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折扣/货期| 货号：AG-CR1-3651-C500 | 规格：500 ug | 目录价：￥1680 |
产品详情
* 以下信息仅供参考，详情请以原厂网站为准
产品名称:
DYRK1A/B Inhibitor AnnH75
别名:
2-(1-Chloro-7-methoxy-9H-pyrido[3,4-b]indol-9-yl)acetonitrile; AnnH75
产品描述:
Potent selective membrane-permeable DYRK1A (IC50=181nM) and DYRK1B inhibitor. Off-target inhibition of CLK1, CLK4 and Haspin/GSG2. Shows no inhibitory effects on monoamine oxidase A (MAO A). Inhibited the cotranslational tyrosine autophosphorylation of DYRK1A and threonine phosphorylation of an exogenous substrate protein with similar potency. Dose-dependently reduced the phosphorylation of three known DYRK1A substrates (SF3B1, SEPT4 and tau) without negative effects on cell viability in celular assays. Moderate inhibitor of CDK8, CLK2, GRK4, MEK2, PIM1, PIM3 and PKCepsilon. Shows minimal cytotoxic effects in HeLa and PC12 cells up to 10µM. The pleiotropic protein kinase DYRK1A has diverse functions in cell cycle control, neuronal differentiation and synaptic transmission and has attracted increasing interest as a potential drug target, due to its role in the pathology of Down syndrome, neurodegenerative diseases such as Alzheimer's disease and cancer. The closely related kinase DYRK1B has been associated with cancer cell survival by arresting cells in a quiescent state to allow cellular repair and mutations in DYRK1B might be causative in metabolic syndrome.
保存温度:
+4°C
运输温度:
Ambient
预期分子量:
271.7
产品形式:
solid
有效期:
Stable for at least 2 years after receipt when stored at -20°C.
产地:
瑞士
纯度:
>98% (HPLC, NMR)
分子式:
C14H10ClN3O
溶解度:
Soluble in DMSO.
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