Alendronate Sodium
The sodium salt form of alendronic acid, a bisphosphonate medication that prevents bone breakdown by inhibiting osteoclast cells responsible for bone resorption. It is widely used to treat and prevent osteoporosis in postmenopausal women and men, and to treat Paget's disease of bone, significantly reducing the risk of fractures.
分子量
325.1200 g/mol
TPSA
167.00 Ų
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)
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
Cite this structure
Embed this structure
SMILES
NCCCC(O)(P(=O)([O-])O)P(=O)(O)O.[Na+]
InChI
InChI=1S/C4H13NO7P2.Na/c5-3-1-2-4(6,13(7,8)9)14(10,11)12;/h6H,1-3,5H2,(H2,7,8,9)(H2,10,11,12);/q;+1/p-1
Molecular Formula
C4H18NNaO10P2
HBD / HBA
8 / 11
回転可能結合数
5
重原子数
18
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
The sodium salt form of alendronic acid, a bisphosphonate medication that prevents bone breakdown by inhibiting osteoclast cells responsible for bone resorption. It is widely used to treat and prevent osteoporosis in postmenopausal women and men, and to treat Paget's disease of bone, significantly reducing the risk of fractures.
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, Alendronate Sodium is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.
References & Data Sources
- ChEMBL — European Bioinformatics Institute (EBI). CHEMBL675. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 23681107. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.
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