
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)






规格 | 价格/人民币 | 库存 | 数量 |
2MG | ¥491 | 有现货 |
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5MG | ¥719 | 有现货 |
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10MG | ¥1195 | 有现货 |
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25MG | ¥2479 | 有现货 |
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50MG | ¥3832 | 有现货 |
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100MG | ¥5531 | 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GSK2643943A
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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。
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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) .
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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.
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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.
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同义词——
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通路Proteasome/Ubiquitin
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靶点DUB
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受体DUB
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研究领域——
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适应症——
化学信息
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CAS Number2449301-27-1
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分子量277.3
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分子式C17H12FN3
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纯度>98% (HPLC)
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溶解度In Vitro:?DMSO 中的溶解度 : ≥ 125 mg/mL (450.78 mM )
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SMILESNc1[nH]c2cc(\C=C\c3cccc(F)c3)ccc2c1C#N
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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. 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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