Inhibitors for protein-protein interactions are challenging to design, in part due to the unique and complex architectures of each protein's interaction domain. Most approaches to develop inhibitors for these interactions rely on rational design, which requires prior structural knowledge of the targ
Combinatorial modification of 2-ketopiperazine with solid phase C-alkylation and N-acylations
✍ Scribed by Zhaoning Zhu; Brian Mckittrick
- Publisher
- Elsevier Science
- Year
- 1998
- Tongue
- French
- Weight
- 181 KB
- Volume
- 39
- Category
- Article
- ISSN
- 0040-4039
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