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Dihydro Artemisinin (CAS 71939-50-9)

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Alternate Names:
(3R,5aS,6R,8aS,9R,10S,12R,12aR)-Decahydro-3,6,9-trimethyl- 3,12-epoxy-12H-pyrano[4,3-j]-1,2-benzodioxepin-10-ol;β-Dihydroartemisinin; Alaxin; Cotecxin; Cotexin; DHQHS 2; Dihydroartemisinine; Dihydroqinghaosu; USP Artemether Related Compound A
Application:
Dihydro Artemisinin is An active antimalarial metabolite
CAS Number:
71939-50-9
Purity:
≥99%
Molecular Weight:
284.35
Molecular Formula:
C15H24O5
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Dihydro Artemisinin (DHA) is the main metabolite of Artemisinin, a natural product found in the herb Artemisia annua. It is known for its antimalarial activity. Dihydro Artemisinin acts by interfering with the synthesis of cell membrane lipids, which are essential for the growth and survival of the malaria parasite. It also disrupts the cell cycle of the parasite, leading to its death. Dihydro Artemisinin inhibits the enzyme dihydrofolate reductase (DHFR) which is essential for folate synthesis, potentially leading to anemia. Additionally, it suppresses thymidylate synthase which is for DNA synthesis. In vitro studies of Dihydro Artemisinin have been conducted in cell cultures and in isolated organs. These studies have demonstrated that Dihydro Artemisinin is rapidly absorbed and distributed to target organs, with peak concentrations in the plasma occurring within 1 hour of administration. Dihydro Artemisinin is also rapidly metabolized, with the majority of the drug being eliminated within 24 hours. It has shown to be effective against various malaria parasites, such as Plasmodium falciparum, Plasmodium vivax, Plasmodium malariae, and Plasmodium ovale, as well as other protozoan parasites like Leishmania donovani and Trypanosoma brucei.


Dihydro Artemisinin (CAS 71939-50-9) References

  1. Are transporter genes other than the chloroquine resistance locus (pfcrt) and multidrug resistance gene (pfmdr) associated with antimalarial drug resistance?  |  Anderson, TJ., et al. 2005. Antimicrob Agents Chemother. 49: 2180-8. PMID: 15917511
  2. Comparative study of the effectiveness and pharmacokinetics of two rectal artesunate/oral mefloquine combination regimens for the treatment of uncomplicated childhood falciparum malaria.  |  Sirivichayakul, C., et al. 2007. Ann Trop Paediatr. 27: 17-24. PMID: 17469728
  3. Determination of artesunate using reversed-phase HPLC at increased temperature and ELSD detection.  |  Gaudin, K., et al. 2009. J Sep Sci. 32: 231-7. PMID: 19101943
  4. Understanding adherence to reactive treatment of asymptomatic malaria infections in The Gambia.  |  Jaiteh, F., et al. 2021. Sci Rep. 11: 1746. PMID: 33462329
  5. Synergistic integration of dihydro-artemisinin with γ-aminobutyric acid results in a more potential anti-depressant.  |  He, Y., et al. 2021. Bioorg Chem. 110: 104769. PMID: 33677247
  6. Phytochemical analysis and comprehensive evaluation of pharmacological potential of Artemisia brevifolia Wall. ex DC.  |  Tayyaba Batool Kazmi, S., et al. 2022. Saudi Pharm J. 30: 793-814. PMID: 35812152
  7. Clinical pharmacology and therapeutic potential of artemisinin and its derivatives in the treatment of malaria.  |  de Vries, PJ. and Dien, TK. 1996. Drugs. 52: 818-36. PMID: 8957153
  8. In vitro susceptibility of Plasmodium falciparum isolates in Vietnam to artemisinin derivatives and other antimalarials.  |  Wongsrichanalai, C., et al. 1997. Acta Trop. 63: 151-8. PMID: 9088428

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Dihydro Artemisinin, 100 mg

sc-211332
100 mg
$228.00