2010 Fiscal Year Final Research Report
Diversity-oriented synthesis of natural product analogs and development of lead candidates for anti-infectious agents
| Project/Area Number |
19681022
|
|---|
| Research Category |
Grant-in-Aid for Young Scientists (A)
|
| Allocation Type | Single-year Grants |
|---|
| Research Field |
Living organism molecular science
|
|---|
| Research Institution | Hokkaido University |
|---|
Principal Investigator |
OGURI Hiroki Hokkaido University, 大学院・理学研究院, 准教授 (80311546)
|
|---|
| Project Period (FY) |
2007 – 2010
|
| Keywords | 生理活性分子の設計・合成 |
|---|
| Research Abstract |
To access high-quality small molecule libraries to screen lead candidates for neglected diseases exemplified by human African trypanosomiasis, we sought to develop a synthetic process that would produce collections of cyclic scaffolds relevant to an assortment of natural products exhibiting desirable biological activities. By extracting the common structural features among several sesquiterpenes including artemisinin, anthecularin and transtaganolides, we designed six types of scaffolds with systematic structural variations consisting of (i) three types of stereochemical relationships on the sp^3 ring-junctions and (ii) two distinct arrays of tricyclic frameworks. Amodular and stereo-divergent assembly of dienynes exploiting a versatile manifold produced a series of cyclization precursors. Divergent cyclizations of the dienynes employing tandem ring-closing metathesis reactions overrode variant reactivities of the cyclization precursors leading to the six canonical sets of the tricyclic scaffolds incorporating a diene group. Screenings of trypanosomal activities of the canonical sets, as well as regio- and stereoisomers of the tricyclic dienes, allowed generation of several anti-trypanosomal agents defining the three-dimensional shape of the pharmacophore. The candidate tricyclic dienes were selected by primary screenings and further subjected to installation of a peroxide bridge, which generated artemisinin analogs that exhibited potent in vitro anti-trypanosomal activities comparable or even superior to those of artemisinin and approved drugs, suramin and eflornithine.
|
-
[Journal Article] Generation of anti-trypanosomal agents through concise synthesis and structural diversification of sesquiterpene analogs2011
Author(s)
Oguri, H., Hiruma, T., Yamagishi, Y., Oikawa, H., Ishiyama, A., Otoguro, K., Yamada, H., Omura, S.
-
Journal Title
J.Am.Chem.Soc. Selected for the Front Cover. 133
Pages: 7096-7105
Peer Reviewed
-
-
-
-
-
-
-
-
-
-
