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Details

Stereochemistry RACEMIC
Molecular Formula C11H16ClN3O4S2
Molecular Weight 353.845
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BUTHIAZIDE

SMILES

CC(C)CC1NC2=CC(Cl)=C(C=C2S(=O)(=O)N1)S(N)(=O)=O

InChI

InChIKey=HGBFRHCDYZJRAO-UHFFFAOYSA-N
InChI=1S/C11H16ClN3O4S2/c1-6(2)3-11-14-8-4-7(12)9(20(13,16)17)5-10(8)21(18,19)15-11/h4-6,11,14-15H,3H2,1-2H3,(H2,13,16,17)

HIDE SMILES / InChI

Molecular Formula C11H16ClN3O4S2
Molecular Weight 353.845
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Buthiazide (or Butizide) is a diuretic of the thiazide class. It was used for the treatment of mild to moderate essential hypertension. Buthiazide reduces the reabsorption of electrolytes from the renal tubules. This results in increased excretion of water and electrolytes, including sodium, potassium, chloride, and magnesium. It is used in the treatment of several disorders including edema, hypertension, diabetes insipidus, and hypoparathyroidism.

Approval Year

PubMed

PubMed

TitleDatePubMed
Ex vivo antigen preparation for the serological detection of drug-dependent antibodies in immune haemolytic anaemias.
1984 Nov
Amlodipine/valsartan/hydrochlorothiazide: fixed-dose combination in hypertension.
2009
Renal and vascular glutathione S-transferase mu is not affected by pharmacological intervention to reduce systolic blood pressure.
2009 Aug
[Chlorthalidone better than hydrochlorothiazide in hypertension].
2010

Sample Use Guides

The combination of 100 mg spironolactone either with 5 mg bendrofluazide or with 10 mg butizide increased significantly the diuresis over the whole day.
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Fri Dec 15 19:07:01 GMT 2023
Edited
by admin
on Fri Dec 15 19:07:01 GMT 2023
Record UNII
W00SSD35VW
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
BUTHIAZIDE
MI   USAN  
USAN  
Official Name English
6-Chloro-3,4-dihydro-3-isobutyl-2H-1,2,4-benzothiadiazine-7-sulfonamide 1,1-dioxide
Systematic Name English
BUTHIAZIDE [MI]
Common Name English
BUTIZIDE [MART.]
Common Name English
butizide [INN]
Common Name English
BUTHIAZIDE [USAN]
Common Name English
ISOBUTYLHYDROCHLOROTHIAZIDE
Common Name English
Butizide [WHO-DD]
Common Name English
BUTIZIDE
INN   MART.   WHO-DD  
INN  
Official Name English
2H-1,2,4-BENZOTHIADIAZINE-7-SULFONAMIDE, 6-CHLORO-3,4-DIHYDRO-3-(2-METHYLPROPYL)-, 1,1-DIOXIDE
Systematic Name English
Classification Tree Code System Code
WHO-VATC QC03EA14
Created by admin on Fri Dec 15 19:07:01 GMT 2023 , Edited by admin on Fri Dec 15 19:07:01 GMT 2023
WHO-ATC C03EA14
Created by admin on Fri Dec 15 19:07:01 GMT 2023 , Edited by admin on Fri Dec 15 19:07:01 GMT 2023
Code System Code Type Description
DRUG CENTRAL
446
Created by admin on Fri Dec 15 19:07:01 GMT 2023 , Edited by admin on Fri Dec 15 19:07:01 GMT 2023
PRIMARY
FDA UNII
W00SSD35VW
Created by admin on Fri Dec 15 19:07:01 GMT 2023 , Edited by admin on Fri Dec 15 19:07:01 GMT 2023
PRIMARY
PUBCHEM
16274
Created by admin on Fri Dec 15 19:07:01 GMT 2023 , Edited by admin on Fri Dec 15 19:07:01 GMT 2023
PRIMARY
RXCUI
19882
Created by admin on Fri Dec 15 19:07:01 GMT 2023 , Edited by admin on Fri Dec 15 19:07:01 GMT 2023
PRIMARY RxNorm
EVMPD
SUB06024MIG
Created by admin on Fri Dec 15 19:07:01 GMT 2023 , Edited by admin on Fri Dec 15 19:07:01 GMT 2023
PRIMARY
NCI_THESAURUS
C171919
Created by admin on Fri Dec 15 19:07:01 GMT 2023 , Edited by admin on Fri Dec 15 19:07:01 GMT 2023
PRIMARY
MESH
C009732
Created by admin on Fri Dec 15 19:07:01 GMT 2023 , Edited by admin on Fri Dec 15 19:07:01 GMT 2023
PRIMARY
INN
1410
Created by admin on Fri Dec 15 19:07:01 GMT 2023 , Edited by admin on Fri Dec 15 19:07:01 GMT 2023
PRIMARY
WIKIPEDIA
BUTIZIDE
Created by admin on Fri Dec 15 19:07:01 GMT 2023 , Edited by admin on Fri Dec 15 19:07:01 GMT 2023
PRIMARY
EPA CompTox
DTXSID6022713
Created by admin on Fri Dec 15 19:07:01 GMT 2023 , Edited by admin on Fri Dec 15 19:07:01 GMT 2023
PRIMARY
MERCK INDEX
m2797
Created by admin on Fri Dec 15 19:07:01 GMT 2023 , Edited by admin on Fri Dec 15 19:07:01 GMT 2023
PRIMARY Merck Index
SMS_ID
100000088634
Created by admin on Fri Dec 15 19:07:01 GMT 2023 , Edited by admin on Fri Dec 15 19:07:01 GMT 2023
PRIMARY
CAS
2043-38-1
Created by admin on Fri Dec 15 19:07:01 GMT 2023 , Edited by admin on Fri Dec 15 19:07:01 GMT 2023
PRIMARY
ECHA (EC/EINECS)
218-048-8
Created by admin on Fri Dec 15 19:07:01 GMT 2023 , Edited by admin on Fri Dec 15 19:07:01 GMT 2023
PRIMARY
ChEMBL
CHEMBL2104197
Created by admin on Fri Dec 15 19:07:01 GMT 2023 , Edited by admin on Fri Dec 15 19:07:01 GMT 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY