| Literature DB >> 24900219 |
Jian-Feng Ge1, Chika Arai2, Mei Yang2, Abu Bakar Md2, Jun Lu2, Nasser S M Ismail3, Sergio Wittlin4, Marcel Kaiser4, Reto Brun4, Susan A Charman5, Tien Nguyen5, Julia Morizzi5, Isamu Itoh6, Masataka Ihara2.
Abstract
Malaria is a serious infectious disease caused by protozoan parasites in tropical and subtropical regions. Even inhabitants of temperate zones are exposed to the danger of malaria infection because of travel and global warming. Novel, effective, safe, and inexpensive drugs are required to treat malaria and contribute to the global goal of eradication. A search for new antimalarial agents has been performed by the synthesis of new benzo[a]phenoxazines, followed by biological evaluations. The derivative SSJ-183 (5), having a 4-aminopyridine group, showed an IC50 value against Plasmodium falciparum of 7.6 nM and a selectivity index of >7300. Cure was achieved by three oral doses of 5 at 100 mg/kg to mice infected with the Plasmodium berghei ANKA strain. The safety of 5 was supported by acute toxicity testing in mice with single doses up to 2000 mg/kg po, chromosome aberration test, in vitro as well as in vivo micronucleus tests, and phototoxicity studies in mice. Thus, 5 is a promising candidate as a new antimalarial agent.Entities:
Keywords: Antimalarial activity; Plasmodium berghei; Plasmodium falciparum; benzo[a]phenoxazine; oral administration
Year: 2010 PMID: 24900219 PMCID: PMC4007839 DOI: 10.1021/ml100120a
Source DB: PubMed Journal: ACS Med Chem Lett ISSN: 1948-5875 Impact factor: 4.345