Misonidazole

目录号: GC16331纯度: >95.00%同义词: 米索硝唑,NSC 261037,Ro 7-0582,SR 1354
A nitroimidazole that targets hypoxic cells

Misonidazole
Cas No.: 13551-87-6
规格价格库存数量操作
1mg¥955.00现货
1
5mg¥1,648.00现货
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10mg¥2,325.00现货
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25mg¥2,703.00现货
1

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产品描述 Description

Misonidazole (MISO), a hypoxic cell radiosensitizer, is selectively metabolized by hypoxic cells to reactive products that bind covalently to cellular constituents. The drug also possesses a substantial cytotoxic effect, independent of radiation, which is selectively expressed in hypoxic cells. Misonidazole may be cytotoxic to the normal hypoxic tissues in the human body, making this became a major concern in the clinical application of the drug. Misonidazole leads to strand breaks in cellular DNA and those cells which fail to survive also fail to repair these strand breaks. Misonidazole depletes intracellular glutathione and is more toxic in glutathione depleted cells. The depletion is time, temperature, drug concentration and cell line dependent.

In vitro: In cultured CHO cells, pretreatment with 5 mM MISO for 2 hr exihibited the marginal toxicity [2].

In vivo: Pretreatment with misonidazole (MISO) enhanced the number of cross-links formed in a fibrosarcoma and in the spleen and gut of mice for periods up to 48 h following a single injection of melphalan (MEL). MISO pretreatment could result in a greater amount of binding of MEL to DNA at early times after injection. MISO may exert its affect by inhibiting the repair of cross-links or monoadducts at early times post-injection [3].

Clinical trials: Various dose schedules of misonidazole have proven to be tolerable, with a moderate incidence of nausea and vomiting and mild peripheral neuropathy, and a low incidence of more severe peripheral neuropathy or central neuropathy [4].

References:
[1] Josephy P D, Palcic B, Skarsgard L D.  Ascorbate-enhanced cytotoxicity of misonidazole[J]. Nature, 1978, 271(5643): 370-372.
[2]Taylor Y C, Bump E A, Brown J M.  Studies on the mechanism of chemosensitization by misonidazole in vitro[J]. International Journal of Radiation Oncology Biology Physics, 1982, 8(3-4): 705-708.
[3] Murray D, Meyn R E.  Enhancement of the DNA cross-linking activity of melphalan by misonidazole in vivo[J]. British journal of cancer, 1983, 47(2): 195.
[4] Wasserman T H, Stetz J A, Phillips T L.  Clinical trials of misonidazole in the United States[J]. Cancer clinical trials, 1980, 4(1): 7-16.

产品文档 Product Documents

Purity:>95.00%

化学性质Chemical Properties

CAS 号
13551-87-6
同义词
米索硝唑,NSC 261037,Ro 7-0582,SR 1354
化学名
α-(methoxymethyl)-2-nitro-1H-imidazole-1-ethanol
SMILES
OC(COC)CN1C=CN=C1[N+]([O-])=O
分子式
C7H11N3O4
分子量
201.2 g/mol
溶解性
≤5mg/ml in ethanol;15mg/ml in DMSO;15mg/ml in dimethyl formamide
保存条件
Store at -20°C
General tips
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 储存时,请在 6 个月内使用,-20°C 储存时,请在 1 个月内使用。
为了提高溶解度,请将管子加热至 37°C,然后在超声波浴中震荡一段时间。
Shipping Condition
评估样品解决方案:配备蓝冰进行发货。所有其他可用尺寸:配备 RT,或根据请求配备蓝冰。

计算工具摩尔浓度 / 稀释 / 分子量 / 单位换算 / 体内配方 / 溶解度

g/mol