Bazedoxifene
A selective estrogen receptor modulator that acts as an estrogen antagonist in breast and uterine tissue while providing estrogen-like protection to bone, used to prevent postmenopausal osteoporosis.
Molecular Weight
470.6000 g/mol
LogP
6.10
TPSA
57.90 Ų
Lipinski RO5
Pass
Therapeutic Areas
Pharmacokinetics (PK)
Pharmacodynamics (PD)
2D Structure
Cite this structure
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SMILES
Cc1c(-c2ccc(O)cc2)n(Cc2ccc(OCCN3CCCCCC3)cc2)c2ccc(O)cc12
InChI
InChI=1S/C30H34N2O3/c1-22-28-20-26(34)12-15-29(28)32(30(22)24-8-10-25(33)11-9-24)21-23-6-13-27(14-7-23)35-19-18-31-16-4-2-3-5-17-31/h6-15,20,33-34H,2-5,16-19,21H2,1H3
Molecular Formula
C30H34N2O3
HBD / HBA
2 / 4
Rotatable Bonds
7
Heavy Atoms
35
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.
Frequently Asked Questions
A selective estrogen receptor modulator that acts as an estrogen antagonist in breast and uterine tissue while providing estrogen-like protection to bone, used to prevent postmenopausal osteoporosis.
Yes, Bazedoxifene 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). CHEMBL46740. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 154257. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.
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