| Literature DB >> 32390431 |
Papireddy Kancharla1, Rozalia A Dodean2, Yuexin Li2, Sovitj Pou2, Brandon Pybus3, Victor Melendez3, Lisa Read3, Charles E Bane3, Brian Vesely3, Mara Kreishman-Deitrick3, Chad Black3, Qigui Li3, Richard J Sciotti3, Raul Olmeda3, Thu-Lan Luong3, Heather Gaona3, Brittney Potter3, Jason Sousa3, Sean Marcsisin3, Diana Caridha3, Lisa Xie3, Chau Vuong3, Qiang Zeng3, Jing Zhang3, Ping Zhang3, Hsiuling Lin3, Kirk Butler3, Norma Roncal3, Lacy Gaynor-Ohnstad3, Susan E Leed3, Christina Nolan3, Frida G Ceja4, Stephanie A Rasmussen4, Patrick K Tumwebaze5, Philip J Rosenthal6, Jianbing Mu7, Brett R Bayles4,8, Roland A Cooper4, Kevin A Reynolds1, Martin J Smilkstein2, Michael K Riscoe1,2, Jane X Kelly1,2.
Abstract
The global impact of malaria remains staggering despite extensive efforts to eradicate the disease. With increasing drug resistance and the absence of a clinically available vaccine, there is an urgent need for novel, affordable, and safe drugs for prevention and treatment of malaria. Previously, we described a novel antimalarial acridone chemotype that is potent against both blood-stage and liver-stage malaria parasites. Here, we describe an optimization process that has produced a second-generation acridone series with significant improvements in efficacy, metabolic stability, pharmacokinetics, and safety profiles. These findings highlight the therapeutic potential of dual-stage targeting acridones as novel drug candidates for further preclinical development.Entities:
Year: 2020 PMID: 32390431 DOI: 10.1021/acs.jmedchem.0c00539
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446