Etidronate Disodium

CHEMBL1201042 Phase 4 ได้รับการอนุมัติ Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
250.0 g/mol
LogP
Phase
4

The disodium salt form of etidronic acid, this bisphosphonate slows the excessive bone turnover seen in Paget's disease of bone and helps maintain bone density to prevent fractures. It inhibits specialized bone-dissolving cells.

น้ำหนักโมเลกุล

249.9900 g/mol

TPSA

141.00 Ų

ด้านการรักษา

กลไกการออกฤทธิ์

Binds to hydroxyapatite crystals in bone, inhibiting osteoclast-mediated bone resorption by disrupting the mevalonate pathway within osteoclasts. This reduces bone turnover and increases bone mineral density.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

กลไก

Binds to hydroxyapatite crystals in bone, inhibiting osteoclast-mediated bone resorption by disrupting the mevalonate pathway within osteoclasts. This reduces bone turnover and increases bone mineral density.

โครงสร้าง 2 มิติ

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SMILES

CC(O)(P(=O)([O-])O)P(=O)([O-])O.[Na+].[Na+]

InChI

InChI=1S/C2H8O7P2.2Na/c1-2(3,10(4,5)6)11(7,8)9;;/h3H,1H3,(H2,4,5,6)(H2,7,8,9);;/q;2*+1/p-2

Molecular Formula

C2H6Na2O7P2

HBD / HBA

3 / 7

พันธะที่หมุนได้

2

อะตอมหนัก

13

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.

คำถามที่พบบ่อย

The disodium salt form of etidronic acid, this bisphosphonate slows the excessive bone turnover seen in Paget's disease of bone and helps maintain bone density to prevent fractures. It inhibits specialized bone-dissolving cells.

Binds to hydroxyapatite crystals in bone, inhibiting osteoclast-mediated bone resorption by disrupting the mevalonate pathway within osteoclasts. This reduces bone turnover and increases bone mineral density.

Yes, Etidronate Disodium 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). CHEMBL1201042. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 23894. Chemical information database.

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

ข้อจำกัดความรับผิดชอบทางการแพทย์

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.