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Se-Aspirin
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
Se-Aspirin图片
CAS NO:1850293-95-6
包装与价格:
包装价格(元)
5mg电议
10mg电议
50mg电议

产品介绍

化学性质

Physical AppearanceA crystalline solid
StorageStore at -20°C
M.Wt311.2
Cas No.1850293-95-6
FormulaC12H12N2O3Se
SynonymsSelenium-acetylsalicylic Acid
Solubility≤10mg/ml in ethanol;30mg/ml in DMSO;50mg/ml in dimethyl formamide
Chemical Nameselenocyanic acid, 2-[[2-(acetyloxy)benzoyl]amino]ethyl ester
Canonical SMILESO=C(C)OC1=CC=CC=C1C(NCC[Se]C#N)=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。

资料参考

Se-Aspirin is a novel selenium-nonsteroidal anti-inflammatory drug (Se-NSAID) [1].

NSAIDs have demonstrated intestinal antineoplastic effects in various animal intestinal cancer models. Selenium (Se) compounds have attracted a vast interest as promising chemo-preventive agents. Several epidemiological studies have reported an inverse association between the nutritional Se status and cancer risk. Se functioned as chemo-preventive agent for cancer therapy in the past few years.

Se-Aspirin was a hybrid of selenium and a nonsteroidal anti-inflammatory drug. t Se-Aspirin reduced the viability of different cancer cell lines, particularly colorectal cancer (CRC) cells with the IC50 value of 3.4 μM. Se-Aspirin inhibited the cell cycle in G1 and G2/M phases and induced apoptosis by activating caspase 3/7 and PARP cleavage. Long-term exposure to Se-Aspirin has been reported to cause an increase in intracellular reactive oxygen species levels in CRC cells [1].

Reference:
[1] Plano D, Karelia D N, Pandey M K, et al.  Design, synthesis, and biological evaluation of novel selenium (Se-NSAID) molecules as anticancer agents[J]. Journal of medicinal chemistry, 2016, 59(5): 1946-1959.