Parallel synthesis and SAR study of novel oxa-steroids as potent and selective progesterone receptor antagonists. [electronic resource]
Producer: 20070724Description: 2531-4 p. digitalISSN:- 0960-894X
- Animals
- Cell Line, Tumor
- Chemistry, Pharmaceutical -- methods
- Complement C3 -- metabolism
- Drug Design
- Female
- Humans
- Mifepristone -- pharmacology
- Models, Chemical
- Protein Binding
- Rats
- Receptors, Glucocorticoid -- antagonists & inhibitors
- Receptors, Progesterone -- antagonists & inhibitors
- Steroids -- chemistry
- Structure-Activity Relationship
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Publication Type: Journal Article
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