氯硝柳胺
基本信息
产品名称 | 氯硝柳胺 |
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英文名称 | Niclosamide |
别名 | 2′,5-二氯-4′-硝基水杨酸酰替苯胺 |
英文别名 | 2′,5-Dichloro-4′-nitrosalicylanilide; 5-Chloro-N-(2-chloro-4-nitrophenyl)-2-hydroxybenzamide |
规格或纯度 | 98% |
运输条件 | 常规运输 |
生化机理 | 抗蠕虫药,抗癌药和质子试剂。STAT3抑制剂(IC 50 = 0.25μM)。已显示抑制许多下游信号传导途径,包括mTORC1,Wnt /β-catinin,NF-κB,Notch和ROS。 |
一般描述
Niclosamide is an inhibitor of the Stat3 signaling pathway. Niclosamide inhibits the activation, nuclear translocation and transactivation of Stat3. Niclosamide displays selectivity for Stat3 over Stat1, Stat5, JAK1, JAK2 and Src kinases. Niclosamide inhibits the transcription of Stat3 target genes and induces cell growth inhibition, apoptosis and cell cycle arrest of cancer cells with constitutively active Stat3. Niclosamide is also a FRAP inhibitor via reversible inhibition of mTORC1 signaling and stimulates autophagy in vitro. Niclosamide displays antineoplastic effects in acute myelogenous leukemia (AML) stem cells.An inhibitor of the Stat3 signaling pathway and also a FRAP inhibitor.
Niclosamide is an inhibitor of the Stat3 signaling pathway. Niclosamide inhibits the activation, nuclear translocation and transactivation of Stat3. Niclosamide displays selectivity for Stat3 over Stat1, Stat5, JAK1, JAK2 and Src kinases. Niclosamide inhibits the transcription of Stat3 target genes and induces cell growth inhibition, apoptosis and cell cycle arrest of cancer cells with constitutively active Stat3. Niclosamide is also a FRAP inhibitor via reversible inhibition of mTORC1 signaling and stimulates autophagy in vitro. Niclosamide displays antineoplastic effects in acute myelogenous leukemia (AML) stem cells.
An inhibitor of the Stat3 signaling pathway and also a FRAP inhibitor.
相关属性
CAS编号 | 50-65-7 |
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熔点 | 225-230°C |
溶解性 | Soluble in ethanol (25 mM), DMSO (10 mM), chloroform (very slightly), and methanol: acetone (1: 1) (50 mg/ml). Insoluble in water. |
RTECS | VN8400000 |
MDL号 | MFCD00057597 |
密度 | 1.161 |
分子量 | 327.12 |
分子式 | C13H8Cl2N2O4 |
EC号 | 200-056-8 |
品牌 | Jinpan |
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PubChem CID | 4477 |