Methazolamide

CHEMBL19 Phase 4 Aprobado Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
236.3 g/mol
LogP
0.1
Phase
4

A carbonic anhydrase inhibitor used to lower elevated intraocular (eye) pressure in people with glaucoma who cannot tolerate or do not respond adequately to other treatments. It helps prevent vision loss by reducing fluid buildup in the eye.

Peso molecular

236,3000 g/mol

LogP

0,10

TPSA

139,00 Ų

Regla de cinco de Lipinski

Cumple

Áreas terapéuticas

Mecanismo de acción

Selectively blocks angiotensin II type 1 (AT1) receptors, preventing the vasoconstrictive and aldosterone-secreting effects of angiotensin II. This results in vasodilation, reduced sodium retention, and decreased blood pressure.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Mecanismo

Selectively blocks angiotensin II type 1 (AT1) receptors, preventing the vasoconstrictive and aldosterone-secreting effects of angiotensin II. This results in vasodilation, reduced sodium retention, and decreased blood pressure.

Estructura 2D

SVG PNG

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SMILES

CC(=O)/N=c1/sc(S(N)(=O)=O)nn1C

InChI

InChI=1S/C5H8N4O3S2/c1-3(10)7-4-9(2)8-5(13-4)14(6,11)12/h1-2H3,(H2,6,11,12)/b7-4+

Molecular Formula

C5H8N4O3S2

HBD / HBA

1 / 6

Enlaces Rotables

1

Átomos Pesados

14

No targets recorded

Target interaction data is not yet available for this drug.

No interactions recorded

Drug interaction data is not yet available for this compound.

No side effects recorded

Side effect data is not yet available for this drug.

Preguntas frecuentes

A carbonic anhydrase inhibitor used to lower elevated intraocular (eye) pressure in people with glaucoma who cannot tolerate or do not respond adequately to other treatments. It helps prevent vision loss by reducing fluid buildup in the eye.

Selectively blocks angiotensin II type 1 (AT1) receptors, preventing the vasoconstrictive and aldosterone-secreting effects of angiotensin II. This results in vasodilation, reduced sodium retention, and decreased blood pressure.

Yes, Methazolamide is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.

{# References & Data Sources section for drug detail pages. Renders standard pharmacological database links plus the drug's data_sources field. #}

References & Data Sources

  • ChEMBL — European Bioinformatics Institute (EBI). CHEMBL19. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 4100. Chemical information database.

Data aggregated from publicly available pharmacological databases. Last updated 2026-03-28.

Aviso médico

This content is for educational and informational purposes only. It is not a substitute for professional medical advice, diagnosis, or treatment. Always consult a qualified healthcare provider before making medication decisions.

Data sources: ChEMBL, PubChem, DailyMed.