Total synthesis of thiaplakortone A: Derivatives as metabolically stable leads for the treatment of malaria

Rebecca H Pouwer, Sophie M Deydier, Phuc Van Le, Brett D Schwartz, Nicole C Franken, Rohan A Davis, Mark Coster, Susan Ann Charman, Michael D Edstein, Tina S Skinner-Adams, Katherine T Andrews, Ian D Jenkins, Ronald J Quinn

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12 Citations (Scopus)

Abstract

Thiaplakortone A (3a), an antimalarial natural product, was prepared by an operationally simple and scalable synthesis. In our efforts to deliver a lead compound with improved potency, metabolic stability, and selectivity, the synthesis was diverted to access a series of analogues. Compounds 3a-d showed nanomolar activity against the chloroquine-sensitive (3D7) Plasmodium falciparum line and were more active against the chloroquine- and mefloquine-resistant (Dd2) P. falciparum line. All compounds are Rule-of-5 compliant, and we show that metabolic stability can be enhanced via modification at either the primary or pyrrole nitrogen. These promising results lay the foundation for the development of this structurally unprecedented natural product.
Original languageEnglish
Pages (from-to)178 - 182
Number of pages5
JournalACS Medicinal Chemistry Letters
Volume5
Issue number2
DOIs
Publication statusPublished - 2014

Cite this

Pouwer, R. H., Deydier, S. M., Le, P. V., Schwartz, B. D., Franken, N. C., Davis, R. A., ... Quinn, R. J. (2014). Total synthesis of thiaplakortone A: Derivatives as metabolically stable leads for the treatment of malaria. ACS Medicinal Chemistry Letters, 5(2), 178 - 182. https://doi.org/10.1021/ml400447v