Rational Design of Small Molecules Modulating Protein-Protein Interaction
| Project/Area Number |
20790097
|
|---|
| Research Category |
Grant-in-Aid for Young Scientists (B)
|
| Allocation Type | Single-year Grants |
|---|
| Research Field |
Drug development chemistry
|
|---|
| Research Institution | Hokkaido University |
|---|
Principal Investigator |
ICHIKAWA Satoshi Hokkaido University, 大学院・薬学研究院, 准教授 (60333621)
|
|---|
| Project Period (FY) |
2008 – 2009
|
| Project Status |
Completed (Fiscal Year 2009)
|
| Budget Amount *help |
¥4,290,000 (Direct Cost: ¥3,300,000、Indirect Cost: ¥990,000)
Fiscal Year 2009: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
Fiscal Year 2008: ¥2,600,000 (Direct Cost: ¥2,000,000、Indirect Cost: ¥600,000)
|
|---|
| Keywords | タンパク質間相互作用 / C-リボシル化反応 / 有機合成 / C-アリル化反応 |
|---|
| Research Abstract |
This study is to develop a stereoselective C-glycosylation reaction to give C-glycosides, which can be a key intermediate of oxabicyclo[n,2.1]system designed as a scaffold of small molecule protein-protein interaction inhibitors. Reactions of 2,3-O-(3-pentylidene)-D-ribofuranosyl fluoride with various allyltrimethylsilane derivatives exhibited excellent β-selectivity providing a range of β-C-allylribosides (β/α=>98/2). This strategy will provide a new concept to synthesize β-C-allylribosides, which are biologically relevant molecules such as small molecule protein-protein interaction inhibitors, by controlling the effect of steric hindrance in the transition state.
|
Report
(3 results)
Research Products
(45 results)
