Report for Huang ZS

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References (17)

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 : Xia_2017_Eur.J.Med.Chem_130_139
ESTHER : Xia_2017_Eur.J.Med.Chem_130_139
PubMedSearch : Xia_2017_Eur.J.Med.Chem_130_139
PubMedID: 28242549

Title : Synthesis and characterization of 1H-phenanthro[9,10-d]imidazole derivatives as multifunctional agents for treatment of Alzheimer's disease - Liu_2014_Biochim.Biophys.Acta_1840_2886
Author(s) : Liu J , Qiu J , Wang M , Wang L , Su L , Gao J , Gu Q , Xu J , Huang SL , Gu LQ , Huang ZS , Li D
Ref : Biochimica & Biophysica Acta , 1840 :2886 , 2014
Abstract : Liu_2014_Biochim.Biophys.Acta_1840_2886
ESTHER : Liu_2014_Biochim.Biophys.Acta_1840_2886
PubMedSearch : Liu_2014_Biochim.Biophys.Acta_1840_2886
PubMedID: 24821011

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 : Wang_2014_Eur.J.Med.Chem_89C_349
ESTHER : Wang_2014_Eur.J.Med.Chem_89C_349
PubMedSearch : Wang_2014_Eur.J.Med.Chem_89C_349
PubMedID: 25462251

Title : 3D-QSAR studies of azaoxoisoaporphine, oxoaporphine, and oxoisoaporphine derivatives as anti-AChE and anti-AD agents by the CoMFA method - Li_2013_J.Mol.Graph.Model_41C_61
Author(s) : Li YP , Weng X , Ning FX , Ou JB , Hou JQ , Luo HB , Li D , Huang ZS , Huang SL , Gu LQ
Ref : J Mol Graph Model , 41C :61 , 2013
Abstract : Li_2013_J.Mol.Graph.Model_41C_61
ESTHER : Li_2013_J.Mol.Graph.Model_41C_61
PubMedSearch : Li_2013_J.Mol.Graph.Model_41C_61
PubMedID: 23500628

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 : He_2013_Eur.J.Med.Chem_63C_299
ESTHER : He_2013_Eur.J.Med.Chem_63C_299
PubMedSearch : He_2013_Eur.J.Med.Chem_63C_299
PubMedID: 23501115

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 : Li_2013_J.Enzyme.Inhib.Med.Chem_28_583
ESTHER : Li_2013_J.Enzyme.Inhib.Med.Chem_28_583
PubMedSearch : Li_2013_J.Enzyme.Inhib.Med.Chem_28_583
PubMedID: 22380775

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 : Yan_2012_Bioorg.Med.Chem_20_2527
ESTHER : Yan_2012_Bioorg.Med.Chem_20_2527
PubMedSearch : Yan_2012_Bioorg.Med.Chem_20_2527
PubMedID: 22444876

Title : Synthesis and acetylcholinesterase and butyrylcholinesterase inhibitory activities of 7-alkoxyl substituted indolizinoquinoline-5,12-dione derivatives - Wu_2012_Arch.Pharm.(Weinheim)_345_175
Author(s) : Wu ZP , Wu XW , Shen T , Li YP , Cheng X , Gu LQ , Huang ZS , An LK
Ref : Arch Pharm (Weinheim) , 345 :175 , 2012
Abstract : Wu_2012_Arch.Pharm.(Weinheim)_345_175
ESTHER : Wu_2012_Arch.Pharm.(Weinheim)_345_175
PubMedSearch : Wu_2012_Arch.Pharm.(Weinheim)_345_175
PubMedID: 21989769

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 : Li_2011_Eur.J.Med.Chem_46_1572
ESTHER : Li_2011_Eur.J.Med.Chem_46_1572
PubMedSearch : Li_2011_Eur.J.Med.Chem_46_1572
PubMedID: 21367493

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 : Luo_2011_J.Enzyme.Inhib.Med.Chem_26_706
ESTHER : Luo_2011_J.Enzyme.Inhib.Med.Chem_26_706
PubMedSearch : Luo_2011_J.Enzyme.Inhib.Med.Chem_26_706
PubMedID: 21250822

Title : Hybrids of oxoisoaporphine-tacrine congeners: novel acetylcholinesterase and acetylcholinesterase-induced beta-amyloid aggregation inhibitors - Tang_2011_Eur.J.Med.Chem_46_4970
Author(s) : Tang H , Zhao LZ , Zhao HT , Huang SL , Zhong SM , Qin JK , Chen ZF , Huang ZS , Liang H
Ref : Eur Journal of Medicinal Chemistry , 46 :4970 , 2011
Abstract : Tang_2011_Eur.J.Med.Chem_46_4970
ESTHER : Tang_2011_Eur.J.Med.Chem_46_4970
PubMedSearch : Tang_2011_Eur.J.Med.Chem_46_4970
PubMedID: 21871694

Title : Synthesis and evaluation of heterobivalent tacrine derivatives as potential multi-functional anti-Alzheimer agents - Luo_2011_Eur.J.Med.Chem_46_2609
Author(s) : Luo W , Li YP , He Y , Huang SL , Li D , Gu LQ , Huang ZS
Ref : Eur Journal of Medicinal Chemistry , 46 :2609 , 2011
Abstract : Luo_2011_Eur.J.Med.Chem_46_2609
ESTHER : Luo_2011_Eur.J.Med.Chem_46_2609
PubMedSearch : Luo_2011_Eur.J.Med.Chem_46_2609
PubMedID: 21497959

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 : Luo_2011_Bioorg.Med.Chem_19_763
ESTHER : Luo_2011_Bioorg.Med.Chem_19_763
PubMedSearch : Luo_2011_Bioorg.Med.Chem_19_763
PubMedID: 21211982

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 : Wang_2010_Eur.J.Med.Chem_45_1415
ESTHER : Wang_2010_Eur.J.Med.Chem_45_1415
PubMedSearch : Wang_2010_Eur.J.Med.Chem_45_1415
PubMedID: 20079560

Title : Synthesis, biological evaluation and molecular modeling of oxoisoaporphine and oxoaporphine derivatives as new dual inhibitors of acetylcholinesterase\/butyrylcholinesterase - Tang_2009_Eur.J.Med.Chem_44_2523
Author(s) : Tang H , Wei YB , Zhang C , Ning FX , Qiao W , Huang SL , Ma L , Huang ZS , Gu LQ
Ref : Eur Journal of Medicinal Chemistry , 44 :2523 , 2009
Abstract : Tang_2009_Eur.J.Med.Chem_44_2523
ESTHER : Tang_2009_Eur.J.Med.Chem_44_2523
PubMedSearch : Tang_2009_Eur.J.Med.Chem_44_2523
PubMedID: 19243862

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 : Pan_2008_Bioorg.Med.Chem.Lett_18_3790
ESTHER : Pan_2008_Bioorg.Med.Chem.Lett_18_3790
PubMedSearch : Pan_2008_Bioorg.Med.Chem.Lett_18_3790
PubMedID: 18524585

Title : Derivatives of oxoisoaporphine alkaloids: a novel class of selective acetylcholinesterase inhibitors - Tang_2007_Bioorg.Med.Chem.Lett_17_3765
Author(s) : Tang H , Ning FX , Wei YB , Huang SL , Huang ZS , Chan AS , Gu LQ
Ref : Bioorganic & Medicinal Chemistry Lett , 17 :3765 , 2007
Abstract : Tang_2007_Bioorg.Med.Chem.Lett_17_3765
ESTHER : Tang_2007_Bioorg.Med.Chem.Lett_17_3765
PubMedSearch : Tang_2007_Bioorg.Med.Chem.Lett_17_3765
PubMedID: 17451950