Informations sur le produit
- 8,11-Epoxy-9,12-ethano-11,15-methano-11H-[1,8]dioxacycloheptadecino[4,3-b]pyridine-5,17-dione, 10,13,14,21,22-pentakis(acetyloxy)-12-[(acetyloxy)methyl]-7,8,9,10,12,13,14,15,18,19-decahydro-20-hydroxy-8,18,19,20-tetramethyl-, (8R,9R,10R,11S,12S,13R,14R,15S,18S,19S,20S,21S,22R)-
- (8R,9R,10R,11S,12S,13R,14R,15S,18S,19S,20S,21S,22R)-10,13,14,21,22-Pentakis(acetyloxy)-12-[(acetyloxy)methyl]-7,8,9,10,12,13,14,15,18,19-decahydro-20-hydroxy-8,18,19,20-tetramethyl-8,11-epoxy-9,12-ethano-11,15-methano-11H-[1,8]dioxacycloheptadecino[4,3-b]pyridine-5,17-dione
- Evonine, 8-(acetyloxy)-8-deoxo-, (8α)-
- 8,11-Epoxy-9,12-ethano-11,15-methano-11H-[1,8]dioxacycloheptadecino[4,3-b]pyridine-5,17-dione, 10,13,14,21,22-pentakis(acetyloxy)-12-[(acetyloxy)methyl]-7,8,9,10,12,13,14,15,18,19-decahydro-20-hydroxy-8,18,19,20-tetramethyl-, [8R-(8R*,9R*,10R*,11S*,12S*,13R*,14R*,15S*,18S*,19S*,20S*,21S*,22R*)]-
Euonymine is a sesquiterpene lactone that has been found to possess anticancer activity. It is derived from the Chinese medicine preparation, Tripterygium wilfordii Hook.f (TWH), and is structurally similar to acanthothamine. Euonymine has been shown to inhibit cancer cell proliferation and tumor growth in mice. This compound also exhibits anticancer activity against human prostate cancer cells in vitro by inhibiting DNA synthesis and protein synthesis, as well as inducing apoptosis of cancer cells.