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A Click-Chemistry Linked 2'3'-cGAMP Analogue.

Clemens Reto DialerSamuele StazzoniDavid Jan DrexlerFelix Moritz MüllerSimon VethAlexander PichlerHidenori OkamuraGregor WitteKarl-Peter HopfnerThomas Carell
Published in: Chemistry (Weinheim an der Bergstrasse, Germany) (2019)
2'3'-cGAMP is an uncanonical cyclic dinucleotide where one A and one G base are connected via a 3'-5' and a unique 2'-5' linkage. The molecule is produced by the cyclase cGAS in response to cytosolic DNA binding. cGAMP activates STING and hence one of the most powerful pathways of innate immunity. cGAMP analogues with uncharged linkages that feature better cellular penetrability are currently highly desired. Here, the synthesis of a cGAMP analogue with one amide and one triazole linkage is reported. The molecule is best prepared via a first CuI -catalyzed click reaction, which establishes the triazole, while the cyclization is achieved by macrolactamization.
Keyphrases
  • dna binding
  • genome wide
  • transcription factor
  • machine learning
  • deep learning
  • gene expression
  • room temperature
  • electron transfer