Benzthiazide

CHEMBL1201039 Phase 4 Đã phê duyệt Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
431.9 g/mol
LogP
1.7
Phase
4

A thiazide-type diuretic that was used to treat high blood pressure and fluid retention by increasing urine output. It works in the kidneys to promote the excretion of sodium and water. It has largely been replaced by other thiazide diuretics in current practice.

Khối lượng phân tử

431,9000 g/mol

LogP

1,70

TPSA

161,00 Ų

Lipinski RO5

Đạt

Cơ chế tác dụng

Inhibits sodium reabsorption in the renal tubules, promoting excretion of sodium, chloride, and water. This reduces extracellular fluid volume and cardiac preload, lowering blood pressure.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Cơ chế

Inhibits sodium reabsorption in the renal tubules, promoting excretion of sodium, chloride, and water. This reduces extracellular fluid volume and cardiac preload, lowering blood pressure.

Cấu trúc 2D

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SMILES

NS(=O)(=O)c1cc2c(cc1Cl)N=C(CSCc1ccccc1)NS2(=O)=O

InChI

InChI=1S/C15H14ClN3O4S3/c16-11-6-12-14(7-13(11)25(17,20)21)26(22,23)19-15(18-12)9-24-8-10-4-2-1-3-5-10/h1-7H,8-9H2,(H,18,19)(H2,17,20,21)

Molecular Formula

C15H14ClN3O4S3

HBD / HBA

2 / 7

Liên kết có thể quay

5

Nguyên tử nặng

26

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.

Câu hỏi thường gặp

A thiazide-type diuretic that was used to treat high blood pressure and fluid retention by increasing urine output. It works in the kidneys to promote the excretion of sodium and water. It has largely been replaced by other thiazide diuretics in current practice.

Inhibits sodium reabsorption in the renal tubules, promoting excretion of sodium, chloride, and water. This reduces extracellular fluid volume and cardiac preload, lowering blood pressure.

Yes, Benzthiazide 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). CHEMBL1201039. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 2343. Chemical information database.

Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.

Tuyên bố miễn trách y tế

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.