Trichlormethiazide

CHEMBL1054 Phase 4 Aprovado Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
380.7 g/mol
LogP
0.6
Phase
4

Trichlormethiazide is a thiazide diuretic that inhibits the sodium-chloride symporter (NCC) in the distal convoluted tubule, reducing sodium and chloride reabsorption and increasing urinary excretion of sodium, chloride, potassium, and water. It is used for the treatment of hypertension and edematous conditions including congestive heart failure and renal disease, lowering blood pressure through initial volume reduction and later through peripheral vasodilation. Like other thiazides, it can cause hypokalemia, hyponatremia, and hyperuricemia as metabolic adverse effects.

Peso Molecular

380,7000 g/mol

LogP

0,60

TPSA

135,00 Ų

Regra dos 5 de Lipinski

Aprovado

Áreas Terapêuticas

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Estrutura 2D

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SMILES

NS(=O)(=O)c1cc2c(cc1Cl)NC(C(Cl)Cl)NS2(=O)=O

InChI

InChI=1S/C8H8Cl3N3O4S2/c9-3-1-4-6(2-5(3)19(12,15)16)20(17,18)14-8(13-4)7(10)11/h1-2,7-8,13-14H,(H2,12,15,16)

Molecular Formula

C8H8Cl3N3O4S2

HBD / HBA

3 / 7

Ligações Rotacionáveis

2

Átomos Pesados

20

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.

Perguntas frequentes

Trichlormethiazide is a thiazide diuretic that inhibits the sodium-chloride symporter (NCC) in the distal convoluted tubule, reducing sodium and chloride reabsorption and increasing urinary excretion of sodium, chloride, potassium, and water. It is used for the treatment of hypertension and edematous conditions including congestive heart failure and renal disease, lowering blood pressure through initial volume reduction and later through peripheral vasodilation. Like other thiazides, it can cause hypokalemia, hyponatremia, and hyperuricemia as metabolic adverse effects.

Yes, Trichlormethiazide 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). CHEMBL1054. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 5560. 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.