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Journal Abstract Search

790 related items for PubMed ID: 26438408

  • 41. Quantitative structure-activity relationship (QSAR) of tacrine derivatives against acetylcholinesterase (AChE) activity using variable selections.
    Jung M, Tak J, Lee Y, Jung Y.
    Bioorg Med Chem Lett; 2007 Feb 15; 17(4):1082-90. PubMed ID: 17158047
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  • 42. 2D-SAR and 3D-QSAR analyses for acetylcholinesterase inhibitors.
    Niu B, Zhao M, Su Q, Zhang M, Lv W, Chen Q, Chen F, Chu D, Du D, Zhang Y.
    Mol Divers; 2017 May 15; 21(2):413-426. PubMed ID: 28275924
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  • 43. Exploring molecular structural requirement for AChE inhibition through multi-chemometric and dynamics simulation analyses.
    Hossain T, Saha A, Mukherjee A.
    J Biomol Struct Dyn; 2018 Apr 15; 36(5):1274-1285. PubMed ID: 28417668
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  • 44. Synthesis and biological evaluation of novel tacrine derivatives and tacrine-coumarin hybrids as cholinesterase inhibitors.
    Hamulakova S, Janovec L, Hrabinova M, Spilovska K, Korabecny J, Kristian P, Kuca K, Imrich J.
    J Med Chem; 2014 Aug 28; 57(16):7073-84. PubMed ID: 25089370
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  • 45. 3D structure of Torpedo californica acetylcholinesterase complexed with huprine X at 2.1 A resolution: kinetic and molecular dynamic correlates.
    Dvir H, Wong DM, Harel M, Barril X, Orozco M, Luque FJ, Muñoz-Torrero D, Camps P, Rosenberry TL, Silman I, Sussman JL.
    Biochemistry; 2002 Mar 05; 41(9):2970-81. PubMed ID: 11863435
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  • 48. Identification of Human Acetylcholinesterase Inhibitors from the Constituents of EGb761 by Modeling Docking and Molecular Dynamics Simulations.
    Zhang L, Li D, Cao F, Xiao W, Zhao L, Ding G, Wang ZZ.
    Comb Chem High Throughput Screen; 2018 Mar 05; 21(1):41-49. PubMed ID: 29173156
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  • 50. Synthesis, molecular docking and molecular dynamics studies of novel tacrine-carbamate derivatives as potent cholinesterase inhibitors.
    Ozten O, Zengin Kurt B, Sonmez F, Dogan B, Durdagi S.
    Bioorg Chem; 2021 Oct 05; 115():105225. PubMed ID: 34364052
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  • 52. 3D-QSAR analysis of a new type of acetylcholinesterase inhibitors.
    Liu A, Guang H, Zhu L, Du G, Lee SM, Wang Y.
    Sci China C Life Sci; 2007 Dec 05; 50(6):726-30. PubMed ID: 17914643
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  • 53. Cooperative hydrogen bonds and mobility of the non-aromatic ring as selectivity determinants for human acetylcholinesterase to similar anti-Alzheimer's galantaminics: a computational study.
    Rocha REO, Lima LHF.
    J Biomol Struct Dyn; 2019 Apr 05; 37(7):1843-1856. PubMed ID: 29697300
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  • 56. A cascade synthesis, in vitro cholinesterases inhibitory activity and docking studies of novel Tacrine-pyranopyrazole derivatives.
    Derabli C, Boualia I, Abdelwahab AB, Boulcina R, Bensouici C, Kirsch G, Debache A.
    Bioorg Med Chem Lett; 2018 Aug 01; 28(14):2481-2484. PubMed ID: 29887354
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  • 60. Development of 2-Methoxyhuprine as Novel Lead for Alzheimer's Disease Therapy.
    Mezeiova E, Korabecny J, Sepsova V, Hrabinova M, Jost P, Muckova L, Kucera T, Dolezal R, Misik J, Spilovska K, Pham NL, Pokrievkova L, Roh J, Jun D, Soukup O, Kaping D, Kuca K.
    Molecules; 2017 Jul 28; 22(8):. PubMed ID: 28788095
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