Details
Stereochemistry | RACEMIC |
Molecular Formula | C9H12ClN3O4S2 |
Molecular Weight | 325.792 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CCC1NC2=CC(Cl)=C(C=C2S(=O)(=O)N1)S(N)(=O)=O
InChI
InChIKey=VXLCNTLWWUDBSO-UHFFFAOYSA-N
InChI=1S/C9H12ClN3O4S2/c1-2-9-12-6-3-5(10)7(18(11,14)15)4-8(6)19(16,17)13-9/h3-4,9,12-13H,2H2,1H3,(H2,11,14,15)
Molecular Formula | C9H12ClN3O4S2 |
Molecular Weight | 325.792 |
Charge | 0 |
Count |
|
Stereochemistry | RACEMIC |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Optical Activity | ( + / - ) |
DescriptionSources: http://www.google.je/patents/EP1125586A1?cl=en
Sources: http://www.google.je/patents/EP1125586A1?cl=en
Ethiazide is a diuretic.
Originator
Sources: http://www.google.je/patents/EP1125586A1?cl=en
Curator's Comment: Now is a part of Mitsubishi Tanabe Pharma.
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
Epimerization and racemization of some chiral drugs in the presence of cyclodextrin and liposomes. | 1989 Oct |
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Epimerization and racemization of some chiral drugs in the presence of human serum albumin. | 1990 Jan |
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Interaction of benzothiadiazides with human serum albumin studied by dialysis and spectroscopic methods. | 1994 Oct |
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 15:35:58 GMT 2023
by
admin
on
Fri Dec 15 15:35:58 GMT 2023
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Record UNII |
EK9LSW731R
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Record Status |
Validated (UNII)
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Record Version |
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NCI_THESAURUS |
C49185
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SUB07275MIG
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CHEMBL2106262
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C80840
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m723
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EK9LSW731R
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217-358-0
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Related Record | Type | Details | ||
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ENANTIOMER -> RACEMATE | |||
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ENANTIOMER -> RACEMATE |
Related Record | Type | Details | ||
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ACTIVE MOIETY |