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Details

Stereochemistry RACEMIC
Molecular Formula C14H11ClN3O3S.K
Molecular Weight 375.872
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of FENQUIZONE POTASSIUM

SMILES

[K+].[NH-]S(=O)(=O)C1=CC2=C(NC(NC2=O)C3=CC=CC=C3)C=C1Cl

InChI

InChIKey=SOOGHCNPHWQISK-UHFFFAOYSA-M
InChI=1S/C14H12ClN3O3S.K/c15-10-7-11-9(6-12(10)22(16,20)21)14(19)18-13(17-11)8-4-2-1-3-5-8;/h1-7,13H,(H4,16,17,18,19,20,21);/q;+1/p-1

HIDE SMILES / InChI

Molecular Formula C14H12ClN3O3S
Molecular Weight 337.781
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Molecular Formula K
Molecular Weight 39.0983
Charge 1
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Fenquizone is the diuretic drug. The distribution of fenquizone labelled with 14C in mice was studied by means of an autoradiographic technique. High concentration of radioactivity was found in the intestine, liver, kidney, blood, myocardium and skeletal muscles in decreasing order at various times after oral administration. The labelled compound did not cross the blood-brain barrier. Fenquizone is a saluretic with a quinazolone structure which acts by blocking reabsorption of sodium in the proximal tubule and the ascending branch of the loop of Henle, as well as in the proximal section of the convoluted distal tubule. At low doses fenquizone has an hypotensive action without showing the characteristics secondary effects of diuretics so that it can be employed for long-term treatments without any risk. Fenquizone showed also a significant decrease of symptoms (headache, dizziness) due to hypertension. No undesirable side effects were observed.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency

Sample Use Guides

Daily dose - 20 mg
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Fri Dec 15 18:55:50 UTC 2023
Edited
by admin
on Fri Dec 15 18:55:50 UTC 2023
Record UNII
1O41UTO57H
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
FENQUIZONE POTASSIUM
MART.   WHO-DD  
Common Name English
7-CHLORO-1,2,3,4-TETRAHYDRO-4-OXO-2-PHENYL-6-QUINAZOLINESULFONAMIDE MONOPOTASSIUM SALT
Common Name English
FENQUIZONE MONOPOTASSIUM SALT [MI]
Common Name English
FENQUIZONE MONOPOTASSIUM SALT
MI  
Common Name English
FENQUIZONE MONOPOTASSIUM
Common Name English
FENQUIZONE POTASSIUM [MART.]
Common Name English
Fenquizone potassium [WHO-DD]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C49185
Created by admin on Fri Dec 15 18:55:50 UTC 2023 , Edited by admin on Fri Dec 15 18:55:50 UTC 2023
Code System Code Type Description
NCI_THESAURUS
C95125
Created by admin on Fri Dec 15 18:55:50 UTC 2023 , Edited by admin on Fri Dec 15 18:55:50 UTC 2023
PRIMARY
SMS_ID
100000086966
Created by admin on Fri Dec 15 18:55:50 UTC 2023 , Edited by admin on Fri Dec 15 18:55:50 UTC 2023
PRIMARY
FDA UNII
1O41UTO57H
Created by admin on Fri Dec 15 18:55:50 UTC 2023 , Edited by admin on Fri Dec 15 18:55:50 UTC 2023
PRIMARY
MERCK INDEX
m1162
Created by admin on Fri Dec 15 18:55:50 UTC 2023 , Edited by admin on Fri Dec 15 18:55:50 UTC 2023
PRIMARY Merck Index
CAS
52246-40-9
Created by admin on Fri Dec 15 18:55:50 UTC 2023 , Edited by admin on Fri Dec 15 18:55:50 UTC 2023
PRIMARY
EVMPD
SUB02127MIG
Created by admin on Fri Dec 15 18:55:50 UTC 2023 , Edited by admin on Fri Dec 15 18:55:50 UTC 2023
PRIMARY
PUBCHEM
91663265
Created by admin on Fri Dec 15 18:55:50 UTC 2023 , Edited by admin on Fri Dec 15 18:55:50 UTC 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY