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Details

Stereochemistry RACEMIC
Molecular Formula C17H26N2O3
Molecular Weight 306.3999
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of SOQUINOLOL

SMILES

CC(C)(C)NCC(O)COC1=CC=CC2=C1CCN(C2)C=O

InChI

InChIKey=GMJHUSJLZXFFQJ-UHFFFAOYSA-N
InChI=1S/C17H26N2O3/c1-17(2,3)18-9-14(21)11-22-16-6-4-5-13-10-19(12-20)8-7-15(13)16/h4-6,12,14,18,21H,7-11H2,1-3H3

HIDE SMILES / InChI

Molecular Formula C17H26N2O3
Molecular Weight 306.3999
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Soquinolol [WE 704] is a β-blocker that was under clinical development for the treatment of heart failure, but this research was discontinued. Soquinolol is a highly potent non-subtype-selective beta-adrenergic receptor blocker, which is devoid of any intrinsic sympathomimetic activity. Its local anaesthetic activity (membrane stabilizing effect) is very weak. It also shows good enteral efficacy and long duration of action. In binding studies with heart (Ki beta 1 = 3.25 nmol/l) and lung membranes (Ki beta 2 = 0.85 nmol/l) its binding profile was found to be similar to that of propranolol.

Approval Year

PubMed

PubMed

TitleDatePubMed
Patents

Patents

Sample Use Guides

In the conscious dog soquinolol's beta 1-adrenergic blocking activity (ED 50%) on intravenous injection (5.5 ug/kg) and oral administration (5.8 ug/kg) is about twice as great as that of pindolol and 19 times (i.v.) or 138 times (p.o.) greater than that of propranolol.
Route of Administration: Other
In Vitro Use Guide
In binding studies with heart (Ki beta 1 = 3.25 nmol/l) and lung membranes (Ki beta 2 = 0.85 nmol/l) Soquinolol's binding profile was found to be similar to that of propranolol. Soquinolol inhibits the isoprenaline-induced tachycardia (EC50% = 48 ug/l) in the guinea-pig Langendorff heart in vitro.
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:05:48 GMT 2023
Edited
by admin
on Fri Dec 15 16:05:48 GMT 2023
Record UNII
15CC9BOH7Q
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
SOQUINOLOL
INN  
INN  
Official Name English
Soquinolol [WHO-DD]
Common Name English
soquinolol [INN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C29576
Created by admin on Fri Dec 15 16:05:48 GMT 2023 , Edited by admin on Fri Dec 15 16:05:48 GMT 2023
Code System Code Type Description
CAS
61563-18-6
Created by admin on Fri Dec 15 16:05:48 GMT 2023 , Edited by admin on Fri Dec 15 16:05:48 GMT 2023
PRIMARY
ECHA (EC/EINECS)
262-844-8
Created by admin on Fri Dec 15 16:05:48 GMT 2023 , Edited by admin on Fri Dec 15 16:05:48 GMT 2023
PRIMARY
ChEMBL
CHEMBL1742453
Created by admin on Fri Dec 15 16:05:48 GMT 2023 , Edited by admin on Fri Dec 15 16:05:48 GMT 2023
PRIMARY
MESH
C058571
Created by admin on Fri Dec 15 16:05:48 GMT 2023 , Edited by admin on Fri Dec 15 16:05:48 GMT 2023
PRIMARY
PUBCHEM
68811
Created by admin on Fri Dec 15 16:05:48 GMT 2023 , Edited by admin on Fri Dec 15 16:05:48 GMT 2023
PRIMARY
NCI_THESAURUS
C73019
Created by admin on Fri Dec 15 16:05:48 GMT 2023 , Edited by admin on Fri Dec 15 16:05:48 GMT 2023
PRIMARY
FDA UNII
15CC9BOH7Q
Created by admin on Fri Dec 15 16:05:48 GMT 2023 , Edited by admin on Fri Dec 15 16:05:48 GMT 2023
PRIMARY
SMS_ID
100000083790
Created by admin on Fri Dec 15 16:05:48 GMT 2023 , Edited by admin on Fri Dec 15 16:05:48 GMT 2023
PRIMARY
EVMPD
SUB10594MIG
Created by admin on Fri Dec 15 16:05:48 GMT 2023 , Edited by admin on Fri Dec 15 16:05:48 GMT 2023
PRIMARY
INN
4761
Created by admin on Fri Dec 15 16:05:48 GMT 2023 , Edited by admin on Fri Dec 15 16:05:48 GMT 2023
PRIMARY
WIKIPEDIA
Soquinolol
Created by admin on Fri Dec 15 16:05:48 GMT 2023 , Edited by admin on Fri Dec 15 16:05:48 GMT 2023
PRIMARY
EPA CompTox
DTXSID00866865
Created by admin on Fri Dec 15 16:05:48 GMT 2023 , Edited by admin on Fri Dec 15 16:05:48 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY