| 货号 | 规格 | 价格 | 上海 | 北京 | 武汉 | 南京 | 购买数量 |
|---|---|---|---|---|---|---|---|
S88793-2mg |
≥98% | ￥400.00 | 货期：2-3天 | - | - | - |
|
S88793-5mg |
≥98% | ￥700.00 | 货期：2-3天 | - | - | - |
|
S88793-10mg |
≥98% | ￥1200.00 | 货期：2-3天 | - | - | - |
|
S88793-25mg |
≥98% | ￥2400.00 | 货期：2-3天 | - | - | - |
|
S88793-50mg |
≥98% | ￥3500.00 | 货期：2-3天 | - | - | - |
|
S88793-100mg |
≥98% | ￥5000.00 | 货期：2-3天 | - | - | - |
|
Tebanicline (ABT-594, Ebanicline) acts as a partial agonist at neuronal nicotinic acetylcholine receptors, binding to both the α3β4 and the α4β2 subtypes. Tebanicline is an effective synthetic nicotinic (non-opioid) analgesic drug developed by Abbott. It was developed as a less toxic analog of the potent poison dart frog-derived compound epibatidine, which is some 200x stronger than morphine as an analgesic but produces extremely dangerous toxic side effects. Like epibatidine, Tebanicline showed potent analgesic activity against neuropathic pain in both animal and human trials, but with far less toxicity than its parent compound.
| 产品描述： | Tebanicline (ABT-594, Ebanicline) acts as a partial agonist at neuronal nicotinic acetylcholine receptors, binding to both the α3β4 and the α4β2 subtypes. Tebanicline is an effective synthetic nicotinic (non-opioid) analgesic drug developed by Abbott. It was developed as a less toxic analog of the potent poison dart frog-derived compound epibatidine, which is some 200x stronger than morphine as an analgesic but produces extremely dangerous toxic side effects. Like epibatidine, Tebanicline showed potent analgesic activity against neuropathic pain in both animal and human trials, but with far less toxicity than its parent compound. | ||||||||||||||||||||
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| 靶点： | AChR | ||||||||||||||||||||
| 参考文献： | 1. Nirogi R. et al. Eur J Pharmacol. 2011 Oct 1;668(1-2):155-62. 2. Hayashi T, et al.Neurosci Lett. 2016 Dec 7;638:46-50. | ||||||||||||||||||||
| 溶解性： | Soluble in DMSO | ||||||||||||||||||||
| 保存条件： | -20℃ | ||||||||||||||||||||
| 配置溶液浓度参考： |
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| 注意： | 部分产品我司仅能提供部分信息，我司不保证所提供信息的权威性，仅供客户参考交流研究之用。 |
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