Diversity-Oriented Synthesis Yields a Novel Lead for the Treatment of Malaria.

Diversity-Oriented Synthesis Yields a Novel Lead for the Treatment of Malaria.
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DOI:
10.1021/ml200244k
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发表时间:
2012-02-09
影响因子:
4.2
通讯作者:
Schreiber, Stuart
Schreiber, Stuart
中科院分区:
医学3区
文献类型:
--
作者:
Heidebrecht, Richard W., Jr.;Mulrooney, Carol;Austin, Christopher P.;Barker, Robert H., Jr.;Beaudoin, Jennifer A.;Cheng, Ken Chih-Chien;Comer, Eamon;Dandapani, Sivaraman;Dick, Justin;Duvall, Jeremy R.;Ekland, Eric H.;Fidock, David A.;Fitzgerald, Mark E.;Foley, Michael;Guha, Rajarshi;Hinkson, Paul;Kramer, Martin;Lukens, Amanda K.;Masi, Daniela;Marcaurelle, Lisa A.;Su, Xin-Zhuan;Thomas, Craig J.;Weiwer, Michel;Wiegand, Roger C.;Wirth, Dyann;Xia, Menghang;Yuan, Jing;Zhao, Jinghua;Palmer, Michelle;Munoz, Benito;Schreiber, Stuart

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Here, we describe the discovery of a novel antimalarial agent using phenotypic screening of Plasmodium falciparum asexual blood-stage parasites. Screening a novel compound collection created using diversity-oriented synthesis (DOS) led to the initial hit. Structure–activity relationships guided the synthesis of compounds having improved potency and water solubility, yielding a subnanomolar inhibitor of parasite asexual blood-stage growth. Optimized compound 27 has an excellent off-target activity profile in erythrocyte lysis and HepG2 assays and is stable in human plasma. This compound is available via the molecular libraries probe production centers network (MLPCN) and is designated ML238.
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