Sie befinden Sich nicht im Netzwerk der Universität Paderborn. Der Zugriff auf elektronische Ressourcen ist gegebenenfalls nur via VPN oder Shibboleth (DFN-AAI) möglich. mehr Informationen...
Bioorganic & medicinal chemistry letters, 2014-05, Vol.24 (9), p.2202-2205
2014

Details

Autor(en) / Beteiligte
Titel
Synthesis and cytotoxic activity of nitric oxide-releasing isosteviol derivatives
Ist Teil von
  • Bioorganic & medicinal chemistry letters, 2014-05, Vol.24 (9), p.2202-2205
Ort / Verlag
England: Elsevier Ltd
Erscheinungsjahr
2014
Link zum Volltext
Quelle
MEDLINE
Beschreibungen/Notizen
  • Fifteen novel hybrids containing diterpene skeleton and nitric oxide (NO) donor were prepared from isosteviol. All the compounds were tested on preliminary cytotoxicity, and the results showed that six target compounds (8c, 10b, 14a, 14c, 18c, and 18d) exhibited anti-proliferation activity on HepG2 cells, with 8c (IC50=4.24μM) and 18d (IC50=2.75μM) superior to the positive control CDDO-Me (2-cyano-3,12-dioxooleana-1,9(11)-dien-28-acid methyl ester, IC50=4.99μM); eleven target compounds (8a–c, 9a–c, 10a–b, 14a, 14c, 18d) exhibited anti-proliferation activities on B16F10 cells at different levels, among them, seven compounds were more potent than comptothecin (IC50=2.78μM) and CDDO-Me (IC50=5.85μM), particularly, 10b (IC50=0.02μM) presented the strongest effect, which was selected as a candidate for further study.

Weiterführende Literatur

Empfehlungen zum selben Thema automatisch vorgeschlagen von bX