Strontium Ranelate

CHEMBL3707306 Phase 4 承認済み Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
513.5 g/mol
LogP
Phase
4

Strontium ranelate is a dual-action bone agent used for the treatment of osteoporosis, combining the actions of both inhibiting osteoclast-mediated bone resorption and stimulating osteoblast-mediated bone formation by interacting with the calcium-sensing receptor. By simultaneously reducing bone breakdown and promoting bone synthesis, it improves bone microarchitecture and reduces fracture risk at both vertebral and non-vertebral sites. It has been restricted in some markets due to cardiovascular and venous thromboembolic risks.

分子量

513.5000 g/mol

TPSA

216.00 Ų

治療領域

Pharmacokinetics (PK)

Pharmacodynamics (PD)

2D構造

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SMILES

N#Cc1c(N(CC(=O)[O-])CC(=O)[O-])sc(C(=O)[O-])c1CC(=O)[O-].[Sr+2].[Sr+2]

InChI

InChI=1S/C12H10N2O8S.2Sr/c13-2-6-5(1-7(15)16)10(12(21)22)23-11(6)14(3-8(17)18)4-9(19)20;;/h1,3-4H2,(H,15,16)(H,17,18)(H,19,20)(H,21,22);;/q;2*+2/p-4

Molecular Formula

C12H6N2O8SSr2

HBD / HBA

- / 11

回転可能結合数

4

重原子数

25

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

Strontium ranelate is a dual-action bone agent used for the treatment of osteoporosis, combining the actions of both inhibiting osteoclast-mediated bone resorption and stimulating osteoblast-mediated bone formation by interacting with the calcium-sensing receptor. By simultaneously reducing bone breakdown and promoting bone synthesis, it improves bone microarchitecture and reduces fracture risk at both vertebral and non-vertebral sites. It has been restricted in some markets due to cardiovascular and venous thromboembolic risks.

Yes, Strontium Ranelate 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). CHEMBL3707306. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 6918182. Chemical information database.

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

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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.