Tan JH

References (10)

Title : Design, synthesis and evaluation of 2-arylethenyl-N-methylquinolinium derivatives as effective multifunctional agents for Alzheimer's disease treatment - Xia_2017_Eur.J.Med.Chem_130_139
Author(s) : Xia CL , Wang N , Guo QL , Liu ZQ , Wu JQ , Huang SL , Ou TM , Tan JH , Wang HG , Li D , Huang ZS
Ref : Eur Journal of Medicinal Chemistry , 130 :139 , 2017
Abstract :
PubMedSearch : Xia_2017_Eur.J.Med.Chem_130_139
PubMedID: 28242549

Title : Design, synthesis, and biological evaluation of 2-arylethenylquinoline derivatives as multifunctional agents for the treatment of Alzheimer's disease - Wang_2014_Eur.J.Med.Chem_89C_349
Author(s) : Wang XQ , Xia CL , Chen SB , Tan JH , Ou TM , Huang SL , Li D , Gu LQ , Huang ZS
Ref : Eur Journal of Medicinal Chemistry , 89C :349 , 2014
Abstract :
PubMedSearch : Wang_2014_Eur.J.Med.Chem_89C_349
PubMedID: 25462251

Title : 2-(2-indolyl-)-4(3H)-quinazolines derivates as new inhibitors of AChE: design, synthesis, biological evaluation and molecular modelling - Li_2013_J.Enzyme.Inhib.Med.Chem_28_583
Author(s) : Li Z , Wang B , Hou JQ , Huang SL , Ou TM , Tan JH , An LK , Li D , Gu LQ , Huang ZS
Ref : J Enzyme Inhib Med Chem , 28 :583 , 2013
Abstract :
PubMedSearch : Li_2013_J.Enzyme.Inhib.Med.Chem_28_583
PubMedID: 22380775

Title : Synthesis and evaluation of 7,8-dehydrorutaecarpine derivatives as potential multifunctional agents for the treatment of Alzheimer's disease - He_2013_Eur.J.Med.Chem_63C_299
Author(s) : He Y , Yao PF , Chen SB , Huang ZH , Huang SL , Tan JH , Li D , Gu LQ , Huang ZS
Ref : Eur Journal of Medicinal Chemistry , 63C :299 , 2013
Abstract :
PubMedSearch : He_2013_Eur.J.Med.Chem_63C_299
PubMedID: 23501115

Title : Design, synthesis and evaluation of isaindigotone derivatives as dual inhibitors for acetylcholinesterase and amyloid beta aggregation - Yan_2012_Bioorg.Med.Chem_20_2527
Author(s) : Yan JW , Li YP , Ye WJ , Chen SB , Hou JQ , Tan JH , Ou TM , Li D , Gu LQ , Huang ZS
Ref : Bioorganic & Medicinal Chemistry , 20 :2527 , 2012
Abstract :
PubMedSearch : Yan_2012_Bioorg.Med.Chem_20_2527
PubMedID: 22444876

Title : Synthesis and biological evaluation of novel N,N'-bis-methylenedioxybenzyl-alkylenediamines as bivalent anti-Alzheimer disease ligands - Luo_2011_J.Enzyme.Inhib.Med.Chem_26_706
Author(s) : Luo W , Li YP , Tan JH , Gu LQ , Huang ZS
Ref : J Enzyme Inhib Med Chem , 26 :706 , 2011
Abstract :
PubMedSearch : Luo_2011_J.Enzyme.Inhib.Med.Chem_26_706
PubMedID: 21250822

Title : Design, synthesis and evaluation of novel tacrine-multialkoxybenzene hybrids as dual inhibitors for cholinesterases and amyloid beta aggregation - Luo_2011_Bioorg.Med.Chem_19_763
Author(s) : Luo W , Li YP , He Y , Huang SL , Tan JH , Ou TM , Li D , Gu LQ , Huang ZS
Ref : Bioorganic & Medicinal Chemistry , 19 :763 , 2011
Abstract :
PubMedSearch : Luo_2011_Bioorg.Med.Chem_19_763
PubMedID: 21211982

Title : Syntheses and characterization of novel oxoisoaporphine derivatives as dual inhibitors for cholinesterases and amyloid beta aggregation - Li_2011_Eur.J.Med.Chem_46_1572
Author(s) : Li YP , Ning FX , Yang MB , Li YC , Nie MH , Ou TM , Tan JH , Huang SL , Li D , Gu LQ , Huang ZS
Ref : Eur Journal of Medicinal Chemistry , 46 :1572 , 2011
Abstract :
PubMedSearch : Li_2011_Eur.J.Med.Chem_46_1572
PubMedID: 21367493

Title : Synthesis and evaluation of novel rutaecarpine derivatives and related alkaloids derivatives as selective acetylcholinesterase inhibitors - Wang_2010_Eur.J.Med.Chem_45_1415
Author(s) : Wang B , Mai YC , Li Y , Hou JQ , Huang SL , Ou TM , Tan JH , An LK , Li D , Gu LQ , Huang ZS
Ref : Eur Journal of Medicinal Chemistry , 45 :1415 , 2010
Abstract :
PubMedSearch : Wang_2010_Eur.J.Med.Chem_45_1415
PubMedID: 20079560

Title : Design, synthesis and evaluation of isaindigotone derivatives as acetylcholinesterase and butyrylcholinesterase inhibitors - Pan_2008_Bioorg.Med.Chem.Lett_18_3790
Author(s) : Pan L , Tan JH , Hou JQ , Huang SL , Gu LQ , Huang ZS
Ref : Bioorganic & Medicinal Chemistry Lett , 18 :3790 , 2008
Abstract :
PubMedSearch : Pan_2008_Bioorg.Med.Chem.Lett_18_3790
PubMedID: 18524585