Powder: -20°C for 3 years
In solvent: -80°C for 2 years
Dehydroglyasperin D exhibits anticancer, anti-inflammatory, anti-obesity, antioxidant and anti-aldose reductase effects, it inhibits the proliferation of HT-29 human colorectal cancer cells through direct interaction with phosphatidylinositol 3-kinase; it also mediates suppression of both COX-2 expression and the MLK3 signalling pathway through direct binding and inhibition of MLK3. Dehydroglyasperin D shows strong ferric reducing activities and effectively scavenged DPPH, ABTS(+), and singlet oxygen radicals.
Description | Dehydroglyasperin D exhibits anticancer, anti-inflammatory, anti-obesity, antioxidant and anti-aldose reductase effects, it inhibits the proliferation of HT-29 human colorectal cancer cells through direct interaction with phosphatidylinositol 3-kinase; it also mediates suppression of both COX-2 expression and the MLK3 signalling pathway through direct binding and inhibition of MLK3. Dehydroglyasperin D shows strong ferric reducing activities and effectively scavenged DPPH, ABTS(+), and singlet oxygen radicals. |
Molecular Weight | 368.42 |
Formula | C22H24O5 |
CAS No. | 517885-72-2 |
Powder: -20°C for 3 years
In solvent: -80°C for 2 years
( < 1 mg/ml refers to the product slightly soluble or insoluble )
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Dehydroglyasperin D 517885-72-2 DNA损伤和修复 G蛋白偶联受体 MAPK信号通路 PI3K/Akt/mTOR信号通路 干细胞 免疫与炎症 神经科学 细胞骨架 细胞周期 p38 MAPK PI3K Prostaglandin Receptor ROS COX DNA/RNA Synthesis Akt GSK-3 JNK Inhibitor inhibitor inhibit