Bistramide D and K were extracted from a New Caledonian marine colonia
l ascidian Lissoclinum bistratum and tested against Plasmodium berghei
and P. vinckei petteri in mice. Bistramide D was able to reduce paras
itaemia by almost 50% in P. berghei infected mice, but the ID50 (>5 mg
/kg) was very close to the LD50 (8 mg/kg). In the same assay, bistrami
de K was less active than bistramide D. The mid-term trophozoite and t
he old trophozoite were shown to be the stages most sensitive to bistr
amide D in P. vinckei petteri infected mice. Therefore, bistramides ar
e interesting experimental tools but do not present a major interest a
s potential antimalarial drugs.