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Published on: June 7, 2022
Preparation of secolycorines against acetylcholinesterase
Shoei-Sheng Lee1, Uppala Venkatesham, Chitneni Prasad Rao
1School of Pharmacy, College of Medicine, National Taiwan University, 1 Jen-Ai Rd., Sec. 1, Taipei 100, Taiwan, ROC. shoeilee@ha.mc.ntu.edu.tw
Abstract:
5,6-Secolycorines possessing a 5,6-dihydrophenanthridine skeleton were facilely prepared from lycorine through chemical transformations, mainly including N-alkylation, Hofmann degradation type reaction, reductive cleavage of trichloroethylcarbonyl moiety, and hydrogenation. Several secolycorine derivatives showed potent inhibitory activity against acetylcholinesterase with the IC(50) value at micromolar range and are more potent than galanthamine.
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