
Sepin-1
CAS No. 163126-81-6
Sepin-1 ( Sepin 1 | Sepin1 | 2H-Benzimidazole, 2,2-dimethyl-5-nitro-, 1,3-dioxide )
产品货号. M27925 CAS No. 163126-81-6
Sepin-1 是分离酶的非竞争性抑制剂,IC50 为 14.8 μM。 Sepin-1可以通过抑制细胞增殖和诱导细胞凋亡来抑制小鼠和人类癌细胞系中乳腺癌异种移植肿瘤的生长。
纯度: >98% (HPLC)






规格 | 价格/人民币 | 库存 | 数量 |
5MG | ¥648 | 有现货 |
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10MG | ¥1037 | 有现货 |
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25MG | ¥2341 | 有现货 |
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50MG | ¥3872 | 有现货 |
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100MG | ¥5581 | 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Sepin-1
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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Sepin-1 是分离酶的非竞争性抑制剂,IC50 为 14.8 μM。 Sepin-1可以通过抑制细胞增殖和诱导细胞凋亡来抑制小鼠和人类癌细胞系中乳腺癌异种移植肿瘤的生长。
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产品描述Sepin-1 is a noncompetitive inhibitor of separase with an IC50 of 14.8 μM. Sepin-1 can inhibit the growth of breast cancer xenograft tumors in mice and human cancer cell lines by inhibiting cell proliferation and inducing apoptosis.
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体外实验Cell Proliferation Assay Cell Line:BT-474, MCF7, MDA-MB-231, MDA-MB-468 cells Concentration:0-64 μM Incubation Time:3 days Result:Inhibited cell growth with EC50s of 18.03, 17.66, 27.33, 27.92 μM for BT-474, MCF7, MDA-MB-231, MDA-MB-468 cells, respectively.Western Blot Analysis Cell Line:BT-474, MCF7, MDA-MB-231, MDA-MB-468 cells Concentration:0, 10, 20, 40 μM Incubation Time:24 h Result:Decreased the expression of FoxM1 protein in a dose-dependent manner, and decreased teh expression of A-Raf, B-Raf, and C-Raf.
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体内实验Animal Model:SCID beige mice (MCF7 xenografts)Dosage:10 mg/kg Administration:I.v.; daily for 5 days a week for 3 weeks Result:Inhibited tumor growth.
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同义词Sepin 1 | Sepin1 | 2H-Benzimidazole, 2,2-dimethyl-5-nitro-, 1,3-dioxide
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通路Others
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靶点Other Targets
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受体Endogenous Metabolite
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研究领域——
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适应症——
化学信息
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CAS Number163126-81-6
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分子量223.188
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分子式C9H9N3O4
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纯度>98% (HPLC)
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溶解度In Vitro:?DMSO : 100 mg/mL (448.05 mM)
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SMILESCC1(C)[N+]([O-])=c2ccc(cc2=[N+]1[O-])[N+]([O-])=O
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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.P F Li, et al. [Inhibitory effect of 2-(N-acetyl-methyl amino)-3',4'-methylenedioxyacetyl-aminophene(SY-640) on covalent binding of carcinogenic benzo(a)pyrene with mouse hepatocyte nuclear DNA]. Yao Xue Xue Bao. 1997 Sep;32(9):663-8.
产品手册




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