioorganic & Medicinal Chemistry Letters.14 (10):2469–72.doi:10.1016/j.bmcl.2004.03.003.PMID 15109634.
5-HT1
5-HT1A
5-HT1B
5-HT1D
5-HT1E
5-HT1F
5-HT2
5-HT2A
5-HT2B
5-HT2C
5-HT37
5-HT3
5-HT4
5-HT5A
5-HT6
5-HT7
Stub icon

Thisdrug article relating to thenervous system is astub. You can help Wikipedia byexpanding it.

Retrieved from "https://en.wikipedia.org/w/index.php?title=LY-456220&oldid=1252157563"
Categories:
Hidden categories:

[8]ページ先頭

©2009-2025 Movatter.jp