Etidronic Acid

CHEMBL871 Phase 4 承認済み Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
206.0 g/mol
LogP
-3.7
Phase
4

This bisphosphonate medication slows bone breakdown by inhibiting osteoclasts, the cells responsible for dissolving bone tissue. It is used to treat Paget's disease and to prevent bone loss in certain conditions.

分子量

206.0300 g/mol

LogP

-3.70

TPSA

135.00 Ų

リピンスキーの五則

適合

治療領域

作用機序

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)

機序

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.

2D構造

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SMILES

CC(O)(P(=O)(O)O)P(=O)(O)O

InChI

InChI=1S/C2H8O7P2/c1-2(3,10(4,5)6)11(7,8)9/h3H,1H3,(H2,4,5,6)(H2,7,8,9)

Molecular Formula

C2H8O7P2

HBD / HBA

5 / 7

回転可能結合数

2

重原子数

11

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.

よくある質問

This bisphosphonate medication slows bone breakdown by inhibiting osteoclasts, the cells responsible for dissolving bone tissue. It is used to treat Paget's disease and to prevent bone loss in certain conditions.

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, Etidronic Acid 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). CHEMBL871. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 3305. Chemical information database.

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

医学的免責事項

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.