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首页- Products - Apoptosis - Apoptosis - 1-(4-Chloro-3-(trifluoromethyl)phenyl)-3-(4-(4-cyanophenoxy)phenyl)urea

1-(4-Chloro-3-(trifluoromethyl)phenyl)-3-(4-(4-cyanophenoxy)phenyl)urea

CAS No. 1313019-65-6

1-(4-Chloro-3-(trifluoromethyl)phenyl)-3-(4-(4-cyanophenoxy)phenyl)urea ( SC-1 )

产品货号. M27576 CAS No. 1313019-65-6

SC-1 是多种酪氨酸激酶抑制剂索拉非尼的衍生物。 SC-1 通过阻断 STAT3 磷酸化和激活来有效抑制 STAT3 磷酸化,并诱导肝细胞癌细胞系凋亡。

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
5MG ¥2203 有现货
10MG ¥3467 有现货
25MG ¥6302 有现货
50MG ¥9072 有现货
100MG ¥12069 有现货
200MG 获取报价 有现货
500MG 获取报价 有现货
1G 获取报价 有现货

生物学信息

  • 产品名称
    1-(4-Chloro-3-(trifluoromethyl)phenyl)-3-(4-(4-cyanophenoxy)phenyl)urea
  • 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
  • 产品简述
    SC-1 是多种酪氨酸激酶抑制剂索拉非尼的衍生物。 SC-1 通过阻断 STAT3 磷酸化和激活来有效抑制 STAT3 磷酸化,并诱导肝细胞癌细胞系凋亡。
  • 产品描述
    SC-1 is a a derivative of the multiple tyrosine kinase inhibitor sorafenib. SC-1 potently inhibits the phosphorylation of STAT3 by blocking STAT3 phosphorylation and activation, and induces apoptosis in hepatocellular carcinoma cell lines.(In Vitro):SC-1(1-10 μM; 48 hours; breast cancer cells) treatment demonstrates dose-dependent suppression of cell viability in all tested breast cancer cells. SC-1(1-10 μM; 36 hours; breast cancer cells) treatment induces potent apoptotic activity in association with downregulation of p-STAT3 and its downstream proteins cyclin D1 and survivin in a dose-dependent manner in breast cancer cell lines.(In Vivo):SC-1 showes efficacious antitumor activity and p-STAT3 downregulation in MDA-MB-468 xenograft tumors in vivo.
  • 体外实验
    STAT3-IN-7 (SC-1; 1-10 μM; 48 hours; breast cancer cells) treatment demonstrates dose-dependent suppression of cell viability in all tested breast cancer cells.STAT3-IN-7 (SC-1; 1-10 μM; 36 hours; breast cancer cells) treatment induces potent apoptotic activity.STAT3-IN-7 (SC-1; 1-10 μM; 36 hours; breast cancer cells) treatment shows downregulation of p-STAT3 and its downstream proteins cyclin D1 and survivin in a dose-dependent manner in breast cancer cell lines. Cell Viability AssayCell Line:HCC-1937, MDA-MB-231, MDA-MB-468, MDA-MB-453, SK-BR3 and MCF-7 cells Concentration:1 μM, 2 μM, 5 μM, 7.5 μM, 10 μM Incubation Time:48 hours Result:Demonstrated dose-dependent suppression of cell viability in all tested breast cancer cells.Apoptosis Analysis Cell Line:HCC-1937, MDA-MB-231, MDA-MB-468, MDA-MB-453, SK-BR3 and MCF-7 cells Concentration:1 μM, 2 μM, 5 μM, 7.5 μM, 10 μM Incubation Time:36 hours Result:Induced potent apoptotic activity.Western Blot Analysis Cell Line:HCC-1937, MDA-MB-231, MDA-MB-468, MDA-MB-453, SK-BR3 and MCF-7 cells Concentration:1 μM, 2 μM, 5 μM, 7.5 μM, 10 μM Incubation Time:36 hoursResult:Showed downregulation of p-STAT3 and its downstream proteins cyclin D1 and survivin in a dose-dependent manner in breast cancer cell lines.
  • 体内实验
    STAT3-IN-7 (10 mg/kg; oral gavage; daily; for 28 days; female NCr athymic nude mice) treatment shows efficacious antitumor activity and p-STAT3 downregulation in MDA-MB-468 xenograft tumors. Animal Model:Female NCr athymic nude mice (4-6 weeks of age) injected with breast cancer cells Dosage:10 mg/kg Administration:Oral gavage; daily; for 28 days Result:Showed efficacious antitumor activity and p-STAT3 downregulation in MDA-MB-468 xenograft tumors.
  • 同义词
    SC-1
  • 通路
    Apoptosis
  • 靶点
    Apoptosis
  • 受体
    HCV|Bacterial|Apoptosis|Fungal
  • 研究领域
    ——
  • 适应症
    ——

化学信息

  • CAS Number
    1313019-65-6
  • 分子量
    431.8
  • 分子式
    C21H13ClF3N3O2
  • 纯度
    >98% (HPLC)
  • 溶解度
    In Vitro:?DMSO : 250 mg/mL (578.97 mM)
  • SMILES
    N#Cc(cc1)ccc1Oc(cc1)ccc1NC(Nc(cc1)cc(C(F)(F)F)c1Cl)=O
  • 化学全称
    ——

运输与储存

  • 储存条件
    (-20℃)
  • 运输条件
    With Ice Pack
  • 稳定性
    ≥ 2 years

参考文献

1.Satoru Tamura, et al. Oenothein B, dimeric hydrolysable tannin inhibiting HCV invasion from Oenothera erythrosepala. J Nat Med. 2019 Jan;73(1):67-75.
产品手册
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