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Details

Stereochemistry RACEMIC
Molecular Formula C14H12ClN3O3S
Molecular Weight 337.781
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of FENQUIZONE

SMILES

NS(=O)(=O)C1=CC2=C(NC(NC2=O)C3=CC=CC=C3)C=C1Cl

InChI

InChIKey=DBDTUXMDTSTPQZ-UHFFFAOYSA-N
InChI=1S/C14H12ClN3O3S/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/h1-7,13,17H,(H,18,19)(H2,16,20,21)

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 ( + / - )

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 Sat Dec 16 17:13:17 GMT 2023
Edited
by admin
on Sat Dec 16 17:13:17 GMT 2023
Record UNII
LJ1U13R8IK
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
FENQUIZONE
INN   MART.   MI   USAN   WHO-DD  
USAN   INN  
Official Name English
(±)-7-CHLORO-1,2,3,4-TETRAHYDRO-4-OXO-2-PHENYL-6-QUINAZOLINESULFONAMIDE
Systematic Name English
MG-13054
Code English
FENQUIZONE [MI]
Common Name English
6-QUINAZOLINESULFONAMIDE, 7-CHLORO-1,2,3,4-TETRAHYDRO-4-OXO-2-PHENYL-, (±)-
Systematic Name English
fenquizone [INN]
Common Name English
FENQUIZONE [MART.]
Common Name English
FENQUIZONE [USAN]
Common Name English
M.G. 13054
Code English
Fenquizone [WHO-DD]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C49185
Created by admin on Sat Dec 16 17:13:17 GMT 2023 , Edited by admin on Sat Dec 16 17:13:17 GMT 2023
WHO-ATC C03BA13
Created by admin on Sat Dec 16 17:13:17 GMT 2023 , Edited by admin on Sat Dec 16 17:13:17 GMT 2023
WHO-VATC QC03BA13
Created by admin on Sat Dec 16 17:13:17 GMT 2023 , Edited by admin on Sat Dec 16 17:13:17 GMT 2023
Code System Code Type Description
DRUG BANK
DB13708
Created by admin on Sat Dec 16 17:13:17 GMT 2023 , Edited by admin on Sat Dec 16 17:13:17 GMT 2023
PRIMARY
FDA UNII
LJ1U13R8IK
Created by admin on Sat Dec 16 17:13:17 GMT 2023 , Edited by admin on Sat Dec 16 17:13:17 GMT 2023
PRIMARY
EPA CompTox
DTXSID10864933
Created by admin on Sat Dec 16 17:13:17 GMT 2023 , Edited by admin on Sat Dec 16 17:13:17 GMT 2023
PRIMARY
INN
3444
Created by admin on Sat Dec 16 17:13:17 GMT 2023 , Edited by admin on Sat Dec 16 17:13:17 GMT 2023
PRIMARY
MESH
C007712
Created by admin on Sat Dec 16 17:13:17 GMT 2023 , Edited by admin on Sat Dec 16 17:13:17 GMT 2023
PRIMARY
PUBCHEM
68548
Created by admin on Sat Dec 16 17:13:17 GMT 2023 , Edited by admin on Sat Dec 16 17:13:17 GMT 2023
PRIMARY
ChEMBL
CHEMBL2106186
Created by admin on Sat Dec 16 17:13:17 GMT 2023 , Edited by admin on Sat Dec 16 17:13:17 GMT 2023
PRIMARY
SMS_ID
100000081487
Created by admin on Sat Dec 16 17:13:17 GMT 2023 , Edited by admin on Sat Dec 16 17:13:17 GMT 2023
PRIMARY
NCI_THESAURUS
C65670
Created by admin on Sat Dec 16 17:13:17 GMT 2023 , Edited by admin on Sat Dec 16 17:13:17 GMT 2023
PRIMARY
CAS
20287-37-0
Created by admin on Sat Dec 16 17:13:17 GMT 2023 , Edited by admin on Sat Dec 16 17:13:17 GMT 2023
PRIMARY
WIKIPEDIA
FENQUIZONE
Created by admin on Sat Dec 16 17:13:17 GMT 2023 , Edited by admin on Sat Dec 16 17:13:17 GMT 2023
PRIMARY
EVMPD
SUB07594MIG
Created by admin on Sat Dec 16 17:13:17 GMT 2023 , Edited by admin on Sat Dec 16 17:13:17 GMT 2023
PRIMARY
ECHA (EC/EINECS)
243-689-5
Created by admin on Sat Dec 16 17:13:17 GMT 2023 , Edited by admin on Sat Dec 16 17:13:17 GMT 2023
PRIMARY
MERCK INDEX
m1162
Created by admin on Sat Dec 16 17:13:17 GMT 2023 , Edited by admin on Sat Dec 16 17:13:17 GMT 2023
PRIMARY Merck Index
DRUG CENTRAL
1162
Created by admin on Sat Dec 16 17:13:17 GMT 2023 , Edited by admin on Sat Dec 16 17:13:17 GMT 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
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ACTIVE MOIETY