TY - JOUR
T1 - Synthesis of febrifugine derivatives and development of an effective and safe tetrahydroquinazoline-type antimalarial
AU - Kikuchi, Haruhisa
AU - Horoiwa, Seiko
AU - Kasahara, Ryota
AU - Hariguchi, Norimitsu
AU - Matsumoto, Makoto
AU - Oshima, Yoshiteru
N1 - Funding Information:
This work was supported in part by the SUNBOR GRANT from the Suntory Institute for Bioorganic Research , and Kobayashi International Scholarship Foundation .
PY - 2014/4/9
Y1 - 2014/4/9
N2 - Febrifugine, a quinazoline alkaloid isolated from Dichroa febrifuga roots, shows powerful antimalarial activity against Plasmodium falciparum. Although the use of ferifugine as an antimalarial drug has been precluded because of its severe side effects, its potent antimalarial activity has stimulated medicinal chemists to pursue its derivatives instead, which may provide valuable leads for novel antimalarial drugs. In the present study, we synthesized new derivatives of febrifugine and evaluated their in vitro and in vivo antimalarial activities to develop antimalarials that are more effective and safer. As a result, we proposed tetrahydroquinazoline-type derivative as a safe and effective antimalarial candidate.
AB - Febrifugine, a quinazoline alkaloid isolated from Dichroa febrifuga roots, shows powerful antimalarial activity against Plasmodium falciparum. Although the use of ferifugine as an antimalarial drug has been precluded because of its severe side effects, its potent antimalarial activity has stimulated medicinal chemists to pursue its derivatives instead, which may provide valuable leads for novel antimalarial drugs. In the present study, we synthesized new derivatives of febrifugine and evaluated their in vitro and in vivo antimalarial activities to develop antimalarials that are more effective and safer. As a result, we proposed tetrahydroquinazoline-type derivative as a safe and effective antimalarial candidate.
KW - Antimalarials
KW - Plasmodium falciparum
KW - Quinazoline alkaloids
KW - Structure-activity relationship
UR - http://www.scopus.com/inward/record.url?scp=84896726653&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84896726653&partnerID=8YFLogxK
U2 - 10.1016/j.ejmech.2014.01.036
DO - 10.1016/j.ejmech.2014.01.036
M3 - Article
C2 - 24565569
AN - SCOPUS:84896726653
SN - 0223-5234
VL - 76
SP - 10
EP - 19
JO - European Journal of Medicinal Chemistry
JF - European Journal of Medicinal Chemistry
ER -