Design, synthesis and CoMFA studies of N1-amino acid substituted 2,4,5-triphenyl imidazoline derivatives as p53-MDM2 binding inhibitors. [electronic resource]
Producer: 20120618Description: 1417-24 p. digitalISSN:- 1464-3391
- Animals
- Antineoplastic Agents -- chemical synthesis
- Cell Line, Tumor
- Drug Design
- Humans
- Imidazoles -- chemistry
- Imidazolines -- chemical synthesis
- Inhibitory Concentration 50
- Models, Biological
- Molecular Structure
- Piperazines -- chemistry
- Protein Binding -- drug effects
- Proto-Oncogene Proteins c-mdm2 -- antagonists & inhibitors
No physical items for this record
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
There are no comments on this title.
Log in to your account to post a comment.