NPS 2390

NPS 2390 Struktur
226878-01-9
CAS-Nr.
226878-01-9
Englisch Name:
NPS 2390
Synonyma:
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
Summenformel:
C19H21N3O
Molgewicht:
307.39
MOL-Datei:
226878-01-9.mol

NPS 2390 Eigenschaften

Siedepunkt:
542.4±30.0 °C(Predicted)
Dichte
1.28±0.1 g/cm3(Predicted)
storage temp. 
2-8°C
Löslichkeit
Soluble to 50 mM in DMSO and to 50 mM in ethanol
Aggregatzustand
Powder
pka
11.53±0.20(Predicted)

Sicherheit

NPS 2390 Chemische Eigenschaften,Einsatz,Produktion Methoden

Beschreibung

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.

Verwenden

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.

NPS 2390 Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


NPS 2390 Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

Global( 41)Lieferanten
Firmenname Telefon E-Mail Land Produktkatalog Edge Rate
ATK CHEMICAL COMPANY LIMITED
+undefined-21-51877795
ivan@atkchemical.com China 32686 60
Nantong HI-FUTURE Biology Co., Ltd.
+undefined18051384581
sales@chemhifuture.com China 3136 58
TargetMol Chemicals Inc.
+1-781-999-5354
support@targetmol.com United States 19973 58
Wuhan Topule Biopharmaceutical Co., Ltd
+8618327326525
masar@topule.com China 8474 58
Aladdin Scientific
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sales@aladdinsci.com United States 57511 58
Atomic chemistry 0370-2785705 19339619972
2234585634@qq.com China 4175 58
DKMbiochem.Co. Ltd 15901859516
sales@DKMbiochem.com China 344 58
HangZhou YuHao Chemical Technology Co., Ltd. 0571-82693216
info@yuhaochemical.com China 2031 58
EMMX Biotechnology LLC 888-539-0666
info@emmx.com United States 8449 60
ShangHai Biochempartner Co.,Ltd 17754423994 17754423994
2853530910@QQ.com China 8011 62

  • 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-
  • 226878-01-9
  • C19H21ON3
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