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Details

Stereochemistry RACEMIC
Molecular Formula C18H31N3O3
Molecular Weight 337.457
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PAFENOLOL

SMILES

CC(C)NCC(O)COC1=CC=C(CCNC(=O)NC(C)C)C=C1

InChI

InChIKey=PKWZWSXSCKVUJB-UHFFFAOYSA-N
InChI=1S/C18H31N3O3/c1-13(2)20-11-16(22)12-24-17-7-5-15(6-8-17)9-10-19-18(23)21-14(3)4/h5-8,13-14,16,20,22H,9-12H2,1-4H3,(H2,19,21,23)

HIDE SMILES / InChI

Molecular Formula C18H31N3O3
Molecular Weight 337.457
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Pafenolol is a beta 1 selective adrenoceptor blocker that was studied in phase I clinical trial in Sweden for the treatment of arrhythmia. However, this study was discontinued.

Approval Year

PubMed

PubMed

TitleDatePubMed
Pafenolol, a highly selective beta 1-adrenoceptor-antagonist, in asthmatic patients: interaction with terbutaline.
1983 Jan
Pafenolol in hypertension: a double-blind randomized trial of a new beta 1-selective adrenoceptor blocker.
1986 Jan-Feb
Evidence for an interaction between the beta-blocker pafenolol and bile salts in the intestinal lumen of the rat leading to dose-dependent oral absorption and double peaks in the plasma concentration-time profile.
1993 Jun
Dose-dependent intestinal absorption and significant intestinal excretion (exsorption) of the beta-blocker pafenolol in the rat.
1993 May
Patents

Sample Use Guides

Intravenous pafenolol (5 mg and 7.5 mg), metoprolol (15 mg), and saline were given double-blind at random and thereafter four increasing doses of terbutaline were given intravenously to seven asthmatic patients with reproducible reversibility of airways obstruction.
Route of Administration: Intravenous
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:40:58 GMT 2023
Edited
by admin
on Fri Dec 15 15:40:58 GMT 2023
Record UNII
5AEP5YJ9MZ
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PAFENOLOL
INN   WHO-DD  
INN  
Official Name English
UREA, N-(2-(4-(2-HYDROXY-3-((1-METHYLETHYL)AMINO)PROPOXY)PHENYL)ETHYL)-N'-(1-METHYLETHYL)-
Systematic Name English
UREA, N-(2-(4-(2-HYDROXY-3-((1-METHYLETHYL)AMINO)PROPOXY)PHENYL)ETHYL)-N'-(1-METHYLETHYL)-, (±)-
Common Name English
Pafenolol [WHO-DD]
Common Name English
(±)-1-(P-(2-HYDROXY-3-(ISOPROPYLAMINO)PROPOXY)PHENETHYL)-3-ISOPROPYLUREA
Common Name English
pafenolol [INN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C29576
Created by admin on Fri Dec 15 15:40:59 GMT 2023 , Edited by admin on Fri Dec 15 15:40:59 GMT 2023
Code System Code Type Description
NCI_THESAURUS
C66291
Created by admin on Fri Dec 15 15:40:59 GMT 2023 , Edited by admin on Fri Dec 15 15:40:59 GMT 2023
PRIMARY
ChEMBL
CHEMBL152371
Created by admin on Fri Dec 15 15:40:59 GMT 2023 , Edited by admin on Fri Dec 15 15:40:59 GMT 2023
PRIMARY
MESH
C036625
Created by admin on Fri Dec 15 15:40:59 GMT 2023 , Edited by admin on Fri Dec 15 15:40:59 GMT 2023
PRIMARY
CAS
83242-76-6
Created by admin on Fri Dec 15 15:40:59 GMT 2023 , Edited by admin on Fri Dec 15 15:40:59 GMT 2023
SUPERSEDED
SMS_ID
100000082778
Created by admin on Fri Dec 15 15:40:59 GMT 2023 , Edited by admin on Fri Dec 15 15:40:59 GMT 2023
PRIMARY
EPA CompTox
DTXSID20868386
Created by admin on Fri Dec 15 15:40:59 GMT 2023 , Edited by admin on Fri Dec 15 15:40:59 GMT 2023
PRIMARY
INN
5053
Created by admin on Fri Dec 15 15:40:59 GMT 2023 , Edited by admin on Fri Dec 15 15:40:59 GMT 2023
PRIMARY
EVMPD
SUB09585MIG
Created by admin on Fri Dec 15 15:40:59 GMT 2023 , Edited by admin on Fri Dec 15 15:40:59 GMT 2023
PRIMARY
FDA UNII
5AEP5YJ9MZ
Created by admin on Fri Dec 15 15:40:59 GMT 2023 , Edited by admin on Fri Dec 15 15:40:59 GMT 2023
PRIMARY
PUBCHEM
71144
Created by admin on Fri Dec 15 15:40:59 GMT 2023 , Edited by admin on Fri Dec 15 15:40:59 GMT 2023
PRIMARY
CAS
75949-61-0
Created by admin on Fri Dec 15 15:40:59 GMT 2023 , Edited by admin on Fri Dec 15 15:40:59 GMT 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY