Sodium oxamate (Synonyms:草氨酸钠;Oxamic acid sodium)
目录号 : KCM14317 CAS No. : 565-73-1 纯度 : ≥95%
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.
规格 价格 是否有货 数量
500mg
In-stock
1g
In-stock
5g
In-stock
25g
In-stock

Other Forms of Rapamycin:

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体外研究

Oxamate acid inhibits the proliferation, migration, and invasion of A2780 and SKOV3 cells
Oxamate acid (10 μ M; 24-72 h) exhibits dose-dependent and time-dependent inhibition of cell proliferation in two types of NPC cancer cells
Sodium Oxamate (0-100 mM; 24 hours) induces G2/M phase cell cycle arrest in CNE-1 and CNE-2 cells
Sodium Oxamate (0-100 mM; 48 hours) induces apoptosis in NPC cells through caspase-3 activation and mitochondrial pathway
Sodium Oxamate (0-100 mM; 24 hours) increases ROS levels in NPC cells

 

Cell Proliferation Assay

Cell Line: CNE-1 and CNE-2 cells
Concentration: 10 μM
Incubation Time: 24-72 hours
Result: Showed IC50s of 74.6, 32.4 and 17.8 mM and 62.3, 44.5, 31.6 mM at 24, 48 and 72 h in the CNE-1 and CNE-2 cancer cells, respectively.
体内研究

Sodium Oxamate (intraperitoneal injection; 750 mg/kg; Every time; 3 w) Combined radiation treatment can enhance the tumor suppression effect in vivo.

 

Animal Model: Female Balb/c nude mice injected with CNE-1 cells
Dosage: 750 mg/kg
Administration: Intraperitoneal injection; 750 mg/kg; once daily; 3 weeks
Result: Inhibited the tumor growth when compared to either oxamate alone or irradiation alone.
 
分子式
C2H2NNaO3
分子量
111.03
CAS号
565-73-1
中文名称
草氨酸钠
运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

2-8°C, sealed storage, away from moisture

* In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)

溶解性数据
In Vitro: 

DMSO : 3.23 mg/mL (29.09 mM; ultrasonic and warming and adjust pH to 5 with HCl and heat to 60°C)

H2O : 50 mg/mL (450.33 mM; Need ultrasonic)

配制储备液
浓度 溶剂体积 质量 1 mg 5 mg 10 mg
1 mM 9.0066 mL 45.0329 mL 90.0658 mL
5 mM 1.8013 mL 9.0066 mL 18.0132 mL
10 mM 0.9007 mL 4.5033 mL 9.0066 mL
*

请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。
储备液的保存方式和期限:-80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)。-80°C 储存时,请在 6 个月内使用,-20°C 储存时,请在 1 个月内使用。

In Vivo:

请根据您的实验动物和给药方式选择适当的溶解方案。以下溶解方案都请先按照 In Vitro 方式配制澄清的储备液,再依次添加助溶剂:

——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议您现用现配,当天使用; 以下溶剂前显示的百
分比是指该溶剂在您配制终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶

  • 1.

    请依序添加每种溶剂:  Saline

    Solubility: 75 mg/mL (675.49 mM); Suspended solution; Need ultrasonic

纯度: ≥95%

The molarity calculator equation
Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)
The dilution calculator equation
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
This equation is commonly abbreviated as: C1V1 = C2V2