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Mirogabalin

    
99%

Mirogabalin

源叶(MedMol)
S82079 一键复制产品信息
1138245-13-2
C12H19NO2
209.2848
UNII-S7LK2KDM5U; Mirogabalin;
货号 规格 价格 上海 北京 武汉 南京 购买数量
S82079-1mg 99% ¥220.00 >10 - - -
S82079-5mg 99% ¥560.00 >10 - - -
S82079-10mg 99% ¥840.00 >10 - - -
S82079-25mg 99% ¥1000.00 >10 - - -
S82079-50mg 99% ¥1650.00 >10 - - -
S82079-100mg 99% ¥2660.00 >10 - - -
产品介绍 参考文献 质检证书(COA) 摩尔浓度计算器 相关产品

产品介绍

Mirogabalin (DS-5565) is a novel, preferentially selective α2δ-1 ligand characterized by high potency and selectivity to the α2δ-1 subunit of voltage-sensitive calcium channel complexes in the CNS.

产品描述: Mirogabalin (DS-5565) is a novel, preferentially selective α2δ-1 ligand characterized by high potency and selectivity to the α2δ-1 subunit of voltage-sensitive calcium channel complexes in the CNS.
靶点: α2δ-1 Calcium Channel;CalciumChannel
体外研究: Mirogabalin (DS-5565) is a novel, preferentially selective α2δ-1 ligand characterized by high potency and selectivity to the α2δ-1 subunit of voltage-sensitive calcium-channel complexes in the central nervous system (CNS). In vitro experiments using membrane preparations from human and rat α2δ subunit-expressed cells show that Mirogabalin had a slower dissociation rate from α2δ-1 than α2δ-2, in particular, α2δ-1 compared with Pregabalin. Additionally, Mirogabalin shows potent, sustained analgesic effects in streptozotocin-induced diabetic rats with induces pain, and the superior analgesic effects and wider CNS safety margin relative to Pregabalin are attributed to its selectivity for and slow dissociation from α2δ-1 compared with Pregabalin. Mirogabalin (DS-5565) is an α2δ-1 ligand being developed for pain associated with diabetic peripheral neuropathy, fibromyalgia, and postherpetic neuralgia. Mirogabalin targets α2δ-1, an auxiliary protein associated with voltage-sensitive calcium channel complexes in the central nervous system. This binding reduces calcium influx at nerve terminals, therefore reducing the release of several pain neurotransmitters. The ED50 (on the transformed scale) for Mirogabalin is estimated to be 20.5 mg with a 90% confidence interval (CI) of 10.1-41.7 mg
体内研究: Additionally, Mirogabalin shows potent, sustained analgesic effects in streptozotocin-induced diabetic rats with induced pain, and the superior analgesic effects and wider central nervous system (CNS) safety margin relative to Pregabalin are attributed to its selectivity for and slow dissociation from α2δ-1 compared with Pregabalin
参考文献: 1. Vinik A, et al. Efficacy and safety of Mirogabalin (DS-5565) for the treatment of diabetic peripheral neuropathic pain: a randomized, double-blind, placebo- and active comparator-controlled, adaptive proof-of-concept phase 2 study. Diabetes Care. 2014 Dec;37(12):3253-61. 2. Hutmacher MM, et al. Exposure-response modeling of average daily pain score, and dizziness and somnolence, forMirogabalin (DS-5565) in patients with diabetic peripheral neuropathic pain. J Clin Pharmacol. 2016 Jan;56(1):67-77.
溶解性: Soluble  in  H2O
保存条件: -20℃
配置溶液浓度参考:
1mg 5mg 10mg
1 mM 4.778 ml 23.891 ml 47.782 ml
5 mM 0.956 ml 4.778 ml 9.556 ml
10 mM 0.478 ml 2.389 ml 4.778 ml
50 mM 0.096 ml 0.478 ml 0.956 ml
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参考文献

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