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Journal Abstract Search

259 related items for PubMed ID: 16137794

  • 1. Synthesis and biological evaluation as AChE inhibitors of new indanones and thiaindanones related to donepezil.
    Omran Z, Cailly T, Lescot E, Santos JS, Agondanou JH, Lisowski V, Fabis F, Godard AM, Stiebing S, Le Flem G, Boulouard M, Dauphin F, Dallemagne P, Rault S.
    Eur J Med Chem; 2005 Dec; 40(12):1222-45. PubMed ID: 16137794
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  • 2. Synthesis and biological activity of new donepezil-hydrazinonicotinamide hybrids.
    Zurek E, Szymański P, Mikiciuk-Olasik E.
    Drug Res (Stuttg); 2013 Mar; 63(3):137-44. PubMed ID: 23447117
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  • 3. Design, synthesis and evaluation of novel heterodimers of donepezil and huperzine fragments as acetylcholinesterase inhibitors.
    Hu Y, Zhang J, Chandrashankra O, Ip FC, Ip NY.
    Bioorg Med Chem; 2013 Feb 01; 21(3):676-83. PubMed ID: 23273608
    [Abstract] [Full Text] [Related]

  • 4. Synthesis, biological evaluation, and molecular modeling of donepezil and N-[(5-(benzyloxy)-1-methyl-1H-indol-2-yl)methyl]-N-methylprop-2-yn-1-amine hybrids as new multipotent cholinesterase/monoamine oxidase inhibitors for the treatment of Alzheimer's disease.
    Bolea I, Juárez-Jiménez J, de Los Ríos C, Chioua M, Pouplana R, Luque FJ, Unzeta M, Marco-Contelles J, Samadi A.
    J Med Chem; 2011 Dec 22; 54(24):8251-70. PubMed ID: 22023459
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  • 5. Synthesis, in vitro assay, and molecular modeling of new piperidine derivatives having dual inhibitory potency against acetylcholinesterase and Abeta1-42 aggregation for Alzheimer's disease therapeutics.
    Kwon YE, Park JY, No KT, Shin JH, Lee SK, Eun JS, Yang JH, Shin TY, Kim DK, Chae BS, Leem JY, Kim KH.
    Bioorg Med Chem; 2007 Oct 15; 15(20):6596-607. PubMed ID: 17681794
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  • 6. Synthesis and biological evaluation of new donepezil-like Thiaindanones as AChE inhibitors.
    Omran Z, Stiebing S, Godard AM, Sopkova-De Oliveira-Santos J, Dallemagne P.
    J Enzyme Inhib Med Chem; 2008 Oct 15; 23(5):696-703. PubMed ID: 18821258
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  • 7. [Synthesis and AchE inhibitory activity of 2-phenoxy-indan-1-one derivatives].
    Sheng R, Lin X, Li JY, Hu YZ.
    Yao Xue Xue Bao; 2006 Feb 15; 41(2):115-20. PubMed ID: 16671539
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  • 11. 2-Phenoxy-indan-1-one derivatives as acetylcholinesterase inhibitors: a study on the importance of modifications at the side chain on the activity.
    Shen Y, Sheng R, Zhang J, He Q, Yang B, Hu Y.
    Bioorg Med Chem; 2008 Aug 15; 16(16):7646-53. PubMed ID: 18662884
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  • 16. Synthesis and pharmacological evaluation of donepezil-based agents as new cholinesterase/monoamine oxidase inhibitors for the potential application against Alzheimer's disease.
    Li F, Wang ZM, Wu JJ, Wang J, Xie SS, Lan JS, Xu W, Kong LY, Wang XB.
    J Enzyme Inhib Med Chem; 2016 Aug 15; 31(sup3):41-53. PubMed ID: 27384289
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  • 17. Design, synthesis, pharmacological evaluation, QSAR analysis, molecular modeling and ADMET of novel donepezil-indolyl hybrids as multipotent cholinesterase/monoamine oxidase inhibitors for the potential treatment of Alzheimer's disease.
    Bautista-Aguilera OM, Esteban G, Bolea I, Nikolic K, Agbaba D, Moraleda I, Iriepa I, Samadi A, Soriano E, Unzeta M, Marco-Contelles J.
    Eur J Med Chem; 2014 Mar 21; 75():82-95. PubMed ID: 24530494
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  • 18. Synthesis of new donepezil analogues and investigation of their effects on cholinesterase enzymes.
    Sağlık BN, Ilgın S, Özkay Y.
    Eur J Med Chem; 2016 Nov 29; 124():1026-1040. PubMed ID: 27783974
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  • 19. 7-MEOTA-donepezil like compounds as cholinesterase inhibitors: Synthesis, pharmacological evaluation, molecular modeling and QSAR studies.
    Korabecny J, Dolezal R, Cabelova P, Horova A, Hruba E, Ricny J, Sedlacek L, Nepovimova E, Spilovska K, Andrs M, Musilek K, Opletalova V, Sepsova V, Ripova D, Kuca K.
    Eur J Med Chem; 2014 Jul 23; 82():426-38. PubMed ID: 24929293
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  • 20. Pyridonepezils, new dual AChE inhibitors as potential drugs for the treatment of Alzheimer's disease: synthesis, biological assessment, and molecular modeling.
    Samadi A, Estrada M, Pérez C, Rodríguez-Franco MI, Iriepa I, Moraleda I, Chioua M, Marco-Contelles J.
    Eur J Med Chem; 2012 Nov 23; 57():296-301. PubMed ID: 23078965
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