Abstract
Butyrylated NAD+ and its fluorescent analog, 1,N 6-etheno NAD+ are prepared in good yields by employing two-phase system, i.e., water and CH2Cl2 containing dimethyaminopyridine and excess butyric anhydride. The reaction condition for this reaction is so specific that several other acylating conditions attempted were totally failed, and this developed methodology will be conveniently utilized for the further study of cyclic ADP-ribose (cADPR).
Acknowledgments
This work was supported in part by Grant 2000-J-01-B-67 from the Ministry of Science and Technology of Korea, and by Grant R01-2002-000-00114-0(2002) from the Basic Research Program of the Korea Science & Engineering Foundation.