IEM 1754 DIHYDROBROMIDE
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- CAS号:
- 162831-31-4
- 英文名:
- IEM 1754 dihydrobroMide
- 英文别名:
- CS-975;AOB5933;IEM1754;IEM 1754 2HBr;IEM 1754 DIHYDROBROMIDE;IEM 1754 dihydrobroMide USP/EP/BP;IEM1754 DIHYDROBROMIDE;IEM1754 2 HBR; AOB5933;;N1-(adamantan-1-ylmethyl)pentane-1,5-diamine dihydrobromide;N1-((3r,5r,7r)-Adamantan-1-ylmethyl)pentane-1,5-diamine hydrobromide;1,5-PENTANEDIAMINE, N1-(TRICYCLO[3.3.1.13,7]DEC-1-YLMETHYL)-, HYDROBROMIDE
- 中文名:
- IEM 1754 DIHYDROBROMIDE
- 中文别名:
- 化合物IEM 1754 2HBR;N1-(金刚烷-1-基甲基)戊烷-1,5-二胺二氢溴化物
- CBNumber:
- CB32538278
- 分子式:
- C16H32Br2N2
- 分子量:
- 412.24668
- MOL File:
- 162831-31-4.mol
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IEM 1754 DIHYDROBROMIDE化学性质
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储存条件:
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Store at -20°C
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溶解度:
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Soluble to 100 mM in water and to 50 mM in DMSO
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形态:
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Powder
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IEM 1754 DIHYDROBROMIDE性质、用途与生产工艺
IEM 1754 dihydrobroMide是选择性AMPA/kainate受体抑制剂，作用于GluR1和GluR3，IC50为6 μM。
IEM 1754是一种金刚烷衍生物。IEM 1754可以引起对重组AMPA受体开放通道的使用和电压依赖性阻断。拮抗作用依赖于受体亚单位组成部分, GluR1和GluR3门控通道对阻断的敏感性高于GluR2构成的受体门控通道。与经典的单指数模型一致，IEM-1754对含有GluR2的AMPAR阻断可以被超极化加强。作为对比，IEM-1754对GluR2缺乏的AMPAR阻断可以被超极化减弱。
IEM 1754 DIHYDROBROMIDE
上下游产品信息
上游原料
下游产品
IEM 1754 DIHYDROBROMIDE
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162831-31-4, IEM 1754 DIHYDROBROMIDE 相关搜索:
- Inhibitors
- 药靶配体
- 小分子抑制剂，天然产物
- C16H30N22HBr
- C16H31BrN2
- N1-(金刚烷-1-基甲基)戊烷-1,5-二胺二氢溴化物
- 化合物IEM 1754 2HBR
- 162831-31-4
- N1-(adamantan-1-ylmethyl)pentane-1,5-diamine dihydrobromide
- AMPA receptor,channel block,IEM 1754,Ionotropic glutamate receptors,voltage dependence,IEM1754,inhibit,iGluR,Inhibitor,IEM 1754 2HBr,NMDA receptor,IEM-1754
- 1,5-PENTANEDIAMINE, N1-(TRICYCLO[3.3.1.13,7]DEC-1-YLMETHYL)-, HYDROBROMIDE
- CS-975
- AOB5933
- IEM1754 DIHYDROBROMIDE;IEM1754 2 HBR; AOB5933;
- IEM 1754 dihydrobroMide USP/EP/BP
- N1-((3r,5r,7r)-Adamantan-1-ylmethyl)pentane-1,5-diamine hydrobromide
- 1,5-Pentanediamine, N1-(tricyclo[3.3.1.13,7]dec-1-ylmethyl)-, hydrobromide (1:2)
- IEM 1754 2HBr
- N-(Tricyclo[3.3.1.1(3,7)]dec-1-ylmethyl)-1,5-pentanediamine dihydrobromide
- IEM1754
- IEM 1754 DIHYDROBROMIDE