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Soquinolol

From Wikipedia, the free encyclopedia
Soquinolol
Names
IUPAC name
5-[3-(tert-Butylamino)-2-hydroxypropoxy]-3,4-dihydro-1H-isoquinoline-2-carbaldehyde
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard100.057.113Edit this at Wikidata
UNII
  • InChI=1S/C17H26N2O3/c1-17(2,3)18-9-14(21)11-22-16-6-4-5-13-10-19(12-20)8-7-15(13)16/h4-6,12,14,18,21H,7-11H2,1-3H3
    Key: GMJHUSJLZXFFQJ-UHFFFAOYSA-N
  • InChI=1/C17H26N2O3/c1-17(2,3)18-9-14(21)11-22-16-6-4-5-13-10-19(12-20)8-7-15(13)16/h4-6,12,14,18,21H,7-11H2,1-3H3
    Key: GMJHUSJLZXFFQJ-UHFFFAOYAM
  • CC(C)(C)NCC(COC1=CC=CC2=C1CCN(C2)C=O)O
  • CC(C)(C)NCC(COc1cccc2c1CCN(C2)C=O)O
Properties
C17H26N2O3
Molar mass306.406 g·mol−1
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
Chemical compound

Soquinolol is abeta adrenergic receptor antagonist.[1]

References

[edit]
  1. ^Gries, J; Unger, L; Einig, H; Friedrich, L; Hofmann, HP; Kreiskott, H; Lehmann, HD; Von Philipsborn, G; Wuppermann, D; Zimmermann, F (1988). "Pharmacological characterization of the new highly potent beta-adrenergic receptor blocker soquinolol".Arzneimittel-Forschung.38 (9):1271–9.PMID 2906243.


α1
Agonists
Antagonists
α2
Agonists
Antagonists
β
Agonists
Antagonists


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