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Pargolol

From Wikipedia, the free encyclopedia
Pargolol
Names
IUPAC name
1-(tert-Butylamino)-3-(2-prop-2-ynoxyphenoxy)propan-2-ol
Identifiers
3D model (JSmol)
ChemSpider
UNII
  • InChI=1S/C16H23NO3/c1-5-10-19-14-8-6-7-9-15(14)20-12-13(18)11-17-16(2,3)4/h1,6-9,13,17-18H,10-12H2,2-4H3
    Key: UFNAECVCKNHAKN-UHFFFAOYSA-N
  • InChI=1/C16H23NO3/c1-5-10-19-14-8-6-7-9-15(14)20-12-13(18)11-17-16(2,3)4/h1,6-9,13,17-18H,10-12H2,2-4H3
    Key: UFNAECVCKNHAKN-UHFFFAOYAZ
  • CC(C)(C)NCC(COC1=CC=CC=C1OCC#C)O
Properties
C16H23NO3
Molar mass277.364 g·mol−1
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
Chemical compound

Pargolol is abeta adrenergic receptor antagonist.[1]

References

[edit]
  1. ^Hugues, FC; Julien, D; Bors, V; Mougeot, G; Marche, J (1980). "Determination in man of the beta blocking properties and the pharmacological half of pargolol (Author's transl)".Thérapie.35 (4):475–81.PMID 6110251.
α1
Agonists
Antagonists
α2
Agonists
Antagonists
β
Agonists
Antagonists


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