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Cyanopindolol

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
Cyanopindolol
Skeletal formula of cyanopindolol
Space-filling model of the cyanopindolol molecule
Clinical data
ATC code
  • none
Identifiers
  • (RS)-4-[3-(tert-Butylamino)-2-hydroxypropoxy]-1H-indole-2-carbonitrile
CAS Number
PubChemCID
IUPHAR/BPS
ChemSpider
UNII
ChEMBL
PDB ligand
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC16H21N3O2
Molar mass287.363 g·mol−1
3D model (JSmol)
ChiralityRacemic mixture
  • N#CC1=CC2=C(OCC(CNC(C)(C)C)O)C=CC=C2N1
  • InChI=1S/C16H21N3O2/c1-16(2,3)18-9-12(20)10-21-15-6-4-5-14-13(15)7-11(8-17)19-14/h4-7,12,18-20H,9-10H2,1-3H3 ☒N
  • Key:QXIUMMLTJVHILT-UHFFFAOYSA-N ☒N
 ☒NcheckY (what is this?)  (verify)

Cyanopindolol is a drug related topindolol which acts as both aβ1 adrenoceptorantagonist and a5-HT1A receptor antagonist. Itsradiolabelled derivativeiodocyanopindolol has been widely used in mapping the distribution of beta adrenoreceptors in the body.[1]

References

[edit]
  1. ^Hoyer D, Engel G (1983). "Binding of 125I-cyanopindolol to beta-1-adrenoceptors in a high and low affinity state".Journal of Receptor Research.3 (1–2):45–59.doi:10.3109/10799898309041922.PMID 6304308.
β, non-selective
β1-selective
β2-selective
α1- + β-selective
α1
Agonists
Antagonists
α2
Agonists
Antagonists
β
Agonists
Antagonists
5-HT1
5-HT1A
5-HT1B
5-HT1D
5-HT1E
5-HT1F
5-HT2
5-HT2A
5-HT2B
5-HT2C
5-HT37
5-HT3
5-HT4
5-HT5A
5-HT6
5-HT7
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