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Details

Stereochemistry RACEMIC
Molecular Formula C11H14ClN3O4S3
Molecular Weight 383.895
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of Althiazide

SMILES

NS(=O)(=O)C1=C(Cl)C=C2NC(CSCC=C)NS(=O)(=O)C2=C1

InChI

InChIKey=VGLGVJVUHYTIIU-UHFFFAOYSA-N
InChI=1S/C11H14ClN3O4S3/c1-2-3-20-6-11-14-8-4-7(12)9(21(13,16)17)5-10(8)22(18,19)15-11/h2,4-5,11,14-15H,1,3,6H2,(H2,13,16,17)

HIDE SMILES / InChI

Molecular Formula C11H14ClN3O4S3
Molecular Weight 383.895
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Altizide, a thiazide diuretic, and aldosterone antagonist, in combination with spironolactone was marketed under brand name Aldactazine to treat patients with mild to moderate hypertension. In addition, Aldactazine was investigated for the treatment of congestive cardiac insufficiency.

Approval Year

PubMed

PubMed

TitleDatePubMed
Generic sample preparation combined with high-resolution liquid chromatography-time-of-flight mass spectrometry for unification of urine screening in doping-control laboratories.
2010-04
Probing the allosteric modulator binding site of GluR2 with thiazide derivatives.
2009-09-15
Detection of urinary markers for thiazide diuretics after oral administration of hydrochlorothiazide and altizide-relevance to doping control analysis.
2009-03-20
Stability of selected chlorinated thiazide diuretics.
2009-02-20
A case of brucellar spondylodiscitis involving the cervical spine.
2009
Mechanism of [m+h]+ formation in atmospheric pressure photoionization mass spectrometry: identification of propionitrile in acetonitrile with high mass accuracy measurement and tandem mass spectrometry and evidence for its involvement in the protonation phenomenon.
2008-11
Fast gas chromatographic/mass spectrometric determination of diuretics and masking agents in human urine: Development and validation of a productive screening protocol for antidoping analysis.
2006-12-01
High-speed gas chromatography in doping control: fast-GC and fast-GC/MS determination of beta-adrenoceptor ligands and diuretics.
2006-12
Synthesis and application of mono-2A-azido-2A-deoxyperphenylcarbamoylated beta-cyclodextrin and mono-2A-azido-2A-deoxyperacetylated beta-cyclodextrin as chiral stationary phases for high-performance liquid chromatography.
2006-01-06
Effects of pH and the presence of micelles on the resolution of diuretics by reversed-phase liquid chromatography.
2004-01-02
[Management of bronchiolitis in the infant. Recommendations. Long text].
2001-01

Sample Use Guides

Aldactazine ( 25 mg spironolactone and 15 mg altizide, 1/day)
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:22:02 GMT 2025
Edited
by admin
on Mon Mar 31 18:22:02 GMT 2025
Record UNII
GI8CB72B0D
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
Altizide
EP   INN   MART.   WHO-DD  
INN  
Preferred Name English
Althiazide
MI   USAN  
USAN  
Official Name English
ALTHIAZIDE [USAN]
Common Name English
NSC-757786
Code English
Altizide [WHO-DD]
Common Name English
altizide [INN]
Common Name English
ALTIZIDE [MART.]
Common Name English
2H-1,2,4-Benzothiadiazine-7-sulfonamide, 6-chloro-3,4-dihydro-3-[(2-propen-1-ylthio)methyl]-, 1,1-dioxide
Systematic Name English
3-[(Allylthio)methyl]-6-chloro-3,4-dihydro-2H-1,2,4-benzothiadiazine-7-sulfonamide 1,1-dioxide
Systematic Name English
ALTIZIDE [EP IMPURITY]
Common Name English
ALTIZIDE [EP MONOGRAPH]
Common Name English
P-1779
Code English
Classification Tree Code System Code
WHO-VATC QC03EA04
Created by admin on Mon Mar 31 18:22:02 GMT 2025 , Edited by admin on Mon Mar 31 18:22:02 GMT 2025
NCI_THESAURUS C49185
Created by admin on Mon Mar 31 18:22:02 GMT 2025 , Edited by admin on Mon Mar 31 18:22:02 GMT 2025
WHO-ATC C03EA04
Created by admin on Mon Mar 31 18:22:02 GMT 2025 , Edited by admin on Mon Mar 31 18:22:02 GMT 2025
Code System Code Type Description
EVMPD
SUB05379MIG
Created by admin on Mon Mar 31 18:22:02 GMT 2025 , Edited by admin on Mon Mar 31 18:22:02 GMT 2025
PRIMARY
MERCK INDEX
m1584
Created by admin on Mon Mar 31 18:22:02 GMT 2025 , Edited by admin on Mon Mar 31 18:22:02 GMT 2025
PRIMARY Merck Index
PUBCHEM
2122
Created by admin on Mon Mar 31 18:22:02 GMT 2025 , Edited by admin on Mon Mar 31 18:22:02 GMT 2025
PRIMARY
ChEMBL
CHEMBL599870
Created by admin on Mon Mar 31 18:22:02 GMT 2025 , Edited by admin on Mon Mar 31 18:22:02 GMT 2025
PRIMARY
INN
1382
Created by admin on Mon Mar 31 18:22:02 GMT 2025 , Edited by admin on Mon Mar 31 18:22:02 GMT 2025
PRIMARY
RXCUI
17599
Created by admin on Mon Mar 31 18:22:02 GMT 2025 , Edited by admin on Mon Mar 31 18:22:02 GMT 2025
PRIMARY RxNorm
DRUG CENTRAL
140
Created by admin on Mon Mar 31 18:22:02 GMT 2025 , Edited by admin on Mon Mar 31 18:22:02 GMT 2025
PRIMARY
EPA CompTox
DTXSID3045857
Created by admin on Mon Mar 31 18:22:02 GMT 2025 , Edited by admin on Mon Mar 31 18:22:02 GMT 2025
PRIMARY
CAS
5588-16-9
Created by admin on Mon Mar 31 18:22:02 GMT 2025 , Edited by admin on Mon Mar 31 18:22:02 GMT 2025
PRIMARY
ECHA (EC/EINECS)
226-994-8
Created by admin on Mon Mar 31 18:22:02 GMT 2025 , Edited by admin on Mon Mar 31 18:22:02 GMT 2025
PRIMARY
FDA UNII
GI8CB72B0D
Created by admin on Mon Mar 31 18:22:02 GMT 2025 , Edited by admin on Mon Mar 31 18:22:02 GMT 2025
PRIMARY
NSC
757786
Created by admin on Mon Mar 31 18:22:02 GMT 2025 , Edited by admin on Mon Mar 31 18:22:02 GMT 2025
PRIMARY
SMS_ID
100000092140
Created by admin on Mon Mar 31 18:22:02 GMT 2025 , Edited by admin on Mon Mar 31 18:22:02 GMT 2025
PRIMARY
NCI_THESAURUS
C80838
Created by admin on Mon Mar 31 18:22:02 GMT 2025 , Edited by admin on Mon Mar 31 18:22:02 GMT 2025
PRIMARY
MESH
C006480
Created by admin on Mon Mar 31 18:22:02 GMT 2025 , Edited by admin on Mon Mar 31 18:22:02 GMT 2025
PRIMARY
WIKIPEDIA
ALTIZIDE
Created by admin on Mon Mar 31 18:22:02 GMT 2025 , Edited by admin on Mon Mar 31 18:22:02 GMT 2025
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (TLC)
EP
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Related Record Type Details
ACTIVE MOIETY