Exaprolol

Exaprolol
Names
IUPAC name
1-(2-Cyclohexylphenoxy)-3-(propan-2-ylamino)propan-2-ol
Other names
Esprolol
Identifiers
3D model (JSmol)
ChemSpider
KEGG
UNII
Properties
C18H29NO2
Molar mass 291.435 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Exaprolol is a beta-adrenoceptor antagonist.[1]

Synthesis

Exaprolol synthesis[2]
gollark: https://a.osmarks.tk/www.computercraft.info/A/Main_Page.htmlmuahahahahaha.
gollark: Oh, I forgot the finish, oops.
gollark: Or even```rustfn main() { for i in 0..=10 { println!("{}", i); }}```
gollark: Although this really seems less clear than, say,```javascript-nodefor (let i = 0; i <= 10; i++) console.log(i)console.log("finish")```
gollark: Sorry, this is utterly incomprehensible to my feeble JS-using mind.

References

  1. Van Waarde, A; Doorduin, J; De Jong, JR; Dierckx, RA; Elsinga, PH (2008). "Synthesis and preliminary evaluation of (S)-11C-exaprolol, a novel beta-adrenoceptor ligand for PET". Neurochemistry International. 52 (4–5): 729–33. doi:10.1016/j.neuint.2007.09.009. PMID 17961850.
  2. Carissimi, M; Gentili, P; Grumelli, E; Milla, E; Picciola, G; Ravenna, F (1976). "Basic ethers of cyclohexylphenols with beta-blocking activity: Synthesis and pharmacological study of exaprolol". Arzneimittel-Forschung. 26 (4): 506–16. PMID 8056.


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