| 产品描述: | Diethylmaleate is a glutathione-depleting compound that has been shown to induce apoptosis. Reports indicate that Diethylmaleate inhibits NF κ B activation, activates PDAP1 (Pap1), and modifies the endoribonuclease action of 26S proteasomes. Diethylmaleate is an activator of GHS-R1α.;Diethylmaleate is a glutathione-depleting compound that has been shown to induce apoptosis. Reports indicate that Diethylmaleate inhibits NF κ B activation, activates PDAP1 (Pap1), and modifies the endoribonuclease action of 26S proteasomes. Diethylmaleate is an activator of GHS-R1α.A glutathione-depleting compound that inhibits NF kappa B. |
| 体内研究: |
Diethyl maleate (4.6 mmol/kg;腹腔注射;单次;2 h) 使 Sprague-Dawley 大鼠肺/脑组织谷胱甘肽 (GSH) 减少 82%/45%,并缩短高压氧暴露下的惊厥/死亡时间。 Diethyl maleate (4.6 mmol/kg;腹腔注射;单次;24 h)在组织 GSH 水平恢复后不增强高氧毒性。Diethyl maleate (4.6 mmol/kg;腹腔注射;单次 + 90 分钟后补充等摩尔 GSH)逆转 GSH 耗竭并恢复高氧暴露大鼠存活时间。 |
| 参考文献: |
1. Andrea Gille, et al. Nuclear trapping of inactive FOXO1 by the Nrf2 activator diethyl maleate. Redox Biol. 2019 Jan;20:19-27. 2. Weber CA, et al. Depletion of tissue glutathione with diethyl maleate enhances hyperbaric oxygen toxicity. Am J Physiol. 1990 Jun;258(6 Pt 1):L308-12. 3. Deneke SM, et al. Increase in endothelial cell glutathione and precursor amino acid uptake by diethyl maleate and hyperoxia. Am J Physiol. 1989 Oct;257(4 Pt 1):L265-71. |
| 保存条件: |
-80℃(运输条件:冰袋低温运输) |
| 配置溶液浓度参考: |
|
1mg |
5mg |
10mg |
| 1 mM |
5.808 ml |
29.039 ml |
58.079 ml |
| 5 mM |
1.162 ml |
5.808 ml |
11.616 ml |
| 10 mM |
0.581 ml |
2.904 ml |
5.808 ml |
| 50 mM |
0.116 ml |
0.581 ml |
1.162 ml |
|
| 注意: |
部分产品我司仅能提供部分信息,我司不保证所提供信息的权威性,仅供客户参考交流研究之用。 |