FEN1 Inhibitor C2
CAS No. 1995893-58-7
FEN1 Inhibitor C2 ( FEN1-IN-4 )
产品货号. M22114 CAS No. 1995893-58-7
FEN1-IN-4 是人皮瓣核酸内切酶 1 (hFEN1) 的抑制剂。FEN1 抑制剂 C2 抑制选择性损害缺乏 Cdc4 和 Mre11a 的结肠癌细胞的增殖,这两种细胞在结直肠癌中经常发生突变。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 2MG | ¥462 | 有现货 |
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| 5MG | ¥721 | 有现货 |
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| 10MG | ¥1158 | 有现货 |
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| 25MG | ¥2049 | 有现货 |
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| 50MG | ¥3216 | 有现货 |
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| 100MG | ¥4965 | 有现货 |
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| 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
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产品名称FEN1 Inhibitor C2
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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FEN1-IN-4 是人皮瓣核酸内切酶 1 (hFEN1) 的抑制剂。FEN1 抑制剂 C2 抑制选择性损害缺乏 Cdc4 和 Mre11a 的结肠癌细胞的增殖,这两种细胞在结直肠癌中经常发生突变。
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产品描述FEN1-IN-4 is an inhibitor of human flap endonuclease-1 (hFEN1)FEN1 Inhibitor C2 inhibition selectively impairs proliferation of colon cancer cells deficient in Cdc4 and Mre11a, both frequently mutated in colorectal cancers.?FEN1 has also emerged as a potential chemosensitizing target due to its role in LP-BER since it is critical for repair of MMS (methyl methanesulfonate)-induced alkylation damage, and its knockdown or inhibition increases sensitivity to TMZ (temozolomide) in glioblastoma and colorectal cancer cell lines.
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体外实验FEN1 inhibition selectively impairs proliferation of colon cancer cells deficient in Cdc4 and Mre11a, both frequently mutated in colorectal cancers. FEN1 has also emerged as a potential chemosensitizing target due to its role in LP-BER since it is critical for repair of Methyl methanesulfonate-induced alkylation damage, and its knockdown or inhibition increases sensitivity to Temozolomide in glioblastoma and colorectal cancer cell lines.
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体内实验——
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同义词FEN1-IN-4
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通路Others
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靶点Other Targets
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受体hFEN1
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研究领域——
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适应症——
化学信息
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CAS Number1995893-58-7
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分子量232.24
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分子式C12H12N2O3
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纯度>98% (HPLC)
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溶解度DMSO:100 mg/mL (430.59 mM; Need ultrasonic)
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SMILESOn1c(=O)n(CC2CC2)c2ccccc2c1=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.Jack C Exell, et al. Cellularly Active N-hydroxyurea FEN1 Inhibitors Block Substrate Entry to the Active Site. Nat Chem Biol. 2016 Oct;12(10):815-21.
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