Feng_2005_Bioorg.Med.Chem.Lett_15_523

Reference

Title : Synthesis and acetylcholinesterase inhibition of derivatives of huperzine B - Feng_2005_Bioorg.Med.Chem.Lett_15_523
Author(s) : Feng S , Xia Y , Han D , Zheng C , He X , Tang X , Bai D
Ref : Bioorganic & Medicinal Chemistry Lett , 15 :523 , 2005
Abstract :

By targeting dual active sites of AChE, a number of new derivatives of HupB have been synthesized and tested as acetylcholinesterase inhibitors. The most potent compound, bis-HupB 5b is 72-fold more potent in AChE inhibition and 79-fold more selective for AChE versus BChE than HupB.

PubMedSearch : Feng_2005_Bioorg.Med.Chem.Lett_15_523
PubMedID: 15664805

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Citations formats

Feng S, Xia Y, Han D, Zheng C, He X, Tang X, Bai D (2005)
Synthesis and acetylcholinesterase inhibition of derivatives of huperzine B
Bioorganic & Medicinal Chemistry Lett 15 :523

Feng S, Xia Y, Han D, Zheng C, He X, Tang X, Bai D (2005)
Bioorganic & Medicinal Chemistry Lett 15 :523