文摘
Design, synthesis and biological evaluation of piperlongumine (PL) derived cyclic sulfonamides has been described. In vitro exploration for therapeutic potential against HeLa cervical cancer cells. Ring closing metathesis approach using Grubbs II catalyst. Synthesized small library of new scaffold (piperlongumine derived cyclic sulphonamides). Of these NPL-07, NPL-10 and NPL-14 significantly reduced the cell growth and may serve as lead for development for treatment of cancer area.