Bis-huperzine B:  Highly Potent and Selective Acetylcholinesterase Inhibitors

Bis-huperzine B:  Highly Potent and Selective Acetylcholinesterase Inhibitors Study on dual-site inhibitors of acetylcholinesterase: Highly potent derivatives of bis- and bifunctional huperzine B Synthesis of more potent analogues of the acetylcholinesterase inhibitor, huperzine B Design, synthesis and evaluation of novel heterodimers of donepezil and huperzine fragments as acetylcholinesterase inhibitors Potent, easily synthesized huperzine A-tacrine hybrid acetylcholinesterase inhibitors Specific Targeting of Acetylcholinesterase and Butyrylcholinesterase Recognition Sites. Rational Design of Novel, Selective, and Highly Potent Cholinesterase Inhibitors Acetylcholinesterase inhibition by tacrine analogues Discovery of Huperzine A−Tacrine Hybrids as Potent Inhibitors of Human Cholinesterases Targeting Their Midgorge Recognition Sites Synthesis of huperzine A, its analogs, and their anticholinesterase activity Rational design and synthesis of highly potent anti-acetylcholinesterase activity huperzine A derivatives