B7149
Benzthiazide
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About This Item
Empirical Formula (Hill Notation):
C15H14ClN3O4S3
CAS Number:
Molecular Weight:
431.94
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
form
solid
Quality Level
SMILES string
NS(=O)(=O)c1cc2c(NC(CSCc3ccccc3)=NS2(=O)=O)cc1Cl
InChI
1S/C15H14ClN3O4S3/c16-11-6-12-14(7-13(11)25(17,20)21)26(22,23)19-15(18-12)9-24-8-10-4-2-1-3-5-10/h1-7H,8-9H2,(H,18,19)(H2,17,20,21)
InChI key
NDTSRXAMMQDVSW-UHFFFAOYSA-N
Gene Information
human ... SLC12A3(6559)
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Related Categories
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Resp. Sens. 1 - Skin Sens. 1
Storage Class Code
11 - Combustible Solids
WGK
WGK 2
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
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Thiazides XIII: Dissolution testing: a bioavailability predictor for benzthiazide tablets.
V P Shah et al.
Biopharmaceutics & drug disposition, 3(3), 283-285 (1982-07-01)
L R Berkowitz
The American journal of physiology, 258(4 Pt 1), C622-C629 (1990-04-01)
The thioalkylating agent N-ethylmaleimide (NEM) causes ouabain-insensitive K loss from human red blood cells. This K loss is inhibited when intracellular Cl is replaced by another permeant anion or when loop diuretics are placed in the incubation medium after NEM
Laurie De Wilde et al.
Journal of chromatography. A, 1579, 31-40 (2018-11-16)
Diuretics can be misused to force diuresis to achieve weight loss or to mask the intake of a prohibited substance and are therefore prohibited by the World Anti-Doping Agency (WADA). For similar reasons other masking agents (vaptans, probenecid, etc.) are
J P Huang et al.
Journal of analytical toxicology, 23(5), 337-342 (1999-09-17)
This study describes a matrix-assisted laser-desorption-ionization (MALDI) mass spectrometry for rapid screening of 12 diuretics in spiked urine. C60 is used as the matrix for MALDI. Diuretics are directly analyzed by C60-MALDI without previous derivatization. The fact that most diuretic
Hee Sook Lee et al.
BMC systems biology, 6, 80-80 (2012-07-04)
The process of drug discovery and development is time-consuming and costly, and the probability of success is low. Therefore, there is rising interest in repositioning existing drugs for new medical indications. When successful, this process reduces the risk of failure
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