Structure-based design of non-peptidic pyridone aldehydes as inhibitors of interleukin-1β converting enzyme
摘要:
Pyridone derivatives, especially with 6-aryl substituents, have been shown to be useful P-2-P-3 peptidomimetic scaffolds for the design of potent inhibitors of ICE. (C) 1997 Elsevier Science Ltd.
Structure-based design of non-peptidic pyridone aldehydes as inhibitors of interleukin-1β converting enzyme
摘要:
Pyridone derivatives, especially with 6-aryl substituents, have been shown to be useful P-2-P-3 peptidomimetic scaffolds for the design of potent inhibitors of ICE. (C) 1997 Elsevier Science Ltd.