Basic information Safety Supplier Related

Amodiaquine-d10

Basic information Safety Supplier Related

Amodiaquine-d10 Basic information

Product Name:
Amodiaquine-d10
Synonyms:
  • NSC 13453-10
  • Phenol, 4-[(7-chloro-4-quinolinyl)aMino]-2-[(diethylaMino-d10)Methyl]-
  • 4-[(7-Chloro-4-quinolyl)aMino]-α-(diethylaMino-d10)-o-cresol
  • CaMochin-d10
  • CaMoquinal-d10
  • CaMoquin-d10
  • CaMoquine-d10
  • Flavoquine-d10
CAS:
1189449-70-4
MF:
C20H22ClN3O
MW:
355.86118
Product Categories:
  • Amines
  • Aromatics
  • Heterocycles
  • Intermediates & Fine Chemicals
  • Isotope Labelled Compounds
  • Pharmaceuticals
Mol File:
1189449-70-4.mol
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Amodiaquine-d10 Chemical Properties

Melting point:
194-198°C
storage temp. 
-20°C Freezer
solubility 
Chloroform (Slightly), Methanol (Slightly)
form 
Solid
color 
Pale Yellow to Light Yellow
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Amodiaquine-d10 Usage And Synthesis

Description

Amodiaquine-d10 is intended for use as an internal standard for the quantification of amodiaquine by GC- or LC-MS. Amodiaquine is a prodrug form of the antimalarial compound N-desethyl amodiaquine . It is active against several strains of P. falciparum in vitro (EC50s = 0.23-0.52 nM) and exhibits a synergistic effect when used in combination with N-desethyl amodiaquine. Amodiaquine dose-dependently inhibits development of parasitemia in a mouse model of P. berghei infection.

Chemical Properties

Pale Yellow Solid

Uses

An antimalarial.

IC 50

Plasmodium

References

[1] S T MARIGA. Synergism between amodiaquine and its major metabolite, desethylamodiaquine, against Plasmodium falciparum in vitro.[J]. Antimicrobial Agents and Chemotherapy, 2004, 48 11: 4089-4096. DOI: 10.1128/aac.48.11.4089-4096.2004
[2] JULIANA M Sá T E W Jason L Chong. Malaria drug resistance: new observations and developments.[J]. Essays in biochemistry, 2011, 51: 137-160. DOI: 10.1042/bse0510137
[3] R. JACOBS W C D Alling. AN EVALUATION OF ANTIMALARIAL COMBINATIONS AGAINST PLASMODIUM BERGHEI IN THE MOUSE.[J]. Kisaengch’unghak chapchi. The Korean journal of parasitology, 1963, 11 1: 920-925. DOI: 10.2307/3275719

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