GDP366
CAS No. 501698-03-9
GDP366 ( —— )
产品货号. M26230 CAS No. 501698-03-9
GDP366 可诱导人类癌细胞的细胞生长抑制、细胞衰老和有丝分裂灾难。生存素和 Op18 的双重抑制剂。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 5MG | ¥4332 | 有现货 |
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| 10MG | ¥6071 | 有现货 |
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| 25MG | ¥8826 | 有现货 |
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| 50MG | ¥11904 | 有现货 |
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| 100MG | ¥15480 | 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 |
|
| 1 mL x 10 mM in DMSO | ¥4665 | 有现货 |
|
生物学信息
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产品名称GDP366
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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GDP366 可诱导人类癌细胞的细胞生长抑制、细胞衰老和有丝分裂灾难。生存素和 Op18 的双重抑制剂。
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产品描述GDP366, induces cell growth inhibition, cellular senescence and mitotic catastrophe in human cancer cells. a dual inhibitor of survivin and Op18.(In Vitro):GDP366 induces polyploidy in multiple types of cancer cell lines. GDP366 decreass both the mRNA and protein levels of survivin and Op18. This inhibitory effect is not dependent on the status of p53 and p21 although GDP366 potently increases p53 and p21 levels. GDP366 significantly inhibits the growth of tumor cells in vitro and in vivo (nude mouse model) without rapid induction of apoptosis.
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体外实验GDP366 potently and selectively inhibits the expression of both survivin and Op18. GDP366 decreass both the mRNA and protein levels of survivin and Op18. This inhibitory effect is not dependent on the status of p53 and p21 although GDP366 potently increases p53 and p21 levels. GDP366 significantly inhibits the growth of tumor cells in vitro and in vivo (nude mouse model) without rapid induction of apoptosis. GDP366 induces polyploidy in multiple types of cancer cell lines. GDP366 increases chromosomal instability, and induces cellular senescence by inhibiting telomerase activity.
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体内实验——
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同义词——
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通路Others
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靶点Other Targets
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受体Separase
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研究领域——
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适应症——
化学信息
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CAS Number501698-03-9
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分子量375.45
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分子式C20H17N5OS
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纯度>98% (HPLC)
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溶解度In Vitro:?DMSO : 62.5 mg/mL (166.47 mM)
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SMILESCc1cccc(NC(=O)Nc2ccc(cc2)-c2csc3ncnc(N)c23)c1
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化学全称——
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.Do HT, Zhang N, Pati D, Gilbertson SR. Synthesis and activity of benzimidazole-1,3-dioxide inhibitors of separase. Bioorg Med Chem Lett. 2016 Sep 15;26(18):4446-50.
产品手册
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