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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
MOL RATIO 1 MOL RATIO (average)
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Description

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

Primary TargetPharmacologyConditionPotency

Sample Use Guides

In Vivo Use Guide
Daily dose - 20 mg
Route of Administration: Oral
Substance Class Chemical
Record UNII
LJ1U13R8IK
Record Status Validated (UNII)
Record Version