Movatterモバイル変換


[0]ホーム

URL:


Jump to content
WikipediaThe Free Encyclopedia
Search

Esproquin

From Wikipedia, the free encyclopedia
Tetrahydroisoquinoline-derivative molecule
Pharmaceutical compound
Esproquin
Clinical data
Other namesEsproquine
Legal status
Legal status
  • Investigational
Identifiers
  • 2-(3-Ethylsulfinylpropyl)-3,4-dihydro-1H-isoquinoline
CAS Number
PubChemCID
UNII
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC14H21NOS
Molar mass251.39 g·mol−1
3D model (JSmol)
  • O=S(CC)CCCN1CC=2C=CC=CC2CC1

Esproquin is anα2-adrenergic receptoragonist derived fromtetrahydroisoquinoline.[1] It has a positive inotropic effect, suggesting potential use in treatment of chronic heart failure.[2]

References

[edit]
  1. ^Gray AP, Shiley RH (July 1973). "Preparation and cardiovascular actions of a group of tetrahydroisoquinoline derivatives".Journal of Medicinal Chemistry.16 (7):859–61.doi:10.1021/jm00265a028.PMID 4146907.
  2. ^Kotelanski B, Grozmann RJ, Cohn JN (1973). "Positive inotropic effect of oral esproquin in normal subjects".Clinical Pharmacology and Therapeutics.14 (3):427–33.doi:10.1002/cpt1973143427.PMID 4698571.S2CID 46266823.
Phenethylamines
Amphetamines
Phentermines
Cathinones
Phenylisobutylamines
(and further-extended)
Catecholamines
(and close relatives)
Cyclized
phenethylamines
Phenylalkylpyrrolidines
2-Benzylpiperidines
(phenidates)
Phenylmorpholines
(phenmetrazines)
Phenyloxazolamines
(aminorexes)
Isoquinolines and
tetrahydroisoquinolines
2-Aminoindanes
2-Aminotetralins
Others / unsorted
Related compounds
Stub icon

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

Retrieved from "https://en.wikipedia.org/w/index.php?title=Esproquin&oldid=1284508355"
Categories:
Hidden categories:

[8]ページ先頭

©2009-2025 Movatter.jp