| Literature DB >> 30938482 |
Cedric J Stress1, Basilius Sauter1, Lukas A Schneider1, Timothy Sharpe2, Dennis Gillingham1.
Abstract
Here we show a seven-step chemical synthesis of a DNA-encoded macrocycle library (DEML) on DNA. Inspired by polyketide and mixed peptide-polyketide natural products, the library was designed to incorporate rich backbone diversity. Achieving this diversity, however, comes at the cost of the custom synthesis of bifunctional building block libraries. This study outlines the importance of careful retrosynthetic design in DNA-encoded libraries, while revealing areas where new DNA synthetic methods are needed.Entities:
Keywords: DNA chemistry; DNA-encoded libraries; Lipinski rules; chemical libraries; macrocycles
Year: 2019 PMID: 30938482 DOI: 10.1002/anie.201902513
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336