Menadione

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Chemical Structure| 58-27-5 同义名 : 维生素K3 ;Vitamin K3;NSC 4170;Menadione bisulfite;Vikasol;Vicasol;Vitamin K3 sodium bisulfite;Thyloquinone;Menaphthone;2-Methyl-1,4-naphthoquinone
CAS号 : 58-27-5
货号 : A129193
分子式 : C11H8O2
纯度 : 98%
分子量 : 172.18
MDL号 : MFCD00001681
存储条件:

Pure form Keep in dark place,Sealed in dry,Room Temperature

In solvent -20°C:3-6个月-80°C:12个月

溶解度 :

DMSO: 120 mg/mL(696.95 mM),配合低频超声助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO

无水乙醇: 8 mg/mL(46.46 mM),配合低频超声助溶,注意:无水乙醇开封后,易挥发,也会吸收空气中的水分,导致溶解能力下降,请避免使用开封较久的乙醇

动物实验配方:

IP 2% DMSO+2% Tween80+30% PEG300+water 2.6 mg/mL clear

PO 0.5% CMC-Na 30 mg/mL suspension

生物活性
描述 Menadione, a naphthoquinone, transforms into active vitamin K2 within the body. It has potential uses as both an anticancer compound and a radiosensitizer[1].
细胞研究
细胞系 浓度 检测类型 检测时间 活性说明 数据源
CRL2796 cells Cytotoxicity assay Cytotoxicity against human CRL2796 cells assessed as inhibition of formazan formation at day 4 by measuring absorbance at 430 nm, IC50=21 μM 19969400
DU145 cells Cytotoxicity assay 72 h Cytotoxicity against human DU145 cells assessed as growth inhibition after 72 hrs by MTS assay, IC50=9.86 μM 23791367
HaCaT cells Function assay 48 h Antihyperproliferative activity against human HaCaT cells assessed as inhibition of cell growth after 48 hrs by phase contrast microscopy, IC50=15.8 μM 24964246
实验方案
1mg 5mg 10mg

1 mM

5 mM

10 mM

5.81mL

1.16mL

0.58mL

29.04mL

5.81mL

2.90mL

58.08mL

11.62mL

5.81mL

参考文献

[1]Chiou TJ, et al. Cardiac and renal toxicity of menadione in rat. Toxicology. 1997 Dec 31;124(3):193-202.

[2]Sata N, et al. Menadione induces both necrosis and apoptosis in rat pancreatic acinar AR4-2J cells. Free Radic Biol Med. 1997;23(6):844-50.