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Ethoxzolamide

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
Ethoxzolamide
Clinical data
ATC code
  • None
Pharmacokinetic data
Protein binding~89%
Eliminationhalf-life2.5–5.5 hours
Identifiers
  • 6-Ethoxy-1,3-benzothiazole-2-sulfonamide
CAS Number
PubChemCID
IUPHAR/BPS
DrugBank
ChemSpider
UNII
KEGG
ChEBI
ChEMBL
CompTox Dashboard(EPA)
ECHA InfoCard100.006.546Edit this at Wikidata
Chemical and physical data
FormulaC9H10N2O3S2
Molar mass258.31 g·mol−1
3D model (JSmol)
  • O=S(=O)(c1nc2ccc(OCC)cc2s1)N
  • InChI=1S/C9H10N2O3S2/c1-2-14-6-3-4-7-8(5-6)15-9(11-7)16(10,12)13/h3-5H,2H2,1H3,(H2,10,12,13) checkY
  • Key:OUZWUKMCLIBBOG-UHFFFAOYSA-N checkY
  (verify)

Ethoxzolamide (alternatively known asethoxyzolamide) is asulfonamidemedication that functions as acarbonic anhydrase inhibitor.[1] It is used in the treatment ofglaucoma andduodenalulcers, and as adiuretic. It may also be used in the treatment of some forms ofepilepsy.

Pharmacology

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Ethoxzolamide, asulfonamide, inhibitscarbonic anhydrase activity in proximal renal tubules to decrease reabsorption of water, sodium, potassium, bicarbonate. It also decreases carbonic anhydrase in the CNS, increasing theseizure threshold. This reduction in carbonic anhydrase also reduces theintraocular pressure in the eye by decreasing aqueous humor.

Mechanism of action

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Ethoxzolamide binds and inhibits carbonic anhydrase I. Carbonic anhydrase plays an essential role in facilitating the transport ofcarbon dioxide and protons in theintracellular space, across biological membranes and in the layers of the extracellular space. The inhibition of thisenzyme effects the balance of applicable membrane equilibrium systems.

Synthesis

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Ethoxzolamide synthesis:GB 795174 ; J. Korman,U.S. patent 2,868,800 (1958, 1959 both toUpjohn).

See also

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References

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  1. ^Gordon DM (July 1958). "Ethoxzolamide; a new carbonic anhydrase inhibitor".American Journal of Ophthalmology.46 (1 Pt 1):41–4.doi:10.1016/S0002-9394(14)78070-5.PMID 13545308.
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