Minodronic Acid

CHEMBL319144 Phase 4 승인됨 Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
322.2 g/mol
LogP
-2.2
Phase
4

This bisphosphonate medication is used in Japan to treat osteoporosis by inhibiting osteoclast activity, the cells responsible for breaking down bone, thereby slowing bone loss and reducing fracture risk. Like other bisphosphonates, it is taken orally and builds up preferentially in bone tissue.

분자량

322.1500 g/mol

LogP

-2.20

TPSA

153.00 Ų

리핀스키 5의 법칙

통과

치료 영역

작용 기전

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)

기전

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 구조

SVG PNG

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SMILES

O=P(O)(O)C(O)(Cc1cnc2ccccn12)P(=O)(O)O

InChI

InChI=1S/C9H12N2O7P2/c12-9(19(13,14)15,20(16,17)18)5-7-6-10-8-3-1-2-4-11(7)8/h1-4,6,12H,5H2,(H2,13,14,15)(H2,16,17,18)

Molecular Formula

C9H12N2O7P2

HBD / HBA

5 / 8

회전 가능 결합

4

무거운 원자

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.

자주 묻는 질문

This bisphosphonate medication is used in Japan to treat osteoporosis by inhibiting osteoclast activity, the cells responsible for breaking down bone, thereby slowing bone loss and reducing fracture risk. Like other bisphosphonates, it is taken orally and builds up preferentially in bone tissue.

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, Minodronic 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). CHEMBL319144. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 130956. Chemical information database.

Data aggregated from publicly available pharmacological databases. Last updated 2026-03-28.

의학적 면책조항

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.