Literature DB >> 17150789

Convenient synthesis of 3',5'-cyclic diguanylic acid (cdiGMP).

Hongbin Yan1, Eric Humes.   

Abstract

We herein report a convenient synthesis of 3',5'-cyclic diguanylic acid (cdiGMP) through the modified H-phosphonate chemistry. The 1-(4-chlorophenyl)-4-ethoxypiperidin-4-yl (Cpep) group was used as protecting group for the 2'-hydroxy functions of ribonucleosides. Homogeneous cdiGMP was obtained after removal of the protecting groups.

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Year:  2006        PMID: 17150789     DOI: 10.1093/nass/nrl003

Source DB:  PubMed          Journal:  Nucleic Acids Symp Ser (Oxf)        ISSN: 0261-3166


  1 in total

1.  Convenient synthesis of a propargylated cyclic (3'-5') diguanylic acid and its "click" conjugation to a biotinylated azide.

Authors:  Andrzej Grajkowski; Jacek Cieślak; Alexei Gapeev; Christian Schindler; Serge L Beaucage
Journal:  Bioconjug Chem       Date:  2010-10-13       Impact factor: 4.774

  1 in total

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