Objective: To synthesize orally bioavailable artemisinin dimers and the evaluation of their in vivo antimalarial activity. Methods: Artemsisin dimers were synthesized and their antimalarial activity was determined in in vitro and in vivo studies (administered orally and IP). Results: Dimers 5 and 6 provided 100% suppression of parastemia throughout the oral administration study, with all animals surviving up to day 28 (the last day of the study). Conclusion: Dimers 4-7 displayed markedly improved in vitro activity against P. falciparum, while the in vivo activity against P. berghei was highly encouraging, with 5 and 6 completely clearing parasitemia from the start of the drug treatment until the end of the study (day 28)
Thesis (PhD (Pharmaceutical Chemistry))--North-West University, Potchefstroom Campus, 2013Introducti...
In vitro assays and rodent screens In vitro antimalarial activity was assayed by inhibition of uptak...
Novel artemisinin–quinoline hybrid-dimers were synthesized from dihydroartemisinin and different ami...
Malaria, one of the three most important life-threatening infectious diseases, is recommended to be ...
This research describes the use of novel antimalarial combinations of the new artemisinin derivative...
Supplementary data related to this article can be found at http:// dx.doi.org/10.1016/j.ejmech.2014...
Thesis (PhD (Pharmaceutical Chemistry))--North-West University, Potchefstroom Campus, 2013Malaria ha...
Artemisinin, also known as qinghaosu, is a tetracyclic 1,2,4-trioxane occurring in Artemisia annua. ...
Objectives: The in vitro and in vivo efficacy and drug-drug interactions of the novel semi-synthetic...
Objectives The aim of this study was to synthesize a series of ethylene glycol ether derivatives of ...
Artemisinin and its derivatives are renowned for their potent antimalarial activity. They have found...
Three new 5-carbon-linked trioxane dimer carboxylate esters have been prepared from the natural trio...
Ten novel, second-generation, fluorinated ether and ester analogues of the potent firstgeneration an...
The aim of this study was to synthesize a series of ethylene glycol (EG) ethers and quinoline hybrid...
The activities of artemisinin (QHS) and a number of its semi-synthetic analogues, as well as Fenozan...
Thesis (PhD (Pharmaceutical Chemistry))--North-West University, Potchefstroom Campus, 2013Introducti...
In vitro assays and rodent screens In vitro antimalarial activity was assayed by inhibition of uptak...
Novel artemisinin–quinoline hybrid-dimers were synthesized from dihydroartemisinin and different ami...
Malaria, one of the three most important life-threatening infectious diseases, is recommended to be ...
This research describes the use of novel antimalarial combinations of the new artemisinin derivative...
Supplementary data related to this article can be found at http:// dx.doi.org/10.1016/j.ejmech.2014...
Thesis (PhD (Pharmaceutical Chemistry))--North-West University, Potchefstroom Campus, 2013Malaria ha...
Artemisinin, also known as qinghaosu, is a tetracyclic 1,2,4-trioxane occurring in Artemisia annua. ...
Objectives: The in vitro and in vivo efficacy and drug-drug interactions of the novel semi-synthetic...
Objectives The aim of this study was to synthesize a series of ethylene glycol ether derivatives of ...
Artemisinin and its derivatives are renowned for their potent antimalarial activity. They have found...
Three new 5-carbon-linked trioxane dimer carboxylate esters have been prepared from the natural trio...
Ten novel, second-generation, fluorinated ether and ester analogues of the potent firstgeneration an...
The aim of this study was to synthesize a series of ethylene glycol (EG) ethers and quinoline hybrid...
The activities of artemisinin (QHS) and a number of its semi-synthetic analogues, as well as Fenozan...
Thesis (PhD (Pharmaceutical Chemistry))--North-West University, Potchefstroom Campus, 2013Introducti...
In vitro assays and rodent screens In vitro antimalarial activity was assayed by inhibition of uptak...
Novel artemisinin–quinoline hybrid-dimers were synthesized from dihydroartemisinin and different ami...