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Flag Counter
  2. World Encyclopedia
  3. Procinolol - Wikipedia
Procinolol - Wikipedia
From Wikipedia, the free encyclopedia
Procinolol
Names
IUPAC name
1-(2-Cyclopropylphenoxy)-3-(propan-2-ylamino)propan-2-ol
Identifiers
ChemSpider
UNII
  • InChI=1S/C15H23NO2/c1-11(2)16-9-13(17)10-18-15-6-4-3-5-14(15)12-7-8-12/h3-6,11-13,16-17H,7-10H2,1-2H3
    Key: RTAGQMIEWAAKMO-UHFFFAOYSA-N
  • InChI=1/C15H23NO2/c1-11(2)16-9-13(17)10-18-15-6-4-3-5-14(15)12-7-8-12/h3-6,11-13,16-17H,7-10H2,1-2H3
    Key: RTAGQMIEWAAKMO-UHFFFAOYAR
Properties
C15H23NO2
Molar mass 249.354 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Procinolol is a beta adrenergic receptor antagonist, a group of pharmaceutical drugs that lower heart rhythm and blood pressure.[1]

It is not known to be marketed anywhere in the world in 2021.[2]

References

  1. ^ Singh, KP (1983). "Influence of beta-adrenoceptor antagonists on spontaneous rate and on force of contraction of isolated rabbit atria". Indian Journal of Physiology and Pharmacology. 27 (4): 311–6. PMID 6146567.
  2. ^ "Procinolol search results". Drugs.com. Retrieved 2021-03-31.


Stub icon

This drug article relating to the cardiovascular system is a stub. You can help Wikipedia by adding missing information.

Sunting pranala
url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url 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