Kapadia G J, Azuine M A, Balasubramanian V, Sridhar R
Laboratory of Natural Drug Products, Department of Pharmaceutical Sciences, School of Pharmacy, Howard University, 2300 4th Street, NW, Washington, DC 20059, USA.
Pharmacol Res. 2001 Apr;43(4):363-7. doi: 10.1006/phrs.2000.0791.
Malaria is a major tropical disease, which kills two million people annually. The population at risk from this disease has increased because of the difficulties in eradicating the mosquito vector in the endemic regions and the emergence and spread of parasite resistance to all the commonly used antimalarials. Since antimalarials are the major arsenal for treatment of the disease, there is an urgent need for newer drugs with novel mechanisms of action, which will be effective against all strains of the parasite. As a part of our anti-infective drug discovery program, we have investigated 18 compounds including several synthetic and natural naphthoquinones as potential antimalarial agents. We have identified aminonaphthoquinones, as a class of antimalarial compounds with antimalarial activity against Plasmodium falciparum. Among these compounds, 2-amino-3-chloro-1,4-naphthoquinone is the most potent. It had an IC(50)of 0.18 micro M (37.3 ng ml(-1)) against the W2 clone, and is more potent than chloroquine, which had an IC(50)of 0.23 micro M (72 ng ml(-1)). It was also active against the D6 clone. In general, 2-amino-1,4-naphthoquinone analogs and the 4-amino-1,2-napthoquinone analog showed promising antimalarial activity in the bioassay. In contrast, a number of 2-hydroxy-1,4-naphthoquinones and dimeric quinones were less active.
疟疾是一种主要的热带疾病,每年导致200万人死亡。由于在流行地区根除蚊媒存在困难,以及疟原虫对所有常用抗疟药产生耐药性并出现传播,面临这种疾病风险的人口有所增加。由于抗疟药是治疗该疾病的主要武器,因此迫切需要具有新作用机制的新药,这些新药应对所有疟原虫菌株均有效。作为我们抗感染药物发现计划的一部分,我们研究了18种化合物,包括几种合成和天然萘醌作为潜在的抗疟药。我们已确定氨基萘醌是一类对恶性疟原虫具有抗疟活性的抗疟化合物。在这些化合物中,2-氨基-3-氯-1,4-萘醌最为有效。它对W2克隆的IC50为0.18微摩尔(37.3纳克/毫升),比氯喹更有效,氯喹的IC50为0.23微摩尔(72纳克/毫升)。它对D6克隆也有活性。一般来说,2-氨基-1,4-萘醌类似物和4-氨基-1,2-萘醌类似物在生物测定中显示出有前景的抗疟活性。相比之下,一些2-羟基-1,4-萘醌和二聚醌活性较低。