2-Fluorophenyl isocyanate reacted with adamantan-1(2)-amines and their homologs in DMF to give 31–92% of the corresponding N,N′-disubstituted ureas that are target-oriented human soluble epoxide hydrolase (sEH) inhibitors. Introduction of a fluorine atom increases the sEH inhibitory activity by a factor of 4.5.
2-氟苯基异氰酸酯与adamantan-1(2)-胺及其在
DMF中的同系物反应,得到31-92%的相应N,N'-二取代
尿素,它们是靶标定向的人类可溶性环氧
水解酶(sEH)
抑制剂。引入
氟原子可使sEH抑制活性提高4.5倍。