Raloxifene
A selective estrogen receptor modulator used to prevent and treat osteoporosis in postmenopausal women and to reduce the risk of invasive breast cancer in women at high risk. It mimics some of estrogen's beneficial effects on bone density without stimulating breast or uterine tissue.
분자량
473.6000 g/mol
LogP
6.10
TPSA
98.20 Ų
리핀스키 5의 법칙
통과
치료 영역
Pharmacokinetics (PK)
Pharmacodynamics (PD)
2D 구조
Cite this structure
Embed this structure
SMILES
O=C(c1ccc(OCCN2CCCCC2)cc1)c1c(-c2ccc(O)cc2)sc2cc(O)ccc12
InChI
InChI=1S/C28H27NO4S/c30-21-8-4-20(5-9-21)28-26(24-13-10-22(31)18-25(24)34-28)27(32)19-6-11-23(12-7-19)33-17-16-29-14-2-1-3-15-29/h4-13,18,30-31H,1-3,14-17H2
Molecular Formula
C28H27NO4S
HBD / HBA
2 / 6
회전 가능 결합
7
무거운 원자
34
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
A selective estrogen receptor modulator used to prevent and treat osteoporosis in postmenopausal women and to reduce the risk of invasive breast cancer in women at high risk. It mimics some of estrogen's beneficial effects on bone density without stimulating breast or uterine tissue.
Yes, Raloxifene 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). CHEMBL81. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 5035. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-28.
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