货号:A494835 同义名: Neurotoxin DSP 4 hydrochloride;Neurotoxin DSP 4 (hydrochloride)
DSP-4 showed neurotoxic effects on noradrenergic neurons of adult and developing rats.
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产品名称 | Adrenergic Receptor ↓ ↑ | α-adrenergic receptor ↓ ↑ | β-adrenergic receptor ↓ ↑ | 其他靶点 | 纯度 | ||||||||||||||
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Ivabradine HCl | ✔ | {[allProObj[0].p_purity_real_show]} | |||||||||||||||||
Maprotiline hydrochloride | ✔ | {[allProObj[0].p_purity_real_show]} | |||||||||||||||||
Cisatracurium besylate | ✔ | {[allProObj[0].p_purity_real_show]} | |||||||||||||||||
Yohimbine HCI | ✔ | {[allProObj[0].p_purity_real_show]} | |||||||||||||||||
BMY 7378 |
++
α2C-adrenoceptor, pKi: 6.54 α1D-adrenoceptor, pKi: 5.1 |
+
β1-adrenoceptor, pIC50: 5.1 |
{[allProObj[0].p_purity_real_show]} | ||||||||||||||||
Asenapine maleate |
++++
α2B-adrenergic receptor, pKi: 8.9 α2A-adrenergic receptor, pKi: 8.9 |
{[allProObj[0].p_purity_real_show]} | |||||||||||||||||
Piribedil |
++
adrenoceptor α2C, pKi: 7.2 adrenoceptor α2A, pKi: 7.1 |
{[allProObj[0].p_purity_real_show]} | |||||||||||||||||
Prazosin HCl | ✔ | {[allProObj[0].p_purity_real_show]} | |||||||||||||||||
Silodosin | ✔ | {[allProObj[0].p_purity_real_show]} | |||||||||||||||||
Phenoxybenzamine HCl | ✔ | {[allProObj[0].p_purity_real_show]} | |||||||||||||||||
Naftopidil |
+++
α1D-adrenergic receptor, Ki: 20 nM α1A-adrenergic receptor, Ki: 3.7 nM |
{[allProObj[0].p_purity_real_show]} | |||||||||||||||||
Naftopidil 2HCl |
+
α1-adrenergic receptor, IC50: 0.2 μM |
{[allProObj[0].p_purity_real_show]} | |||||||||||||||||
Alfuzosin HCl | ✔ | {[allProObj[0].p_purity_real_show]} | |||||||||||||||||
Terazosin HCl | ✔ | {[allProObj[0].p_purity_real_show]} | |||||||||||||||||
Atipamezole | ✔ | {[allProObj[0].p_purity_real_show]} | |||||||||||||||||
Phentolamine methanesulfonate salt | ✔ | {[allProObj[0].p_purity_real_show]} | |||||||||||||||||
Doxazosin mesylate | ✔ | {[allProObj[0].p_purity_real_show]} | |||||||||||||||||
Tolazoline HCl | ✔ | {[allProObj[0].p_purity_real_show]} | |||||||||||||||||
Zenidolol hydrochloride |
++++
β2-adrenergic receptor, Ki: 0.7nM β1-adrenergic receptor, Ki: 611nM |
{[allProObj[0].p_purity_real_show]} | |||||||||||||||||
1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。 |
描述 | DSP-4 HCl is a highly selective adrenergic neurotoxin.DSP-4 HCl crosses the blood-brain barrier.DSP-4 HCl can be used to transiently and selectively degrade central and peripheral noradrenergic neurons[1][2] . |
Animal study | DSP-4 HCl administered intravenously to rats at a dose of 50 mg/kg in a single dose destroys LC neurons and fibres[1][2]. |
计算器 | ||||
存储液制备 | 1mg | 5mg | 10mg | |
1 mM 5 mM 10 mM |
3.19mL 0.64mL 0.32mL |
15.97mL 3.19mL 1.60mL |
31.94mL 6.39mL 3.19mL |
CAS号 | 40616-75-9 |
分子式 | C11H16BrCl2N |
分子量 | 313.061 |
别名 | Neurotoxin DSP 4 hydrochloride;Neurotoxin DSP 4 (hydrochloride);DSP-4;DSP-4 hydrochloride |
运输 | 蓝冰 |
存储条件 |
粉末 Inert atmosphere,Room Temperature 液体 -20°C:3-6个月-80°C:12个月 |
溶解度 |
DMSO: 120 mg/mL(383.31 mM),配合低频超声助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO H2O: 50 mg/mL(159.71 mM),配合低频超声助溶 |
动物实验配方 |