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2-Quinoxalinecarboxamide, N-(4-methoxyphenyl)-

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Products Intro: Product Name:5-HT3 antagonist 5
CAS:901599-43-7
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Products Intro: Product Name:5-HT3 antagonist 5
CAS:901599-43-7
Purity:99.41% Package:5mg;63USD|10mg;98USD|25mg;197USD
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Products Intro: Product Name:WAY-327157
CAS:901599-43-7
Purity:98% Package:$309.9/5mg;$515.9/10mg;$1030.9/25mg;$1648.9/50mg;$2644.9/100mg;Bulk package Remarks:98%
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Products Intro: Product Name:5-HT3 antagonist 5
CAS:901599-43-7
Purity:98% HPLC Package:5mg,10mg,50mg,100mg,1g,5g
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Products Intro: Product Name:5-HT3 antagonist 5
CAS:901599-43-7
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2-Quinoxalinecarboxamide, N-(4-methoxyphenyl)- manufacturers

  • 5-HT3 antagonist 5
  • 5-HT3 antagonist 5 pictures
  • $63.00 / 5mg
  • 2024-11-19
  • CAS:901599-43-7
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  • Purity: 99.41%
  • Supply Ability: 10g
2-Quinoxalinecarboxamide, N-(4-methoxyphenyl)- Basic information
Product Name:2-Quinoxalinecarboxamide, N-(4-methoxyphenyl)-
Synonyms:2-Quinoxalinecarboxamide, N-(4-methoxyphenyl)-;WAY-327157;5-HT3 antagonist 5;WAY327157,WAY 327157;N-(4-Methoxyphenyl)quinoxaline-2-carboxamide;N-(4-methoxyphenyl)-2-quinoxalinecarboxamide;5-HT3 antagonist 5, 10 mM in DMSO
CAS:901599-43-7
MF:C16H13N3O2
MW:279.29
EINECS:
Product Categories:
Mol File:901599-43-7.mol
2-Quinoxalinecarboxamide, N-(4-methoxyphenyl)- Structure
2-Quinoxalinecarboxamide, N-(4-methoxyphenyl)- Chemical Properties
Melting point 176-178 °C(Solv: ethanol (64-17-5); ethyl ether (60-29-7))
Boiling point 393.2±32.0 °C(Predicted)
density 1.312±0.06 g/cm3(Predicted)
storage temp. Store at -20°C
solubility DMSO : 20.83 mg/mL (74.58 mM; ultrasonic and warming and heat to 60°C)
pka11.07±0.70(Predicted)
form Solid
color Light yellow to yellow
Safety Information
MSDS Information
2-Quinoxalinecarboxamide, N-(4-methoxyphenyl)- Usage And Synthesis
Uses5-HT3 antagonist 5 is a quinoxalin-2-carboxamide compound, a 5-HT3 receptor antagonist. 5-HT3 antagonist 5 exerts antagonism on 5-HT3 agonist and 2-methyl-5-HT, and shows anti-depressant effect in mice[1].
in vivo

5-HT3 antagonist 5 (compound 4c) (1 mg/kg; i.p.; single dose) decreases the duration of immobility and shows anti-depressant effect in FST mice[1].

Animal Model:Swiss albino mice (23 ± 2 g)[1]
Dosage:1 mg/kg
Administration:Intraperitoneal injection; single dose; locomotor scores tested 10 min after administration
Result:Reduced the duration of immobility as compared to the vehicle-treated (control) group.
Showed no effect on the locomotion of mice as observed in spontaneous locomotor activity.
IC 505-HT3 Receptor
References[1] Mahesh R, et al. Design, synthesis and structure-activity relationship of novel quinoxalin-2-carboxamides as 5-HT3 receptor antagonists for the management of depression. Bioorg Med Chem Lett. 2010 Nov 15;20(22):6773-6. DOI:10.1016/j.bmcl.2010.08.128
2-Quinoxalinecarboxamide, N-(4-methoxyphenyl)- Preparation Products And Raw materials
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