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Journal of medicinal chemistry · 2014

N-aryl-2-aminobenzimidazoles: novel, efficacious, antimalarial lead compounds.

СтатьяПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод пока не подготовлен
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Ramachandran Sreekanth, Hameed P Shahul, Srivastava Abhishek, Shanbhag Gajanan, Morayya Sapna, Rautela Nikhil, Awasthy Disha, Kavanagh Stefan, Bharath Sowmya, Reddy Jitendar, Panduga Vijender, Prabhakar K R, Saralaya Ramanatha, Nanduri Robert, Raichurkar Anandkumar, Menasinakai Sreenivasaiah, Achar Vijayashree, Jiménez-Díaz María Belén, Martínez María Santos, Angulo-Barturen Iñigo, Ferrer Santiago, Sanz Laura María, Gamo Francisco Javier, Duffy Sandra, Avery Vicky M, Waterson David, Lee Marcus C S, Coburn-Flynn Olivia, Fidock David A, Iyer Pravin S, Narayanan Shridhar, Hosagrahara Vinayak, Sambandamurthy Vasan K

Аннотация

From the phenotypic screening of the AstraZeneca corporate compound collection, N-aryl-2-aminobenzimidazoles have emerged as novel hits against the asexual blood stage of Plasmodium falciparum (Pf). Medicinal chemistry optimization of the potency against Pf and ADME properties resulted in the identification of 12 as a lead molecule. Compound 12 was efficacious in the P. berghei (Pb) model of malaria. This compound displayed an excellent pharmacokinetic profile with a long half-life (19 h) in rat blood. This profile led to an extended survival of animals for over 30 days following a dose of 50 mg/kg in the Pb malaria model. Compound 12 retains its potency against a panel of Pf isolates with known mechanisms of resistance. The fast killing observed in the in vitro parasite reduction ratio (PRR) assay coupled with the extended survival highlights the promise of this novel chemical class for the treatment of malaria.

Предметные рубрики MeSH

ИП Урсолов Владлен Сергеевич

ИНН 500118482352 · ОГРНИП 314500117700049

Реквизиты и контакты