Synthesis and Antimalarial Activity of 3,3-Spiroanellated 5,6-Disubstituted 1,2,4-Trioxanes

被引:21
作者
Maurya, Ranjani [1 ]
Soni, Awakash [2 ]
Anand, Devireddy [1 ]
Ravi, Makthala [1 ]
Raju, Kanumuri S. R. [3 ]
Taneja, Isha [3 ]
Naikade, Niraj K. [1 ]
Puri, S. K. [2 ]
Wahajuddin [3 ]
Kanojiya, Sanjeev [4 ]
Yadav, Prem P. [1 ]
机构
[1] Cent Drug Res Inst, Div Med & Proc Chem, Lucknow 226001, Uttar Pradesh, India
[2] Cent Drug Res Inst, Div Parasitol, Lucknow 226001, Uttar Pradesh, India
[3] Cent Drug Res Inst, Div Pharmacokinet & Metab, Lucknow 226001, Uttar Pradesh, India
[4] Cent Drug Res Inst, Sophisticated Analyt Instrument Facil, Lucknow 226001, Uttar Pradesh, India
关键词
1,2,4-trioxane; antimalarial; in vivo; orally active; CHLOROQUINE-RESISTANT PARASITES; RODENT MALARIA; QINGHAOSU ARTEMISININ; PLASMODIUM-BERGHEI; ALLYLIC ALCOHOLS; DRUG; CHEMOTHERAPY; PEROXIDES; CHEMISTRY; YOELII;
D O I
10.1021/ml300188t
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Novel 3,3-spiroanellated 5-aryl, 6-arylvinyl-substituted 1,2,4-trioxanes 19-34 have been synthesized and appraised for their antimalarial activity against multidrug-resistant Plasmodium yoelii nigeriensis in Swiss mice by oral route at doses ranging from 96 mg/kg x 4 days to 24 mg/kg x 4 days. The most active compound of the series (compound 25) provided 100% protection at 24 mg/kg x 4 days, and other 1,2,4-trioxanes 22, 26, 27, and 30 also showed promising activity. In this model, beta-arteether provided 100 and 20% protection at 48 mg/kg x 4 days and 24 mg/kg x 4 days, respectively, by oral route. Compound 25 displayed a similar in vitro pharmacokinetic profile to that of reference drug beta-arteether. The activity results demonstrated the importance of an aryl moiety at the C-5 position on the 1,2,4-trioxane pharmacophore.
引用
收藏
页码:165 / 169
页数:5
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