Substance

ID:700

Names and Identifiers
IUPAC Traditional name
acetazolamide
IUPAC name
N-(5-sulfamoyl-1,3,4-thiadiazol-2-yl)acetamide
Synonyms
AcetazolamideAcetazolamineCarbonic Anhydrase Inhibitor 6063AcetamidothiadiazolesulfonamideAcetazolamidAcetazolamide SodiumAcetazoleamideAcetozalamide
Brand Name
AcetazolamAtenezolDuiramidEdemoxFonuritStorzolamideGlaupaxNephramidNephramidePhonuritDazamideDiacarbDiamoxDiuramidDiuriwasDonmoxDiutazolEumictonAk-ZolCidamexDiureticum-HolzingerGlupaxNatrionexSk-AcetazolamideDiamox SequelsDiluranAcetamoxDiakarbApo-AcetazolamideDefiltranDehydratinDidocVetamox
Registration numbers
CAS Number
PubChem CID
PubChem SID
Properties
Physical Property
Solubility
0.98 mg/mL at 30 oC [YALKOWSKY,SH & DANNENFELSER,RM (1992)]
Hydrophobicity(logP)
-0.26 [HANSCH,C ET AL. (1995)]
Molecule Details
Drug Groups
approved
Description
One of the carbonic anhydrase inhibitors that is sometimes effective against absence seizures. It is sometimes useful also as an adjunct in the treatment of tonic-clonic, myoclonic, and atonic seizures, particularly in women whose seizures occur or are exacerbated at specific times in the menstrual cycle. However, its usefulness is transient often because of rapid development of tolerance. Its antiepileptic effect may be due to its inhibitory effect on brain carbonic anhydrase, which leads to an increased transneuronal chloride gradient, increased chloride current, and increased inhibition. (From Smith and Reynard, Textbook of Pharmacology, 1991, p337)
Indication
For adjunctive treatment of: edema due to congestive heart failure; drug-induced edema; centrencephalic epilepsies; chronic simple (open-angle) glaucoma
Pharmacology
Acetazolamide is a potent carbonic anhydrase inhibitor, effective in the control of fluid secretion, in the treatment of certain convulsive disorders and in the promotion of diuresis in instances of abnormal fluid retention. Acetazolamide is not a mercurial diuretic. Rather, it is a nonbacteriostatic sulfonamide possessing a chemical structure and pharmacological activity distinctly different from the bacteriostatic sulfonamides.
Affected Organisms
Humans and other mammals
Half Life
3 to 9 hours
Protein Binding
98%
External Links
Molecular Spectra
No Data Available
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References
No Data Available
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