VK3-OCH3 是一种有效的抗肿瘤剂。 VK3-OCH3 对神经母细胞瘤细胞系显示细胞毒性，对正常细胞系显示低细胞毒性。 VK3-OCH3 在 IMR-32 细胞的 G2/M 期诱导细胞凋亡和细胞周期停滞。 VK3-OCH3 显示出抗肿瘤活性。
| Cas No. | 255906-59-3 |
| Canonical SMILES | O=C1C(SCCOC)=C(C)C(C2=CC=CC=C21)=O |
| 分子式 | C14H14O3S |
| 分子量 | 262.3 |
| 溶解度 | DMF: 30 mg/ml,DMF:PBS(pH 7.2)(1:1): 0.5 mg/ml,DMSO: 25 mg/ml,Ethanol: 5 mg/ml |
| 储存条件 | Store at -20°C |
| General tips | For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while. |
| Shipping Condition | Evaluation sample solution : ship with blue ice
All other available size: ship with RT , or blue ice upon request |
| 产品描述 | VK3-OCH3 is an analog of vitamin K3 that that has antiproliferative activities in vitro. It preferentially decreases proliferation of IMR-32, LA-N-1, NB-39, and SK-N-SH neuroblastoma cells (IC50s = 2.43, 1.55, 10.69, and 3.45 µM, respectively) compared with non-cancerous HUVEC and HDF cells (IC50s = 26.24 and 87.11 µM, respectively). It increases heme oxygenase-1 (HO-1) and caveolin-1 levels, induces apoptosis, and halts the cell cycle at the G2/M phase in IMR-32 cells. VK3-OCH3 also inhibits protein-tyrosine phosphorylase (PTPase) activity (IC50 = 57.2 µM in a cell-free assay), induces protein-tyrosine phosphorylation in Hep3B hepatoma cells when used at a concentration of 50 µM, and inhibits the growth of Hep3B cells (IC50 = 8.6 µM). |
m.cnreagent.com