Isoimperatorin

製品コードS3904 バッチS390401

印刷

化学情報

 Chemical Structure Synonyms N/A Storage
(From the date of receipt)
3 years -20°C powder
1 years -80°C in solvent
化学式

C16H14O4

分子量 270.28 CAS No. 482-45-1
Solubility (25°C)* 体外 DMSO 54 mg/mL (199.79 mM)
* <1 mg/ml means slightly soluble or insoluble.
* Please note that Selleck tests the solubility of all compounds in-house, and the actual solubility may differ slightly from published values. This is normal and is due to slight batch-to-batch variations.

溶剤液(一定の濃度)を調合する

生物活性

製品説明 Isoimperatorin, a natural furanocoumarin that can be isolated from a variety of plant parts, has analgesic, antimicrobial, vascular relaxing and anticancer activities.
in vitro

Isoimperatorin significantly inhibits the proliferation of SGC-7901 cells in a dose- and time-dependent manner, and the half maximal inhibitory concentration is 18.75 µg/ml. The expression levels of the pro-apoptotic proteins, Bax, c-caspase-3 and c-caspase-9, are significantly increased and the expression levels of the anti-apoptotic proteins, Survivin and Bcl-2, are significantly reduced after the treatment[1].

in vivo

Isoimperatorin significantly inhibits the growth of SGC-7901 cell-induced tumor in vivo by increasing the expression levels of pro-apoptotic proteins (Bax, c-caspase-3 and c-caspase-9) and reducing the expression levels of anti-apoptotic proteins (Survivin and Bcl-2) without adverse effects on the increasing body weight of nude mice[1].

プロトコル(参考用のみ)

細胞アッセイ 細胞株 SGC-7901 cells
濃度 5, 10, 15, 20, 25, 30, 35 and 40 µg/ml
反応時間 48 h
実験の流れ

The antiproliferative activity of isoimperatorin against SGC-7901 cells was evaluated using an MTT reduction assay. The SGC-7901 cells were seeded on 96-well culture plates with RPMI-1640 medium at a density of 5×103 cells/well. After 24 h of incubation at 37°C in 5% CO2/95% air, the cells were treated at different concentrations of isoimperatorin (5, 10, 15, 20, 25, 30, 35 and 40 µg/ml) and 0.05% DMSO (control) for 48 h to examine dose-dependency; or with isoimperatorin at a concentration of 20 µg/ml and 0.05% DMSO (control) for 12, 24, 36, 48, 60 and 72 h to examine time-dependent effects. Subsequently, 20 µl MTT (5 mg/ml) was separately added into each well, and the cells were cultured at 37°C in 5% CO2/95% air for another 3 h. Subsequently, 200 µl DMSO was separately added into each well and the optical density (OD) of the DMSO solution was measured at 570 nm using a microplate reader.

動物実験 動物モデル Sixteen female nude mice (5–6 weeks old) inoculated with SGC-7901 cells (tumor xenograft model)
投薬量 10 mg/kg
投与方法 i.p.

長期の保管のために-20°Cの下で製品を保ってください。

人間や獣医の診断であるか治療的な使用のためにでない。

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