3,6-Disubstituted pyridazine analogs (2a and 2b) were synthesized from commercially available 3,6- dichloropyridazine in two steps. The synthesized compounds were evaluated for their GPR119 agonistic activity. Both compounds exhibited much stronger EC50 values than that of oleylethanolamide (OEA) and were proved to be partial agonists. These results indicate that the pyridazine ring can be used as a potential heterocycle scaffold for GPR119 agonists.
서 론(Introduction)
방 법(Methods)
결과 및 고찰(Results and Discussion)
결 론(Conclusion)
감사의 말씀(Acknowledgment)
Conflict of Interest
References