Catalog No.S2382 Synonyms: Isoevodiamine
Molecular Weight(MW): 303.36
Evodiamine (Isoevodiamine), an alkaloid extract from the fruit of Evodiae Fructus exhibits antitumor activities against the human tumor cells. It is shown to inhibit NF-kB activation through suppression of IkB kinase activity.
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Evodiamine ameliorates PDGF‑BB‑induced oxidative stress in VSMCs. VSMCs were pretreated with 0.1 or 0.5 μM evodiamine for 24 h, and then stimulated with 10 ng/ml PDGF‑BB for 1 h. (A) ROS detection using 2' 7' dichlorofluorescin diacetate staining. Magnification, x200. (B) Quantitative data of five independent experiments, expressed as the fold increase, compared with the control. (C‑F) mRNA expression levels of antioxidant genes were assessed using reverse transcription‑quantitative polymerase chain reaction analysis. Data are presented as the mean+ standard deviation of three independent experiments. *P<0.05 and **P<0.01, compared with the control group; ##P<0.01, compared with the PDGF‑BB‑stimulated group. Evo, evodiamine; PDGF‑BB, platelet‑derived growth factor‑BB; VSMCs, vascular smooth muscle cells; ROS, reactive oxygen species; HO‑1, heme oxygenase‑1; GPx‑1, glutathione peroxidase 1; SOD, superoxide dismutase.
Mol Med Rep, 2016, 14(5):4551-4558.. Evodiamine purchased from Selleck.
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|Description||Evodiamine (Isoevodiamine), an alkaloid extract from the fruit of Evodiae Fructus exhibits antitumor activities against the human tumor cells. It is shown to inhibit NF-kB activation through suppression of IkB kinase activity.|
Evodiamine (Isoevodiamine), an alkaloid extract from Evodiae Fructus exhibits antitumor activities against the human tumor cells. Evodiamine induces the substantial amount of apoptosis both in Bcl-2- and Akt-overexpressing U937 cells but not in human peripheral blood mononuclear cells via caspase-independent apoptotic pathways.  Evodiamine Evodiamine also inhibits tumor necrosis factor (TNF)-induced NF-kappaB and Akt activation but it has no effect on JNK or p38 MAPK activation.  In addition, Evodiamine is an human topoisomerase I inhibitor. 
|In vivo||LD50: Mice 77mg/kg (i.v.) |
|In vitro||DMSO||<1 mg/mL|
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