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  • (S)-Willardiine ((-)-Willardiine)
(S)-Willardiine ((-)-Willardiine)的可视化放大

(S)-Willardiine ((-)-Willardiine)

(S)-Willardiine ((-)-Willardiine) 是一种有效的 AMPA/红藻氨酸受体激动剂,EC50 为 44.8 uM。

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¥837-3675
价格
670-2940
(S)-Willardiine ((-)-Willardiine)的二维码

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  • 货号: ajce44666
  • CAS: 21416-43-3
  • 别名: 尿嘧啶基丙氨酸; (-)-Willardiine
  • 分子式: C7H9N3O4
  • 分子量: 199.16
  • 纯度: >98%
  • 溶解度: DMSO : < 1 mg/mL (insoluble or slightly soluble)
  • 储存: Store at -20°C
  • 库存: 现货

Background

(S)-Willardiine is a potent agonist of AMPA/kainate receptors with EC50 of 44.8 uM.IC50 value: 44.8 uM(EC50) [1]Target: AMPA/kainate receptor agonistin vitro: The (S)- but not (R)-isomers of willardiine and 5-bromowillardiine were potent agonists, producing rapidly but incompletely desensitizing responses [1]. At a concentration of 1.8 mM, Ca2+ inhibited the currents induced by 100 microM willardiine by approximately 50% [2].in vivo: In newborn mice (P5, histopathology at P10), local injection of the AMPA receptor agonist S-bromo-willardiine at day 5 after birth induced cortical damage and white matter damage, which was reduced in a dose-dependent manner by the AMPA receptor antagonists [3].



[1]. Patneau DK, et al. Activation and desensitization of AMPA/kainate receptors by novel derivatives of willardiine. J Neurosci. 1992 Feb;12(2):595-606. [2]. Fukushima T, et al. Calcium inhibits willardiine-induced responses in kainate receptor GluR6(Q)/KA-2. Neuroreport. 2001 Jan 22;12(1):163-7. [3]. Gressens P, et al. The effects of AMPA receptor antagonists in models of stroke and neurodegeneration. Eur J Pharmacol. 2005 Sep 5;519(1-2):58-67.

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