
SSE15206
CAS No. 1370046-40-4
SSE15206 ( —— )
产品货号. M20392 CAS No. 1370046-40-4
SSE15206是一种克服多药耐药性的微管聚合抑制剂。由于癌细胞中纺锤体形成不完整,导致异常有丝分裂,导致 G2/M 期停滞。
纯度: >98% (HPLC)






规格 | 价格/人民币 | 库存 | 数量 |
2MG | ¥332 | 有现货 |
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5MG | ¥486 | 有现货 |
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10MG | ¥632 | 有现货 |
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25MG | ¥1272 | 有现货 |
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50MG | ¥1952 | 有现货 |
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100MG | ¥3054 | 有现货 |
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200MG | 获取报价 | 有现货 |
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500MG | 获取报价 | 有现货 |
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1G | 获取报价 | 有现货 |
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生物学信息
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产品名称SSE15206
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注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
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产品简述SSE15206是一种克服多药耐药性的微管聚合抑制剂。由于癌细胞中纺锤体形成不完整,导致异常有丝分裂,导致 G2/M 期停滞。
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产品描述SSE15206 is a microtubule polymerization inhibitor that overcomes multidrug resistance. Causes aberrant mitosis resulting in G2/M arrest due to incomplete spindle formation in cancer cells.
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体外实验SSE15206 induces apoptosis in cells irrespective of MDR-1 overexpression cell lines (KB-V1, A2780-Pac-Res), highly resistant to paclitaxel cells (HCT116-Pac-Res) and parental cells at the concentration of 5 × and 10 × GI50 values. To conclude, SSE15206 is able to overcome resistance to chemotherapeutic drugs such as paclitaxel in different cancer cell lines. Western Blot Analysis Cell Line:Drug-resistant cell lines (KB-V1, A2780-Pac-Res, HCT116-Pac-Res) and parental cells. Concentration:5 × and 10 × GI50 values (GI50=197 nM in HCT-116 cells).Incubation Time:24 hours.Result:Induced apoptosis in cells irrespective of MDR-1 overexpression and HCT116-Pac-Res and parental cells.
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体内实验——
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同义词——
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通路Cytoskeleton/Cell Adhesion Molecules
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靶点Microtubule/Tubulin
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受体microtubule
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研究领域——
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适应症——
化学信息
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CAS Number1370046-40-4
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分子量371.45
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分子式C19H21N3O3S?
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纯度>98% (HPLC)
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溶解度DMSO:150 mg/mL (403.82 mM)
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SMILESCOc1cc(cc(OC)c1OC)C1CC(=NN1C(N)=S)c1ccccc1
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化学全称45-Dihydro-3-phenyl-5-(345-trimethoxyphenyl)-1H-pyrazole-1-carbothioamide
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
1.Manzoor S Bilal A Khan S et al. Identification and characterization of SSE15206 a microtubule depolymerizing agent that overcomes multidrug resistance[J]. Scientific Reports 2018 8(1).
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