CAS NO: | 50-81-7 |
包装 | 价格(元) |
10mM (in 1mL DMSO) | 电议 |
1g | 电议 |
Physical Appearance | A solid |
Storage | Store at -20°C |
M.Wt | 176.12 |
Cas No. | 50-81-7 |
Formula | C6H8O6 |
Solubility | ≥12.2 mg/mL in EtOH with ultrasonic; ≥5.8 mg/mL in DMSO; ≥57.9 mg/mL in H2O |
Chemical Name | (R)-5-((S)-1,2-dihydroxyethyl)-3,4-dihydroxyfuran-2(5H)-one |
Canonical SMILES | O[C@@H](CO)[C@H](C(O)=C1O)OC1=O |
运输条件 | 蓝冰运输或根据您的需求运输。 |
一般建议 | 为了使其更好的溶解,请用37℃加热试管并在超声波水浴中震动片刻。不同厂家不同批次产品溶解度各有差异,仅做参考。若实验所需浓度过大至产品溶解极限,请添加助溶剂助溶或自行调整浓度。溶液形式一般不宜长期储存,请尽快用完。 |
Vitamin C, a water-soluble vitamin, typically functions in the prevention and treatment of the common cold, hypersensitivity and viral infection. It has also been used as an auxiliary treatment for patients with cancer [1].
In CT26 murine colon cancer cells, 100 and 200 μg/ml Vitamin C significantly inhibited tumor cell proliferation. When concentrations of Vitamin C exceeded 200 μg/ml, tumor cells underwent apparent apoptosis. At concentrations of 200, 500 and 1000 μg/ml, Vitamin C markedly induced tumor cell apoptosis, in a dose-dependent manner. In addition, synergistic inhibitory effects of vitamin C (200 μg/ml) and Cisplatin (1 mg/ml) against CT26 tumor cells were observed [1].
In CT26 tumor-bearing BALB/c mice, tumor volume substantially decreased in the high-dose group (2, 4 and 6 mg during 8 ~ 11, 14 ~ 17 and 20 ~ 23 d after inoculation, respectively). Significant diminution of 4T1 tumor growth could also be observed following low- (1, 2, 3 and 4 mg during 8 ~ 11, 14 ~ 17, 20 ~ 23 and 26 ~ 29 d after inoculation, respectively) and high-dose (2, 4, 6 and 8 mg during 8 ~ 11, 14 ~ 17, 20 ~ 23 and 26 ~ 29 d after inoculation, respectively) Vitamin C treatment [1].
Reference:
[1]. Wang G, Yin T, Wang Y. In vitro and in vivo assessment of high-dose vitamin C against murine tumors. Experimental and Therapeutic Medicine, 2016, 12(5): 3058-3062.