Strontium Ranelate

CHEMBL3707306 Phase 4 Disetujui 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.

Berat Molekul

513,5000 g/mol

TPSA

216,00 Ų

Area Terapeutik

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Struktur 2D

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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

Ikatan yang Dapat Dirotasi

4

Atom Berat

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.

Pertanyaan yang Sering Diajukan

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.

Penyangkalan Medis

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.