N-[(3r)-アダマンタン-1-イル]キノキサリン-2-カルボキサミド

N-[(3r)-アダマンタン-1-イル]キノキサリン-2-カルボキサミド 化学構造式
226878-01-9
CAS番号.
226878-01-9
化学名:
N-[(3r)-アダマンタン-1-イル]キノキサリン-2-カルボキサミド
别名:
N-(トリシクロ[3.3.1.13,7]デカン-1-イル)-2-キノキサリンカルボアミド;N-[(3r)-アダマンタン-1-イル]キノキサリン-2-カルボキサミド
英語名:
NPS 2390
英語别名:
N-(1-adamantyl)quinoxaline-2-carboxamide;N-(Adamantan-1-yl)quinoxaline-2-carboxamide;N-tricyclo[3.3.1.13,7]dec-1-yl-2-quinoxalinecarboxamide;2-Quinoxalinecarboxamide, N-tricyclo[3.3.1.13,7]dec-1-yl-;Inhibitor,NPS2390,Calcium-sensing receptor,NPS-2390,mGluR,inhibit,Metabotropic glutamate receptors,CaSR,NPS 2390
CBNumber:
CB0972884
化学式:
C19H21N3O
分子量:
307.39
MOL File:
226878-01-9.mol

N-[(3r)-アダマンタン-1-イル]キノキサリン-2-カルボキサミド 物理性質

沸点 :
542.4±30.0 °C(Predicted)
比重(密度) :
1.28±0.1 g/cm3(Predicted)
貯蔵温度 :
2-8°C
溶解性:
Soluble to 50 mM in DMSO and to 50 mM in ethanol
外見 :
Powder
酸解離定数(Pka):
11.53±0.20(Predicted)
色:
White to light yellow

安全性情報

N-[(3r)-アダマンタン-1-イル]キノキサリン-2-カルボキサミド 価格 もっと(2)

メーカー 製品番号 製品説明 CAS番号 包装 価格 更新時間 購入
富士フイルム和光純薬株式会社(wako) W01TOC4134
NPS 2390
226878-01-9 10mg ¥66000 2024-03-01 購入
富士フイルム和光純薬株式会社(wako) W01TOC4134
NPS 2390
226878-01-9 50mg ¥279000 2024-03-01 購入

N-[(3r)-アダマンタン-1-イル]キノキサリン-2-カルボキサミド 化学特性,用途語,生産方法

説明

Metabotropic glutamate receptors (mGluRs), mediate excitatory synaptic transmission in the central nervous system. Potent and selective antagonists of the type I mGluRs (mGluR1 and mGluR5) are of interest as novel therapeutics for the treatment of various CNS disorders, such as pain, epilepsy, and stroke. NPS 2390 is a first generation quinoxaline derivative that acts as a noncompetitive antagonist of mGluR1 and mGluR5 with IC50 values equal to 5.2 and 82 nM, respectively). At concentrations up to 30 μM, NPS 2390 does not affect mGluR2 or mGluR8 or a standard collection of 37 additional receptors, ion channels, and enzymes. At a dose of 10 mg/kg, NPS 2390 displaced the specifically bound mGlu1R-selective antagonist, [3H]R214127, in rat cerebellum.

使用

Metabotropic glutamate receptors (mGluRs), mediate excitatory synaptic transmission in the central nervous system. Potent and selective antagonists of the type I mGluRs (mGluR1 and mGluR5) are of interest as novel therapeutics for the treatment of various CNS disorders, such as pain, epilepsy, and stroke. NPS 2390 is a first generation quinoxaline derivative that acts as a noncompetitive antagonist of mGluR1 and mGluR5 with IC50 values equal to 5.2 and 82 nM, respectively). At concentrations up to 30 μM, NPS 2390 does not affect mGluR2 or mGluR8 or a standard collection of 37 additional receptors, ion channels, and enzymes. At a dose of 10 mg/kg, NPS 2390 displaced the specifically bound mGlu1R-selective antagonist, [3H]R214127, in rat cerebellum.

N-[(3r)-アダマンタン-1-イル]キノキサリン-2-カルボキサミド 上流と下流の製品情報

原材料

準備製品


N-[(3r)-アダマンタン-1-イル]キノキサリン-2-カルボキサミド 生産企業

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N-[(3r)-アダマンタン-1-イル]キノキサリン-2-カルボキサミド  スペクトルデータ(1HNMR)



  • 226878-01-9
  • N-tricyclo[3.3.1.13,7]dec-1-yl-2-quinoxalinecarboxamide
  • N-(1-adamantyl)quinoxaline-2-carboxamide
  • N-(Adamantan-1-yl)quinoxaline-2-carboxamide
  • Inhibitor,NPS2390,Calcium-sensing receptor,NPS-2390,mGluR,inhibit,Metabotropic glutamate receptors,CaSR,NPS 2390
  • 2-Quinoxalinecarboxamide, N-tricyclo[3.3.1.13,7]dec-1-yl-
  • N-(トリシクロ[3.3.1.13,7]デカン-1-イル)-2-キノキサリンカルボアミド
  • N-[(3r)-アダマンタン-1-イル]キノキサリン-2-カルボキサミド
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