Details
Stereochemistry | RACEMIC |
Molecular Formula | C10H12ClN3O6S2 |
Molecular Weight | 369.802 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
COC(=O)C1NC2=C(C=C(C(Cl)=C2)S(N)(=O)=O)S(=O)(=O)N1C
InChI
InChIKey=PFRBORHNFYMVOA-UHFFFAOYSA-N
InChI=1S/C10H12ClN3O6S2/c1-14-9(10(15)20-2)13-6-3-5(11)7(21(12,16)17)4-8(6)22(14,18)19/h3-4,9,13H,1-2H3,(H2,12,16,17)
Molecular Formula | C10H12ClN3O6S2 |
Molecular Weight | 369.802 |
Charge | 0 |
Count |
|
Stereochemistry | RACEMIC |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Optical Activity | ( + / - ) |
Carmetizide is benzothiadiazine derivative patented by pharmaceutical company Abbott Laboratories as a diuretic. In preclinical studies, Carmetizide demonstrates perfect safety profile. Administration of Carmetizide (10,000 mg/kg, orally or 5000 mg/kg, s.c. or i.p.) to rats had no toxic effect. Carmetizide had no effect on the central nervous system and the cardiovascular system of guinea pigs or on the heart-lung preparation of dogs. These drugs did not affect the body temperature of rats and the blood coagulation of rabbits. Carmetizide had no effect on the spontaneous movement of smooth muscles.
Approval Year
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 16:24:03 GMT 2023
by
admin
on
Fri Dec 15 16:24:03 GMT 2023
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Record UNII |
8695816VMO
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Record Status |
Validated (UNII)
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Record Version |
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DTXSID20866100
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CHEMBL2104012
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8695816VMO
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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 |