Potent, easily synthesized huperzine A-tacrine hybrid acetylcholinesterase inhibitors

Bioorganic and Medicinal Chemistry Letters

Volumn 9, Issue 16, 1999, Pages 2335-2338

  Carlier, Paul R ^a   Du, Da Ming ^a   Han, Yifan ^a   Liu, Jing ^a   Pang, Yuan Ping ^b  

^a HONG KONG UNIVERSITY OF SCIENCE AND TECHNOLOGY   (Hong Kong)

^b MAYO CLINIC CANCER CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CHOLINESTERASE INHIBITOR; HUPERZINE A; HUPERZINE A TACRINE; QUINOLINE DERIVATIVE; TACRINE; UNCLASSIFIED DRUG;

ALZHEIMER DISEASE; ANIMAL TISSUE; ARTICLE; CONTROLLED STUDY; DRUG POTENCY; DRUG SELECTIVITY; DRUG STRUCTURE; DRUG SYNTHESIS; ENZYME INHIBITION; HYBRIDIZATION; NONHUMAN; RAT;

ACETYLCHOLINESTERASE; CHOLINESTERASE INHIBITORS; SESQUITERPENES; TACRINE;

EID: 0033575679     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0960-894X(99)00396-0     Document Type: Article

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