Basic information Safety Supplier Related

Artemisinin-d3

Basic information Safety Supplier Related

Artemisinin-d3 Basic information

Product Name:
Artemisinin-d3
Synonyms:
  • (3R,5aS,6R,8aS,9R,12S,12aR)-Octahydro-3,6-dimethyl-9-(methyl-d3)-3,12-epox-12H-pyrano[4,3-j]-1,2-benzodioxepin-10(3H)-one
  • Arteannuin-d3
  • Artemisine-d3
  • Artemisinin-d3
  • Huanghuahaosu-d3
  • QHS-d3
  • [2H3]-Artemisinin
  • 3,12-Epoxy-12H-pyrano[4,3-j]-1,2-benzodioxepin-10(3H)-one, octahydro-3,6-dimethyl-9-(methyl-d3)-, [3R-(3α,5aβ,6β,8aβ,9α,12β,12aR*)]- (9CI)
CAS:
176652-07-6
MF:
C15H22O5
MW:
282.33218
Product Categories:
  • Intermediates & Fine Chemicals
  • Isotope Labeled Compounds
  • Pharmaceuticals
  • Isotope Labelled Compounds
  • Isotope Labelled Compounds, Pharmaceuticals, Intermediates & Fine Chemicals
Mol File:
176652-07-6.mol
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Artemisinin-d3 Chemical Properties

Melting point:
156-157°C
storage temp. 
-20°C Freezer
solubility 
DMSO: Slightly soluble,Methanol: Slightly soluble
form 
A solid
CAS DataBase Reference
176652-07-6
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Artemisinin-d3 Usage And Synthesis

Description

Artemisinin-d3 is intended for use as an internal standard for the quantification of artemisinin . Artemisinin is an endoperoxide antimalarial agent with anticancer activity. It reduces the growth of various P. falciparum strains in vitro (IC50s = 3.98-20.36 nM) and reduces parasitemia in mice infected with P. falciparum with a curative dose (CD50) value of 140 mg/kg. It also reduces P. berghei infection in mice (ED50 = 5.6 mg/kg per day). Artemisinin (100-400 μM) induces cell cycle arrest in the G0/G1 phase and apoptosis and inhibits growth of SK-N-AS, BE(2)-C, SK-N-DZ, and SHEP1 neuroblastoma cells in a time- and concentration-dependent manner. It also suppresses BE(2)-C cell colony formation in a soft agar assay and reduces tumor growth in a BE(2)-C mouse xenograft model. Formulations containing artemisinin have been used in combination therapies for the treatment of malaria.

Chemical Properties

Crystalline Solid

Uses

Active antimalarial constituent of the tradional Chinese medicinal herb Artemisia annua L., Compositae, which has been known for almost 2000 years as Qinghao. Antimalarial

IC 50

Plasmodium

References

[1] MONIQUE AKOACHERE. In vitro assessment of methylene blue on chloroquine-sensitive and -resistant Plasmodium falciparum strains reveals synergistic action with artemisinins.[J]. Antimicrobial Agents and Chemotherapy, 2005: 4592-4597. DOI: 10.1128/aac.49.11.4592-4597.2005
[2] SHUNQIN ZHU. Artemisinin reduces cell proliferation and induces apoptosis in neuroblastoma.[J]. Oncology reports, 2014, 32 3: 1094-1100. DOI: 10.3892/or.2014.3323
[3] ANNE ROBERT. The antimalarial drug artemisinin alkylates heme in infected mice.[J]. Proceedings of the National Academy of Sciences of the United States of America, 2005, 102 38: 13676-13680. DOI: 10.1073/pnas.0500972102
[4] A.N. CHAWIRA. The effect of combinations of qinghaosu (artemisinin) with standard antimalarial drugs in the suppressive treatment of malaria in mice[J]. Transactions of The Royal Society of Tropical Medicine and Hygiene, 1987, 81 4: Pages 554-558. DOI: 10.1016/0035-9203(87)90404-4

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