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Estrogen receptor ligands. Part 6: Synthesis and binding affinity of dihydrobenzodithiins
- Source :
- Bioorganic & Medicinal Chemistry Letters. 14:3753-3755
- Publication Year :
- 2004
- Publisher :
- Elsevier BV, 2004.
-
Abstract
- Dihydrobenzodithiin compounds (1-6) were prepared to explore the expansion of the dihydrobenzoxathiin lead compounds I-III as SERAMs (Selective Estrogen Receptor Alpha Modulators). The dihydrobenzodithiin compounds generally maintained a high degree of selectivity for ERalpha over ERbeta, however, they lacked the in vivo antagonism/agonism activity exhibited by the lead class in an immature rat uterine growth model.
- Subjects :
- Selective Estrogen Receptor Modulators
Agonist
medicine.drug_class
Clinical Biochemistry
Pharmaceutical Science
Estrogen receptor
Ligands
Heterocyclic Compounds, 2-Ring
Models, Biological
Biochemistry
Inhibitory Concentration 50
Structure-Activity Relationship
Piperidines
Drug Discovery
medicine
Animals
Estrogen Receptor beta
Structure–activity relationship
Binding site
Receptor
Molecular Biology
Cells, Cultured
Estrogen receptor beta
Binding Sites
Chemistry
Uterus
Organic Chemistry
Estrogen Receptor alpha
Rats
Receptors, Estrogen
Selective estrogen receptor modulator
Molecular Medicine
Female
Estrogen receptor alpha
hormones, hormone substitutes, and hormone antagonists
Subjects
Details
- ISSN :
- 0960894X
- Volume :
- 14
- Database :
- OpenAIRE
- Journal :
- Bioorganic & Medicinal Chemistry Letters
- Accession number :
- edsair.doi.dedup.....09fe34d29848f4b92d65cc5c353a737f
- Full Text :
- https://doi.org/10.1016/j.bmcl.2004.04.101