Synthesis, chiral resolution, and determination of novel furan lignan derivatives with potent anti-tumor activity
Two chiral furan lignan was synthesized, chiral separated and their absolute configuration was determined by circular dichroism spectra. Compound 2c (IC 50 = 12 μM on QGY-7701), the racemate of 2a and 2b, is reported. A kind of racemic furan lignans were synthesized via a novel route, and two optica...
Gespeichert in:
Veröffentlicht in: | Bioorganic & medicinal chemistry letters 2010-03, Vol.20 (6), p.1961-1964 |
---|---|
Hauptverfasser: | , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | Two chiral furan lignan was synthesized, chiral separated and their absolute configuration was determined by circular dichroism spectra. Compound
2c (IC
50
=
12
μM on QGY-7701), the racemate of
2a and
2b, is reported.
A kind of racemic furan lignans were synthesized via a novel route, and two optical isomers were obtained through a selective hydrolization. The absolute configurations were determined by circular dichroism spectroscopy after separated through a preparative column. The different activities of isomers and the racemates were evaluated on QGY-7701 and HeLa cell lines, and compound
2c showed the best activity on QGY-7701 and HeLa cell lines with IC
50 12
μM and 13
μM, respectively. |
---|---|
ISSN: | 0960-894X 1464-3405 |
DOI: | 10.1016/j.bmcl.2010.01.122 |