Ethoxzolamide drug data and news

Ethoxzolamide drug data, resources, and news articles (when available). Onconews.org provides news on cancer research. This section, which includes profiles on medicines that may or not be cancer-related is in beta form. If things run smoothly we will be releasing a new format late in the summer of 2006.

Generic name Ethoxzolamide
Brand Names/Synonyms Cardrase; Diuretic C; Ethamide; Ethoxazolamide; Ethoxyzolamide; Ethoxzolamide; Etoxzolamide; Glaucotensil; Redupresin; U-4191
Indication For use in the treatment of duodenal ulcers, as a diuretic, and in the treatment of glaucoma, and may also be useful in the treatment of seizures associated with epilepsy.
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Description Not Available
Pharmacology Ethoxzolamide, a sulfonamide, inhibits carbonic anhydrase activity in proximal renal tubules to decrease reabsorption of water, sodium, potassium, bicarbonate. It also decreases carbonic anhydrase in the CNS, increasing the seizure threshold. This reduction in carbonic anhydrase also reduces the intraocular pressure in the eye by decreasing aqueous humor.
Mechanism Of Action Ethoxzolamide binds and inhibits carbonic anhydrase I. Carbonic anhydrase plays an essential role in facilitating the transport of carbon dioxide and protons in the intracellular space, across biological membranes and in the layers of the extracellular space. The inhibition of this enzyme effects the balance of applicable membrane equilibrium systems.
Ethoxzolamide News
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Dosage Forms TABLET (125, 250 mg), CAPSULE (500mg), INJECTION (500mg)
Drug_Category Diuretics; Carbonic Anhydrase Inhibitors
Absorption Rapidly absorbed with 65% bioavailability
Interactions Interactions for Ethoxzolamide:
Ethoxzolamide may increase the action of tricyclics, amphetamines, procainamide, and quinidine. It may increase excretion of barbiturates, lithium, and ASA and may also increase the toxicity of salicylates. Coadministration of ethoxzolamide with other diuretics, amphotericin B, and corticosteroids may cause hypokalemia.
Toxicity Not Available
Organisms Affected Humans and other mammals
Chemical IUPAC Name 6-ethoxybenzothiazole-2-sulfonamide
Chemical Formula C9H10N2O3S2
Molecular Weight 258.319 g/mol
Smiles String CCOC1=CC2=C(C=C1)N=C(S2)S(=O)(=O)N
Melting Point 189 °C
Water Solubility 40 mg/L
State Solid
LogP/Hphobicity 1.218
Isoelectric Point Not Available
Biotransformation Not Available
Half Life 2.5-5.5 hours
Protein Binding [%] ~89%
RxList Link Not Available>RXlist
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Drug Reference Not Available
Drug Type Approved Drug
Accession No APRD00732
CAS Registry Number 452-35-7
KEGG Compound ID Not Available
PubChem ID SID:345073
PharmGKB ID Not Available
SwissProt ID Not Available
GenBank ID Not Available
Drug ID Number [DIN] Not Available

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