207862-97-3Relevant articles and documents
Synthesis of a benzene-containing C1-phosphonate analogue of UDP-GlcNAc for the inhibition of O-GlcNAc transferase
Im, Jungkyun
, p. 7 - 12 (2016)
I report here the design, synthesis, and biological evaluation of a new C1-phosphonate analogue of UDP-GlcNAc as a potential inhibitor of OGT, an enzyme responsible for O-GlcNAc modification. The analogue was designed to mimic the transition state of the
O-nitrobenzyl photolabile protecting groups with red-shifted absorption: Syntheses and uncaging cross-sections for one- And two-photon excitation
Aujard, Isabelle,Benbrahim, Chouaha,Gouget, Marine,Ruel, Odile,Baudin, Jean-Bernard,Neveu, Pierre,Jullien, Ludovic
, p. 6865 - 6879 (2007/10/03)
We evaluated the o-nitrobenzyl platform for designing photolabile protecting groups with red-shifted absorption that could be photolyzed upon one- and two-photon excitation. Several synthetic pathways to build different conjugated o-nitrobenzyl backbones,