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6-Hydroxydopamine Hydrochloride 98%

6-Hydroxydopamine Hydrochloride

源叶(MedMol)
S88807
28094-15-7
C8H12ClNO3
205.64
6-羟基多巴胺盐酸盐;2,4,5-三羟基苯乙胺盐酸盐;2,5-二羟基酪胺盐酸盐;6-羟基多巴胺盐酸盐;盐酸-2,4,5-三羟基苯乙胺;盐酸-6-羟基多巴胺;6-羟基多巴胺(H4381);6-羟基多巴胺合氯化氢;5-(2-氨基乙基)-1,2,4-苯三酚盐酸盐;6-Ohda;6-Hydroxydopamine Hydrochloride;2,4,5-Trihydroxyphenethylamine H
品牌 货号 产品规格 价格(RMB) 库存(上海) 北京 武汉 南京 购买数量
源叶(MedMol) S88807-5mg 98% ¥100.00元 6 - - -
源叶(MedMol) S88807-10mg 98% ¥168.00元 7 - - -
源叶(MedMol) S88807-25mg 98% ¥260.00元 10 - - -
源叶(MedMol) S88807-50mg 98% ¥480.00元 4 - - -
源叶(MedMol) S88807-100mg 98% ¥900.00元 6 - - -
产品介绍 参考文献(2篇) 质检证书(COA) 摩尔浓度计算器 相关产品

产品介绍

Oxidopamine (6-OHDA) hydrochloride is an antagonist of the neurotransmitter dopamine. Oxidopamine hydrochloride is a widely used neurotoxin and selectively destroys dopaminergic neurons. Oxidopamine hydrochloride promotes COX-2 activation, leading to PGE2 synthesis and pro-inflammatory cytokine IL-1β secretion. Oxidopamine hydrochloride can be used for the research of Parkinson’s disease (PD), attention-deficit hyperactivity disorder (ADHD), and Lesch-Nyhan syndrome
产品描述: Oxidopamine (6-OHDA) hydrochloride is an antagonist of the neurotransmitter dopamine. Oxidopamine hydrochloride is a widely used neurotoxin and selectively destroys dopaminergic neurons. Oxidopamine hydrochloride promotes COX-2 activation, leading to PGE2 synthesis and pro-inflammatory cytokine IL-1β secretion. Oxidopamine hydrochloride can be used for the research of Parkinson’s disease (PD), attention-deficit hyperactivity disorder (ADHD), and Lesch-Nyhan syndrome
靶点: COX-2;IL-1β;Caspase-3;Caspase-8;Caspase-9
体内研究: Oxidopamine hydrochloride (5 µg/2 µL, unilaterally injected into the right striatum) induces degeneration of dopaminergic neurons in substantia nigra of rats
参考文献: 1. Kang X, et al. Cyclooxygenase-2 contributes to oxidopamine-mediated neuronal inflammation and injury via the prostaglandin E2 receptor EP2 subtype. Sci Rep. 2017 Aug 25;7(1):9459. 2. Jin F, et al. Neuroprotective effect of resveratrol on 6-OHDA-induced Parkinson's disease in rats. Eur J Pharmacol. 2008 Dec 14;600(1-3):78-82. 3. Fujita H et al. Cell-permeable cAMP analog suppresses 6-hydroxydopamine-induced apoptosis in PC12 cells through the activation of the Akt pathway. Brain Res. 2006 Oct 3;1113(1):10-23. 4. Soto-Otero R et al. Autoxidation and neurotoxicity of 6-hydroxydopamine in the presence of some antioxidants: potential implication in relation to the pathogenesis of Parkinson's disease. J Neurochem. 2000 Apr;74(4):1605-12.
溶解性: Soluble  in  DMSO、H2O
保存条件: -20℃
配置溶液浓度参考:
1mg 5mg 10mg
1 mM 4.863 ml 24.314 ml 48.629 ml
5 mM 0.973 ml 4.863 ml 9.726 ml
10 mM 0.486 ml 2.431 ml 4.863 ml
50 mM 0.097 ml 0.486 ml 0.973 ml
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