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A 1070722

    
98%

A 1070722

源葉(MedMol)
T72905 一鍵復制產品信息
1384424-80-9
C17H13F3N4O2
362.3059296
1-(7-Methoxyquinolin-4-yl)-3-[6-(trifluoromethyl)pyridin-2-yl]urea
貨號 規格 價格 上海 北京 武漢 南京 購買數量
T72905-5mg 98% ¥290.00 6 - - -
T72905-10mg 98% ¥530.00 7 - - -
T72905-25mg 98% ¥1060.00 6 - - -
T72905-100mg 98% ¥2810.00 貨期:2-3天 - - -
產品介紹 參考文獻 質檢證書(COA) 摩爾濃度計算器 相關產品

產品介紹

A 1070722 is a potent and selective GSK-3 inhibitor, shows high affinity GSK-3α(Ki = 0.6 nM) and GSK-3β(Ki = 0.6 nM). It can penetrate the blood-brain barrier (BBB) and accumulates in brain regions, thus potential for PET radiotracer for the quantification of GSK-3 in brain

產品描述: A 1070722 is a potent and selective GSK-3 inhibitor, shows high affinity GSK-3α(Ki = 0.6 nM) and GSK-3β(Ki = 0.6 nM). It can penetrate the blood-brain barrier (BBB) and accumulates in brain regions, thus potential for PET radiotracer for the quantification of GSK-3 in brain
靶點: GSK-3α:0.6 nM (ki), GSK-3β:0.6 nM (ki);GSK-3
體內研究: PET imaging experiments in anesthetized vervet/African green monkey exhibited that A 1070722 penetrated the blood-brain barrier (BBB) and accumulated in brain regions, with highest radioactivity binding in frontal cortex followed by parietal cortex and anterior cingulate, and with the lowest bindings found in caudate, putamen, and thalamus, similarly to the known distribution of GSK-3 in human brain
參考文獻: 1. Prabhakaran J, et al. Radiosynthesis and in Vivo Evaluation of [11C]A1070722, a High Affinity GSK-3 PET Tracer in Primate Brain. ACS Chem Neurosci. 2017 Aug 16;8(8):1697-1703.
溶解性: Soluble  in  DMSO
保存條件: 2-8°C
配置溶液濃度參考:
1mg 5mg 10mg
1 mM 2.76 ml 13.8 ml 27.601 ml
5 mM 0.552 ml 2.76 ml 5.52 ml
10 mM 0.276 ml 1.38 ml 2.76 ml
50 mM 0.055 ml 0.276 ml 0.552 ml
注意: 部分產品我司僅能提供部分信息,我司不保證所提供信息的權威性,僅供客戶參考交流研究之用。

參考文獻

質檢證書(COA)

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批號:JS298415 貨號:S20001-25g
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摩爾濃度計算器

質量 (mg) = 濃度 (mM) x 體積 (mL) x 分子摩爾量 (g/mol)

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