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Details

Stereochemistry RACEMIC
Molecular Formula C24H30N2O4
Molecular Weight 410.506
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DRAQUINOLOL

SMILES

COC1=CC2=C(C=C1)C=C(N(C)C2=O)C3=CC=C(OCC(O)CNC(C)(C)C)C=C3

InChI

InChIKey=MZELTXWHFDTAOO-UHFFFAOYSA-N
InChI=1S/C24H30N2O4/c1-24(2,3)25-14-18(27)15-30-19-9-6-16(7-10-19)22-12-17-8-11-20(29-5)13-21(17)23(28)26(22)4/h6-13,18,25,27H,14-15H2,1-5H3

HIDE SMILES / InChI

Molecular Formula C24H30N2O4
Molecular Weight 410.506
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Draquinolol is a cardioselective beta-adrenoceptor antagonist with a long duration of action in vivo. The long duration of action of draquinolol in vivo is due to the formation of a tight complex with beta 1-adrenoceptors. Draquinolol reduced an exercise tachycardia.

Approval Year

PubMed

PubMed

TitleDatePubMed
The assessment in man of the beta-adrenoceptor blocking activity and cardioselectivity of H-I 42 BS, a long acting beta-adrenoceptor blocking drug.
1987 Apr

Sample Use Guides

Single dose - 400 mg
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:27:27 GMT 2023
Edited
by admin
on Fri Dec 15 16:27:27 GMT 2023
Record UNII
K3B3L3Q0GV
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
DRAQUINOLOL
INN   MART.  
INN  
Official Name English
3-(P-(3-(TERT-BUTYLAMINO)-2-HYDROXYPROPOXY)PHENYL)-7-METHOXY-2-METHYLISOCARBOSTYRIL
Common Name English
HI-42
Code English
DRAQUINOLOL [MART.]
Common Name English
1(2H)-ISOQUINOLINONE, 3-(4-(3-((1,1-DIMETHYLETHYL)AMINO)-2-HYDROXYPROPOXY)PHENYL)-7-METHOXY-2-METHYL-
Systematic Name English
H-I-42BS
Code English
draquinolol [INN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C29576
Created by admin on Fri Dec 15 16:27:27 GMT 2023 , Edited by admin on Fri Dec 15 16:27:27 GMT 2023
Code System Code Type Description
ChEMBL
CHEMBL1742429
Created by admin on Fri Dec 15 16:27:27 GMT 2023 , Edited by admin on Fri Dec 15 16:27:27 GMT 2023
PRIMARY
FDA UNII
K3B3L3Q0GV
Created by admin on Fri Dec 15 16:27:27 GMT 2023 , Edited by admin on Fri Dec 15 16:27:27 GMT 2023
PRIMARY
CAS
67793-71-9
Created by admin on Fri Dec 15 16:27:27 GMT 2023 , Edited by admin on Fri Dec 15 16:27:27 GMT 2023
PRIMARY
PUBCHEM
10070156
Created by admin on Fri Dec 15 16:27:27 GMT 2023 , Edited by admin on Fri Dec 15 16:27:27 GMT 2023
PRIMARY
NCI_THESAURUS
C65479
Created by admin on Fri Dec 15 16:27:27 GMT 2023 , Edited by admin on Fri Dec 15 16:27:27 GMT 2023
PRIMARY
EVMPD
SUB06397MIG
Created by admin on Fri Dec 15 16:27:27 GMT 2023 , Edited by admin on Fri Dec 15 16:27:27 GMT 2023
PRIMARY
EPA CompTox
DTXSID301024412
Created by admin on Fri Dec 15 16:27:27 GMT 2023 , Edited by admin on Fri Dec 15 16:27:27 GMT 2023
PRIMARY
INN
5869
Created by admin on Fri Dec 15 16:27:27 GMT 2023 , Edited by admin on Fri Dec 15 16:27:27 GMT 2023
PRIMARY
CAS
126522-41-6
Created by admin on Fri Dec 15 16:27:27 GMT 2023 , Edited by admin on Fri Dec 15 16:27:27 GMT 2023
SUPERSEDED
SMS_ID
100000080817
Created by admin on Fri Dec 15 16:27:27 GMT 2023 , Edited by admin on Fri Dec 15 16:27:27 GMT 2023
PRIMARY
WIKIPEDIA
Draquinolol
Created by admin on Fri Dec 15 16:27:27 GMT 2023 , Edited by admin on Fri Dec 15 16:27:27 GMT 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY