In the fight against malaria, chemotherapy using bisacridines may represent
an alternative method to overcoming chloroquine-resistance. Eight bis(9-am
ino-6-chloro-2-methoxyacridines), in which acridine moieties were linked by
polyamines substituted with a side chain, were tested for their in-vivo ac
tivity upon mice infected by Plasmodium berghei. Three of the compounds rev
ealed antimalarial activity but no relationship could be deduced from a com
parison of in-vitro and in-vivo activities. N-alkylation of the central ami
no group generated toxicity and, therefore, only compounds N-acylated in th
is position can be selected as leads.