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Melatonin-d7是Melatonin的氘代物。Melatonin是由松果体合成的激素,能够激活褪黑激素受体,对睡眠过程有作用并具备显著的抗氧化和抗炎特性。Melatonin作为一种新型的选择性ATF-6抑制剂,通过COX-2下调来诱导人肝癌细胞凋亡。它还通过内质网应激减轻palmitic acid-induced诱导的小鼠颗粒细胞的凋亡。

Melatonin-d7是Melatonin的氘代物。Melatonin是由松果体合成的激素,能够激活褪黑激素受体,对睡眠过程有作用并具备显著的抗氧化和抗炎特性。Melatonin作为一种新型的选择性ATF-6抑制剂,通过COX-2下调来诱导人肝癌细胞凋亡。它还通过内质网应激减轻palmitic acid-induced诱导的小鼠颗粒细胞的凋亡。
| 规格 | 价格 | 库存 | 数量 |
|---|---|---|---|
| 10 mg | 待询 | 待询 | |
| 50 mg | 待询 | 待询 |
| 产品描述 | Melatonin-d7 is the deuterated form of melatonin. Melatonin is a hormone produced by the pineal gland that activates melatonin receptors. It plays a role in sleep and possesses significant antioxidant and anti-inflammatory properties. As a novel selective ATF-6 inhibitor, melatonin induces apoptosis in human liver cancer cells by downregulating COX-2. Additionally, melatonin mitigates palmitic acid-induced apoptosis in mouse granulosa cells through endoplasmic reticulum stress. |
| 分子量 | 239.32 |
| 分子式 | C13H16N2O2 |
| CAS No. | 615251-68-8 |
| Smiles | C(C(NC(C([2H])([2H])[2H])=O)([2H])[2H])(C=1C=2C(NC1)=CC=C(OC)C2)([2H])[2H] |
| 存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. |
以上为“体内实验配液计算器”的使用方法举例,并不是具体某个化合物的推荐配制方式,请根据您的实验动物和给药方式选择适当的溶解方案。
对于不同动物的给药剂量换算,您也可以参考 更多