Structure of FD-895 Revealed through Total Synthesis
作者:Reymundo Villa、Alexander L. Mandel、Brian D. Jones、James J. La Clair、Michael D. Burkart
DOI:10.1021/ol3023006
日期:2012.11.2
The totalsynthesis of FD-895 was completed through a strategy that featured the use of a tandem esterification ring-closing metathesis (RCM) process to construct the 12-membered macrolide and a modified Stille coupling to append the side chain. These studies combined with detailed analysis of all four possible C16–C17 stereoisomers were used to confirm the structure of FD-895 and identify an analog
[EN] ANTI-CANCER POLYKETIDE COMPOUNDS<br/>[FR] COMPOSÉS DE POLYCÉTIDES ANTICANCÉREUX
申请人:UNIV CALIFORNIA
公开号:WO2013148324A1
公开(公告)日:2013-10-03
Provided herein, inter alia, are anticancer polyketides. The uses of the polyketides described herein include treatment of cancer, for example, through regulation of the spliceosome and detection of spliceosome inhibition.
Provided herein, inter alia, are anticancer polyketides. The uses of the polyketides described herein include treatment of cancer, for example, through regulation of the spliceosome and detection of spliceosome inhibition.
Provided herein, inter alia, are splice modulator compounds. The compounds include optically pure, stereospecific analogs of FD-895. The methods provided herein allow, for example, for scalable preparation of said compounds, and further allow, for example, use of said compounds for inhibiting spliceosome activity.