2024-03-29T01:38:45Zhttps://eprints.lib.hokudai.ac.jp/dspace-oai/requestoai:eprints.lib.hokudai.ac.jp:2115/648902022-11-17T02:08:08Zhdl_2115_20046hdl_2115_138Selective Hydrogenation and Transfer Hydrogenation for Post-Functional Synthesis of Trifluoromethylphenyl Diazirine Derivatives for Photoaffinity Labeling1000090292094Hashimoto, MakotoMurai, YutaHolman, Geoffery D.Hatanaka, Yasumaruopen accessCreative Commons Attribution 3.0 Unportedhydrogenationphotoaffinity labelingElucidation of protein functions on the basis of structure–activity relationships can reveal the mechanisms of homeostasis functions in life and is one of the greatest interests of scientists. In the human body, many proteins are activated and/or inactivated by ligands to maintain homeostasis. Understanding the mechanism of molecular interactions between small bioactive ligands and proteins is an important step in rational drug design and discovery. ! Photoaffinity labeling, which is one of the most familiar approaches for chemical biology analysis, was initiated using diazocarbonyl derivatives in 1962 (Singh et al., 1962). Many researchers have subsequently tried to establish alternative approaches for the direct identification of target proteins for the bioactive small ligands. These approaches are based on the affinity between the ligand and the target protein (Figure 1). Several reviews are published for the recent applications of photoaffinity labeling (Tomohiro et al., 2005; Hashimoto & Hatanaka, 2008). To archive photoaffinity labeling, researchers have to prepare photoaffinity labeling ligands. The native ligands must be modified by photoreactive compounds (photophores) by organic synthesisIn Tech2012-10-10engbook partVoRhttp://hdl.handle.net/2115/64890Hydrogenation, edited by Iyad Karame. Chapter 5https://doi.org/10.5772/48730121136https://eprints.lib.hokudai.ac.jp/dspace/bitstream/2115/64890/1/14%20%20Hydrogenation%20%28book%29%20%20121-136%202012%20.pdfapplication/pdf382.55 KB2012-10-10