| Literature DB >> 30536650 |
Clemens Reto Dialer1, Samuele Stazzoni1, David Jan Drexler2, Felix Moritz Müller1, Simon Veth1, Alexander Pichler1, Hidenori Okamura1, Gregor Witte2, Karl-Peter Hopfner2, Thomas Carell1.
Abstract
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.Entities:
Keywords: STING; cGAMP analogue; click chemistry; cyclophane; macrolactamization
Year: 2019 PMID: 30536650 DOI: 10.1002/chem.201805409
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236