CAS NO: | 565-73-1 |
包装 | 价格(元) |
5g | 电议 |
10g | 电议 |
25g | 电议 |
50g | 电议 |
Storage | Store at -20°C |
M.Wt | 111.03 |
Cas No. | 565-73-1 |
Formula | C2H2NNaO3 |
Solubility | insoluble in EtOH; insoluble in DMSO; ≥11.1 mg/mL in H2O |
Chemical Name | sodium 2-amino-2-oxoacetate |
Canonical SMILES | [O-]C(C(N)=O)=O.[Na+] |
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。 |
Sodium oxamate is a competitive LDHA(actate dehydrogenase A) inhibitor, sodium oxamate is a derivative of pyruvate that inhibits the conversion of pyruvate to lactate via lactate dehydrogenase, thus disrupting glycolysis. Because cancer cells produce a large amount of energy via aerobic glycolysis, sodium oxamate has been studied as an inhibitor of carbohydrate metabolism in various tumors[1,2].
References:
[1]. Anna Z K, De S M M L, Antonio S, et al. Modulation of Cell Metabolic Pathways and Oxidative Stress Signaling Contribute to Acquired Melphalan Resistance in Multiple Myeloma Cells. PLOS ONE, 2015, 10(3): e0119857.
[2]. Cui J, Shi M, Xie D, et al. FOXM1 promotes the warburg effect and pancreatic cancer progression via transactivation of LDHA expression. Clinical Cancer Research, 2014, 20(10): 2595-2606.