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Microscale High-Throughput Experimentation as an Enabling Technology in Drug Discovery: Application in the Discovery of (Piperidinyl)pyridinyl-1H-benzimidazole Diacylglycerol Acyltransferase 1 Inhibitors

  • Tim Cernak
  • , Nathan J. Gesmundo
  • , Kevin Dykstra
  • , Yang Yu
  • , Zhicai Wu
  • , Zhi Cai Shi
  • , Petr Vachal
  • , Donald Sperbeck
  • , Shuwen He
  • , Beth Ann Murphy
  • , Lisa Sonatore
  • , Steven Williams
  • , Maria Madeira
  • , Andreas Verras
  • , Maud Reiter
  • , Claire Heechoon Lee
  • , James Cuff
  • , Edward C. Sherer
  • , Jeffrey Kuethe
  • , Stephen Goble
  • Nicholas Perrotto, Shirly Pinto, Dong Ming Shen, Ravi Nargund, James Balkovec, Robert J. DeVita, Spencer D. Dreher
  • Merck

Research output: Contribution to journal › Article › peer-review

83 Scopus citations

Abstract

Miniaturization and parallel processing play an important role in the evolution of many technologies. We demonstrate the application of miniaturized high-throughput experimentation methods to resolve synthetic chemistry challenges on the frontlines of a lead optimization effort to develop diacylglycerol acyltransferase (DGAT1) inhibitors. Reactions were performed on ∼1 mg scale using glass microvials providing a miniaturized high-throughput experimentation capability that was used to study a challenging SNAr reaction. The availability of robust synthetic chemistry conditions discovered in these miniaturized investigations enabled the development of structure-activity relationships that ultimately led to the discovery of soluble, selective, and potent inhibitors of DGAT1.

Original languageEnglish
Pages (from-to)3594-3605
Number of pages12
JournalJournal of Medicinal Chemistry
Volume60
Issue number9
DOIs
StatePublished - 11 May 2017

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