6-氨基吲哚
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分子式 C8H8N2 分子量54.938 Beilstein号 22(3/4)4297 EC号 MDL号 MFCD02093959 PubChem编号 属性 沸点 166°C/2.3mmHg 熔点 75-79°C 敏感性 对热敏感;对空气敏
| 货号 | CAS号 | 价格 | 操作 |
|---|---|---|---|
| A119320-1g | 5318-27-4 | ￥428.00 | 询底价 |
| A119320-250mg | 5318-27-4 | ￥239.00 | 询底价 |
| A119320-25g | 5318-27-4 | ￥6,159.00 | 询底价 |
| A119320-5g | 5318-27-4 | ￥1,758.00 | 询底价 |
耗材描述
- 分子式 C8H8N2
- 分子量54.938
- Beilstein号 22(3/4)4297
- EC号
- MDL号 MFCD02093959
- PubChem编号
属性
| 沸点 | 166°C/2.3mmHg |
| 熔点 | 75-79°C |
| 敏感性 | 对热敏感;对空气敏感;对光敏感 |
| 存贮条件 | 储存温度 -20°C;充氩保存 |
描述
| 应用 |
Reactant for preparation of: · Inhibitors of mammalian target of rapamycin (mTOR ) protein · Inhibitors of the AcrAB-TolC efflux pump · Inhibitors of Gli1-mediated transcription in the Hedgehog pathway · Potent DNA-topoisomerase II poisons and anti-MDR agents · Protein kinase C θ (PKCθ) inhibitors · Piperidine carboxamide as transient receptor potential cation channel subfamily V member 1 (TRPV1) antagonists · Potent and selective blockers of the Nav1.8 sodium channel as potential analgesics for the treatment of neuropathic and inflammatory pain · 5,6-fused heteroaromatic ureas as TRPV1 antagonists · Allosteric enhancers of the A3 adenosine receptor · Human liver glycogen phosphorylase (HLGP) inhibitors for the treatment of type 2 diabetes |
| 别名 | ;6-Indolamine;Indol-6-ylamine, NSC 82379 |
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