Sun_2013_Bioorg.Med.Chem_21_7406

Reference

Title : Inhibition of cholinesterase and monoamine oxidase-B activity by Tacrine-Homoisoflavonoid hybrids - Sun_2013_Bioorg.Med.Chem_21_7406
Author(s) : Sun Y , Chen J , Chen X , Huang L , Li X
Ref : Bioorganic & Medicinal Chemistry , 21 :7406 , 2013
Abstract : A series of Tacrine-Homoisoflavonoid hybrids were designed, synthesised and evaluated as inhibitors of cholinesterases (ChEs) and human monoamine oxidases (MAOs). Most of the compounds were found to be potent against both ChEs and MAO-B. Among these hybrids, compound 8b, with a 6 carbon linker between tacrine and (E)-7-hydroxy-3-(4-methoxybenzylidene)chroman-4-one, proved to be the most potent against AChE and MAO-B with IC50 values of 67.9nM and 0.401muM, respectively. This compound was observed to cross the blood-brain barrier (BBB) in a parallel artificial membrane permeation assay for the BBB (PAMPA-BBB). The results indicated that compound 8b is an excellent multifunctional promising compound for development of novel drugs for Alzheimer's disease (AD).
ESTHER : Sun_2013_Bioorg.Med.Chem_21_7406
PubMedSearch : Sun_2013_Bioorg.Med.Chem_21_7406
PubMedID: 24128814

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Citations formats

Sun Y, Chen J, Chen X, Huang L, Li X (2013)
Inhibition of cholinesterase and monoamine oxidase-B activity by Tacrine-Homoisoflavonoid hybrids
Bioorganic & Medicinal Chemistry 21 :7406

Sun Y, Chen J, Chen X, Huang L, Li X (2013)
Bioorganic & Medicinal Chemistry 21 :7406