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首頁 > 產品目錄 > 信號通路 > Cell Cycle | 細胞周期 > PERK > 1-(5-(4-氨基-7-甲基-7H-吡咯并[2,3-d]嘧啶-5-基)二氫吲哚-1-基)-2-(3-(三氟甲基)苯基)乙酮

1-(5-(4-氨基-7-甲基-7H-吡咯并[2,3-d]嘧啶-5-基)二氫吲哚-1-基)-2-(3-(三氟甲基)苯基)乙酮

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1-(5-(4-Amino-7-methyl-7H-pyrrolo[2,3-d]pyrimidin-5-yl)indolin-1-yl)-2-(3-(trifluoromethyl)phenyl)ethanone;GSK2606414 (Synonyms: GSK 2606414)

產品編號:CL1098 CAS No.:1337531-36-8 MDLNo: 分子式:C24H20F3N5O 分子量:451.44
規(guī)格 庫存 目錄價 會員專享價 數(shù)量
20 mg In-stock ¥520.00 登錄后可見
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50 mg In-stock ¥850.00 登錄后可見
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100 mg In-stock ¥1450.00 登錄后可見
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基本信息
英文名稱 1-(5-(4-Amino-7-methyl-7H-pyrrolo[2,3-d]pyrimidin-5-yl)indolin-1-yl)-2-(3-(trifluoromethyl)phenyl)ethanone;GSK2606414 (Synonyms: GSK 2606414)
中文名稱1-(5-(4-氨基-7-甲基-7H-吡咯并[2,3-d]嘧啶-5-基)二氫吲哚-1-基)-2-(3-(三氟甲基)苯基)乙酮
CAS號1337531-36-8
分子式C24H20F3N5O
分子量451.44
外觀White powder
儲存條件 Dry, dark and at 0 - 4 ℃ for short term (days to weeks) or -20 ℃ for long term (months to years).
產品詳情

GSK2606414 is an orally available, selective protein kinase R-like ER kinase (PERK) inhibitor with an IC50 value of 0.4 nM. It can inhibit thapsigargin-induced PERK phosphorylation in lung carcinoma A549 cells and attenuates subcutaneous pancreatic human tumor xenograft growth in mice. Because PERK mediates the unfolded protein response pathway, which has roles in neurotoxicity and cancer, inhibition of PERK signaling has potential applications for the treatment of cancer and also cognitive degeneration.


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