In this paper we describe the preparation of some biphenylquinuclidine derivatives and their evaluation as inhibitors of squalene synthase in order to explore their potential in the treatment of the parasitic diseases leishmaniasis and Chagas disease. The compounds were screened against recombinant Leishmania major squalene synthase and against Leishmania mexicana promastigotes, Leishmania donovani intracellular amastigotes and Trypanosoma cruzi intracellular amastigotes. Compounds that inhibited the enzyme, also reduced the levels of steroids and caused growth inhibition of L. mexicana promastigotes. However there was a lower correlation between inhibition of the enzyme and growth inhibition of the intracellular parasites, possibly due to ...
As a part of our project aimed at developing new safe chemotherapeutic agents against tropical disea...
The synthesis and in vitro activity of R(+)-Limonene derivatives against Leishmania and Trypanosoma ...
Sulfonamide and urea derivatives of quinacrine with varying methylene spacer lengths were synthesise...
In this paper we describe the preparation of some biphenylquinuclidine derivatives and their evaluat...
There is an urgent need for the development of new drugs for the treatment of tropical parasitic dis...
This paper concerns the synthesis of various simplified analogues of the novel anti-microbial agent,...
Leishmaniasis is an important disease in widely dispersed regions of the world. In South America, vi...
In this paper we describe the preparation of some biphenylquinuclidine derivatives and their evaluat...
The progresses made in the field of drug design to combat tropical protozoan parasitic diseases, suc...
Currently available drugs being used to treat leishmaniasis have several shortcomings, including hig...
Leishmaniasis is a neglected, parasitic tropical disease caused by an intracellular protozoan from t...
<div><p>Trypanosomatid parasites are the causative agents of many neglected tropical diseases and th...
MSc (Pharmaceutical Chemistry), North-West University, Potchefstroom CampusLeishmaniasis is a diseas...
MSc (Pharmaceutical Chemistry), North-West University, Potchefstroom CampusLeishmaniasis is a vector...
A series of diverse simple C2-aryl quinolines was synthesized de novo via a straightforward synthesi...
As a part of our project aimed at developing new safe chemotherapeutic agents against tropical disea...
The synthesis and in vitro activity of R(+)-Limonene derivatives against Leishmania and Trypanosoma ...
Sulfonamide and urea derivatives of quinacrine with varying methylene spacer lengths were synthesise...
In this paper we describe the preparation of some biphenylquinuclidine derivatives and their evaluat...
There is an urgent need for the development of new drugs for the treatment of tropical parasitic dis...
This paper concerns the synthesis of various simplified analogues of the novel anti-microbial agent,...
Leishmaniasis is an important disease in widely dispersed regions of the world. In South America, vi...
In this paper we describe the preparation of some biphenylquinuclidine derivatives and their evaluat...
The progresses made in the field of drug design to combat tropical protozoan parasitic diseases, suc...
Currently available drugs being used to treat leishmaniasis have several shortcomings, including hig...
Leishmaniasis is a neglected, parasitic tropical disease caused by an intracellular protozoan from t...
<div><p>Trypanosomatid parasites are the causative agents of many neglected tropical diseases and th...
MSc (Pharmaceutical Chemistry), North-West University, Potchefstroom CampusLeishmaniasis is a diseas...
MSc (Pharmaceutical Chemistry), North-West University, Potchefstroom CampusLeishmaniasis is a vector...
A series of diverse simple C2-aryl quinolines was synthesized de novo via a straightforward synthesi...
As a part of our project aimed at developing new safe chemotherapeutic agents against tropical disea...
The synthesis and in vitro activity of R(+)-Limonene derivatives against Leishmania and Trypanosoma ...
Sulfonamide and urea derivatives of quinacrine with varying methylene spacer lengths were synthesise...