Bithionolate Sodium

CHEMBL1447476 Phase 4 Đã phê duyệt Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
400.0 g/mol
LogP
Phase
4

The sodium salt form of bithionol, an older antiparasitic agent used historically against fascioliasis and other parasitic infections. Like bithionol, it has largely been replaced by safer and more effective antiparasitic drugs. It is considered largely obsolete in modern medicine.

Khối lượng phân tử

400,0000 g/mol

TPSA

71,40 Ų

Cơ chế tác dụng

Disrupts essential metabolic pathways or structural components of parasitic organisms, leading to paralysis, starvation, or death of the parasite.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Cơ chế

Disrupts essential metabolic pathways or structural components of parasitic organisms, leading to paralysis, starvation, or death of the parasite.

Cấu trúc 2D

SVG PNG

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SMILES

[Na+].[Na+].[O-]c1c(Cl)cc(Cl)cc1Sc1cc(Cl)cc(Cl)c1[O-]

InChI

InChI=1S/C12H6Cl4O2S.2Na/c13-5-1-7(15)11(17)9(3-5)19-10-4-6(14)2-8(16)12(10)18;;/h1-4,17-18H;;/q;2*+1/p-2

Molecular Formula

C12H4Cl4Na2O2S

HBD / HBA

- / 3

Liên kết có thể quay

2

Nguyên tử nặng

21

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

The sodium salt form of bithionol, an older antiparasitic agent used historically against fascioliasis and other parasitic infections. Like bithionol, it has largely been replaced by safer and more effective antiparasitic drugs. It is considered largely obsolete in modern medicine.

Disrupts essential metabolic pathways or structural components of parasitic organisms, leading to paralysis, starvation, or death of the parasite.

Yes, Bithionolate Sodium 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). CHEMBL1447476. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 22882. 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.