Hou JQ

References (5)

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 : 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 : 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 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 : 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