Abstract:Three 18(4→3)-abeo-abietanoids, a new natural product and two new compounds, named tripordolides A–C (1–3), were isolated from the leaves of Tripterygium wilfordii. Their structures were elucidated on the basis of their spectroscopic analysis, and the absolute configuration of compounds was confirmed by CD and X-ray crystallographic analysis using anomalous scattering of Cu Kα radiation. Compounds 1 and 3 showed moderate inhibitory activities against NO production in lipopolysaccharide-induced (LPS) RAW 264.7 … Show more
“…Previously unknown tripordolide C was isolated from the leaves of Tripterygium wilfordii . 126 Tripordolide C was evaluated for its in vitro inhibitory activities against NO production in lipopolysaccharide-induced RAW 264.7 macrophages. Tripordolide C showed moderate inhibition of NO production in mouse peritoneal macrophage at a concentration of 10 μM.…”
Section: Epoxyhydroquinonesmentioning
confidence: 99%
“…Previously unknown tripordolide C was isolated from the leaves of Tripterygium wilfordii. 126 Tripordolide C was evaluated for its in vitro inhibitory activities against NO production in lipopolysaccharide-induced RAW 264.7 macrophages.…”
This review provides an updated outlook on the isolation of epoxyquinoids and an examination of their biological profile. Total, enantioselective synthesis, and the development of shorter approaches to construction of epoxyquinoids are addressed.
“…Previously unknown tripordolide C was isolated from the leaves of Tripterygium wilfordii . 126 Tripordolide C was evaluated for its in vitro inhibitory activities against NO production in lipopolysaccharide-induced RAW 264.7 macrophages. Tripordolide C showed moderate inhibition of NO production in mouse peritoneal macrophage at a concentration of 10 μM.…”
Section: Epoxyhydroquinonesmentioning
confidence: 99%
“…Previously unknown tripordolide C was isolated from the leaves of Tripterygium wilfordii. 126 Tripordolide C was evaluated for its in vitro inhibitory activities against NO production in lipopolysaccharide-induced RAW 264.7 macrophages.…”
This review provides an updated outlook on the isolation of epoxyquinoids and an examination of their biological profile. Total, enantioselective synthesis, and the development of shorter approaches to construction of epoxyquinoids are addressed.
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