Artemotil

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Structural formula
Artemoil structure
General
Non-proprietary name Artemotil
other names

(3 R , 5a S , 6 R , 8a S , 9 R , 10 S , 12 R , 12a R ) -Decahydro-10-ethoxy-3,6,9-trimethyl-3,12-epoxy-12 H -pyrano [4,3- j ] -1,2-benzodioxepine ( IUPAC )

Molecular formula C 17 H 28 O 5
External identifiers / databases
CAS number 109716-83-8
PubChem 72416
Wikidata Q72443831
Drug information
ATC code

P01 BE04

Drug class

Antiprotozoic

properties
Molar mass 312.40 g mol −1
safety instructions
Please note the exemption from the labeling requirement for drugs, medical devices, cosmetics, food and animal feed
GHS hazard labeling
no classification available
As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions .

Artemotil (also called arteether, not to be confused with Arte m ether ) is from Artemisinin derived semi-synthetic drug for the treatment of by Plasmodium falciparum causing malaria .

Pharmacological properties

Like all artemisinin derivatives, Artemotil acts via an endogenous peroxide group that presumably forms radicals that are toxic to the plasmodia in infected erythrocytes . Artemotil is given parenterally , which is beneficial in debilitated patients who have problems with feeding. In contrast to other artemisinin derivatives, Artemotil has a long half-life of around 20 hours when injected. Artemotil is metabolized in the liver to dihydroartemisinin , which is just as effective as Artemotil.

Preparations and Uses

Artemotil is approved as a monopreparation Artecef ® in the Netherlands for the emergency treatment of severe malaria cases by intramuscular injection . Artecef ® is produced in doses of 50 mg and 150 mg Artemotil in sesame oil .

As a rule, the World Health Organization advises against the use of artemisinin derivatives as a single substance in order to reduce the risk of developing resistance to artemisinin derivatives. In practice, this is likely to be difficult to implement in emergency therapy. Artemotil is to be regarded as a substitute for the infusion of quinine because, unlike quinine, it should be easier to use and show fewer side effects.

Individual evidence

  1. This substance has either not yet been classified with regard to its hazardousness or a reliable and citable source has not yet been found.
  2. WHO on Artecef approval in the Netherlands ( Memento from June 11, 2008 in the Internet Archive )
  3. Dutch registration for artemotil injections. In: TDR news, October 2000, p. 13 (PDF; 444 kB).