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GSK2643943A

CAS No. 2449301-27-1

GSK2643943A ( —— )

产品货号. M32951 CAS No. 2449301-27-1

GSK2643943A 是一种靶向 USP20 的去泛素化酶 (DUB) 抑制剂。GSK2643943A 对 USP20/Ub-Rho 具有亲和力, 其 IC50 值为 160 nM。GSK2643943A 具有抗肿瘤作用,可用于口腔鳞状细胞癌 (OSCC) 的研究。

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
2MG ¥491 有现货
5MG ¥719 有现货
10MG ¥1195 有现货
25MG ¥2479 有现货
50MG ¥3832 有现货
100MG ¥5531 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
    GSK2643943A
  • 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
    GSK2643943A 是一种靶向 USP20 的去泛素化酶 (DUB) 抑制剂。GSK2643943A 对 USP20/Ub-Rho 具有亲和力, 其 IC50 值为 160 nM。GSK2643943A 具有抗肿瘤作用,可用于口腔鳞状细胞癌 (OSCC) 的研究。
  • 产品描述
    GSK2643943A is a deubiquitinating enzyme (DUB) inhibitor targeting USP20. GSK2643943A has affinity with an IC50 of 160 nM for USP20/Ub-Rho. GSK2643943A has anti-tumor efficacy and can be used for the research of oral squamous cell carcinoma (OSCC) .
  • 体外实验
    Cell Viability Assay Cell Line:SCC9 cells Concentration:1 μM, 5 μM (GSK+0.01 MOI T1012) 1 μM (GSK+0.01 MOI/ 1 MOI T1012)Incubation Time:overnight Result:Displayed a significant drop in viability (R50%) (5 μM GSK+0.01 MOI T1012 infection) and 50% loss of SCC9 viability (1 μM GSK+0.01 MOI T1012 infection) .Remarkably reduced the viability of SCC9 upon exposure to 1 MOI T1012G infection.Western Blot Analysis Cell Line:SCC9 cells Concentration:1 μM Incubation Time:3h, 9 h and 20 h Result: Generally up-regulated the expression of viral proteins at various phases.RT-PCR Cell Line:SCC9 cells Concentration:1 μM Incubation Time:9 h Result: Significantly increased the accumulation of viral ICP8 and VP16 Mrna in SCC9 cells.
  • 体内实验
    Animal Model:The subcutaneous xenograft model.(SCC9 or SCC7 cells (8×106 cells or 1×106 cells), 5-week-old, female, BALB/c nude mice or C3H/HeN mice, four groups, n = 6-7, per group)Dosage:5 mg/kg Administration: GSK2643943A (alone): intraperitoneal administration, daily, for 6 days.GSK2643943A (combination): intraperitoneal administration, daily for 6 days + intratumoral injection with 50 mL of 1×106PFU T1012G in PBS on day 1, day 4, and day 7.Result:Caused a visible drop of tumor volumes and significantly reduced the tumor volumes in mice with combined treatment of GSK2643943A and oHSV-1 T1012G. Increased slightly viral ICP0 and gD mRNA accumulation in SCC9 tumors.Animal Model:The SCC7 mouse model.Dosage:2.5 mg/kg Administration:GSK2643943A (alone): intraperitoneal administration, daily, for 9 days. GSK2643943A (combination): intraperitoneal administration, daily, for 9 days + intratumoral injection, with 50 mL of 1×107PFU T1012G in PBS on days 1, 4, 7, and 10.Result:Caused a visible drop of tumor volumes, significantly reduced in mice with combined treatment of GSK and oHSV-1 T1012G.Increased slightly viral ICP0 and gD mRNA accumulation in SCC7 tumors.
  • 同义词
    ——
  • 通路
    Proteasome/Ubiquitin
  • 靶点
    DUB
  • 受体
    DUB
  • 研究领域
    ——
  • 适应症
    ——

化学信息

  • CAS Number
    2449301-27-1
  • 分子量
    277.3
  • 分子式
    C17H12FN3
  • 纯度
    >98% (HPLC)
  • 溶解度
    In Vitro:?DMSO 中的溶解度 : ≥ 125 mg/mL (450.78 mM )
  • SMILES
    Nc1[nH]c2cc(\C=C\c3cccc(F)c3)ccc2c1C#N
  • 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. Nishi Kumari, et al. Targeting the Ubiquitin Proteasome System in Cancer. Shahzad, Hafiz Naveed (2018). Neoplasm Targeting the Ubiquitin Proteasome System in Cancer. , 10.5772/intechopen.69560(Chapter 8).
产品手册
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