| CAS: | 36945-98-9 | ||||
| 分子式: | C16H13N3O4 | ||||
| 分子量: | 311.29 | ||||
| 英文名称: |
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| 用途: | Icilin是TRPM8离子通道激动剂。 |
| 货号 | 品牌 | 产品名称 | 规格 | 包装、参考价格 | 详情 | ||||||||||||||||||||||||||||||||||||||
| I860880 | MACKLIN | Icilin,AG-3-5 | >96% | 302元/10mg; | 展开 | ||||||||||||||||||||||||||||||||||||||
储存:-20℃ 状态:浅黄色到黄色固体 折射率:light yellow solid | |||||||||||||||||||||||||||||||||||||||||||
| I9532 | Sigma-Aldrich | Icilin | ≥97% (HPLC), solid | 2021.88元/10 MG; 7297.82元/50 MG; | 展开 | ||||||||||||||||||||||||||||||||||||||
产品说明 一般描述 Icilin is a synthetic cooling agent and modulates human transient receptor potential cation channel (TRPA1). Icilin inhibits transient receptor potential cation channel subfamily M member 8 (TRPM8) and modulates calcium release. Icilin also suppresses transient receptor potential vanilloid subtype 3 (TRPV3). 应用 Icilin has been used as cooling agent in anterior ventromedial preoptic area (VMPO) neurons. 包装 10, 50 mg in glass bottle 生化/生理作用 Icilin is a potent agonist at the CMR1 cold- and menthol-sensitive receptor. 基本信息
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| 375702 | Fluorochem | 3-(2-Hydroxyphenyl)-6-(3-nitrophenyl)-3,4-dihydropyrimidin-2(1H)-one | 95% | 12386元/1g; | 展开 | ||||||||||||||||||||||||||||||||||||||
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