物质信息

ID:700

名称和标识
IUPAC传统名
acetazolamide
IUPAC标准名
N-(5-sulfamoyl-1,3,4-thiadiazol-2-yl)acetamide
别名
AcetazolamideAcetazolamineCarbonic Anhydrase Inhibitor 6063AcetamidothiadiazolesulfonamideAcetazolamidAcetazolamide SodiumAcetazoleamideAcetozalamide
商标名
AcetazolamAtenezolDuiramidEdemoxFonuritStorzolamideGlaupaxNephramidNephramidePhonuritDazamideDiacarbDiamoxDiuramidDiuriwasDonmoxDiutazolEumictonAk-ZolCidamexDiureticum-HolzingerGlupaxNatrionexSk-AcetazolamideDiamox SequelsDiluranAcetamoxDiakarbApo-AcetazolamideDefiltranDehydratinDidocVetamox
数据登录号
CAS号
PubChem CID
PubChem SID
化合物性质
理化性质
疏水性(logP)
-0.26 [HANSCH,C ET AL. (1995)]
溶解度
0.98 mg/mL at 30 oC [YALKOWSKY,SH & DANNENFELSER,RM (1992)]
描述信息
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%
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