U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry RACEMIC
Molecular Formula C14H18N2O2
Molecular Weight 246.3049
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of QUINTERENOL

SMILES

CC(C)NCC(O)C1=C2C=CC=NC2=C(O)C=C1

InChI

InChIKey=RSDQHEMTUCMUPQ-UHFFFAOYSA-N
InChI=1S/C14H18N2O2/c1-9(2)16-8-13(18)10-5-6-12(17)14-11(10)4-3-7-15-14/h3-7,9,13,16-18H,8H2,1-2H3

HIDE SMILES / InChI

Molecular Formula C14H18N2O2
Molecular Weight 246.3049
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Quinterenol is a substituted 8-hydroxyquinoline derivative patented by Pfizer, Chas., and Co., Inc. as a bronchodilator. Quinterenol acts as a beta-adrenergic agonist that increased ventricular rate in most of the experimental animals.

Approval Year

PubMed

PubMed

TitleDatePubMed
Bronchodilator effects of Quinterenol sulfate--a preliminary clinical study.
1969-01-01
Patents

Patents

Sample Use Guides

0.4 mg
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Mon Mar 31 17:55:49 GMT 2025
Edited
by admin
on Mon Mar 31 17:55:49 GMT 2025
Record UNII
100EPZ8Y7G
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
QUINTERENOL
Common Name English
QUINPRENALINE
INN  
INN  
Preferred Name English
8-HYDROXY-.ALPHA.-((ISOPROPYLAMINO)METHYL)-5-QUINOLINEMETHANOL
Systematic Name English
DL-5-(1-HYDROXY-2-ISOPROPYLAMINOETHYL)-8-HYDROXYQUINOLINE
Common Name English
quinprenaline [INN]
Common Name English
(±)-QUINTERENOL
Common Name English
5-QUINOLINEMETHANOL, 8-HYDROXY-.ALPHA.-(((1-METHYLETHYL)AMINO)METHYL)-
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C319
Created by admin on Mon Mar 31 17:55:49 GMT 2025 , Edited by admin on Mon Mar 31 17:55:49 GMT 2025
Code System Code Type Description
MESH
C100139
Created by admin on Mon Mar 31 17:55:49 GMT 2025 , Edited by admin on Mon Mar 31 17:55:49 GMT 2025
PRIMARY
EPA CompTox
DTXSID70864439
Created by admin on Mon Mar 31 17:55:49 GMT 2025 , Edited by admin on Mon Mar 31 17:55:49 GMT 2025
PRIMARY
ChEMBL
CHEMBL2009119
Created by admin on Mon Mar 31 17:55:49 GMT 2025 , Edited by admin on Mon Mar 31 17:55:49 GMT 2025
PRIMARY
PUBCHEM
26258
Created by admin on Mon Mar 31 17:55:49 GMT 2025 , Edited by admin on Mon Mar 31 17:55:49 GMT 2025
PRIMARY
CAS
28143-90-0
Created by admin on Mon Mar 31 17:55:49 GMT 2025 , Edited by admin on Mon Mar 31 17:55:49 GMT 2025
SUPERSEDED
NCI_THESAURUS
C152130
Created by admin on Mon Mar 31 17:55:49 GMT 2025 , Edited by admin on Mon Mar 31 17:55:49 GMT 2025
PRIMARY
CAS
13757-97-6
Created by admin on Mon Mar 31 17:55:49 GMT 2025 , Edited by admin on Mon Mar 31 17:55:49 GMT 2025
PRIMARY
EVMPD
SUB10222MIG
Created by admin on Mon Mar 31 17:55:49 GMT 2025 , Edited by admin on Mon Mar 31 17:55:49 GMT 2025
PRIMARY
FDA UNII
100EPZ8Y7G
Created by admin on Mon Mar 31 17:55:49 GMT 2025 , Edited by admin on Mon Mar 31 17:55:49 GMT 2025
PRIMARY
INN
2291
Created by admin on Mon Mar 31 17:55:49 GMT 2025 , Edited by admin on Mon Mar 31 17:55:49 GMT 2025
PRIMARY
SMS_ID
100000080301
Created by admin on Mon Mar 31 17:55:49 GMT 2025 , Edited by admin on Mon Mar 31 17:55:49 GMT 2025
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
ENANTIOMER -> RACEMATE
SALT/SOLVATE -> PARENT
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY