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Journal Abstract Search

726 related items for PubMed ID: 29655693

  • 1. Molecular modeling and in vitro approaches towards cholinesterase inhibitory effect of some natural xanthohumol, naringenin, and acyl phloroglucinol derivatives.
    Orhan IE, Jedrejek D, Senol FS, Salmas RE, Durdagi S, Kowalska I, Pecio L, Oleszek W.
    Phytomedicine; 2018 Mar 15; 42():25-33. PubMed ID: 29655693
    [Abstract] [Full Text] [Related]

  • 2. Combined molecular modeling and cholinesterase inhibition studies on some natural and semisynthetic O-alkylcoumarin derivatives.
    Orhan IE, Senol Deniz FS, Salmas RE, Durdagi S, Epifano F, Genovese S, Fiorito S.
    Bioorg Chem; 2019 Mar 15; 84():355-362. PubMed ID: 30530106
    [Abstract] [Full Text] [Related]

  • 3. Design, synthesis, and evaluation of novel cinnamic acid-tryptamine hybrid for inhibition of acetylcholinesterase and butyrylcholinesterase.
    Ghafary S, Ghobadian R, Mahdavi M, Nadri H, Moradi A, Akbarzadeh T, Najafi Z, Sharifzadeh M, Edraki N, Moghadam FH, Amini M.
    Daru; 2020 Dec 15; 28(2):463-477. PubMed ID: 32372339
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  • 4. In Silico Docking and In Vitro Approaches towards BACE1 and Cholinesterases Inhibitory Effect of Citrus Flavanones.
    Lee S, Youn K, Lim G, Lee J, Jun M.
    Molecules; 2018 Jun 22; 23(7):. PubMed ID: 29932100
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  • 5. Identification of New Chromenone Derivatives as Cholinesterase Inhibitors and Molecular Docking Studies.
    Iqbal J, Abbasi MSA, Zaib S, Afridi S, Furtmann N, Bajorath J, Langer P.
    Med Chem; 2018 Jun 22; 14(8):809-817. PubMed ID: 29473519
    [Abstract] [Full Text] [Related]

  • 6. Profiling Auspicious Butyrylcholinesterase Inhibitory Activity of Two Herbal Molecules: Hyperforin and Hyuganin C.
    Orhan IE, Senol Deniz FS, Traedal-Henden S, Cerón-Carrasco JP, den Haan H, Peña-García J, Pérez-Sánchez H, Emerce E, Skalicka-Wozniak K.
    Chem Biodivers; 2019 May 22; 16(5):e1900017. PubMed ID: 30891904
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  • 7. In silico, theoretical biointerface analysis and in vitro kinetic analysis of amine compounds interaction with acetylcholinesterase and butyrylcholinesterase.
    Kandasamy S, Loganathan C, Sakayanathan P, Karthikeyan S, Stephen AD, Marimuthu DK, Ravichandran S, Sivalingam V, Thayumanavan P.
    Int J Biol Macromol; 2021 Aug 31; 185():750-760. PubMed ID: 34216669
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  • 8. Molecular-docking-guided design and synthesis of new IAA-tacrine hybrids as multifunctional AChE/BChE inhibitors.
    Cheng ZQ, Zhu KK, Zhang J, Song JL, Muehlmann LA, Jiang CS, Liu CL, Zhang H.
    Bioorg Chem; 2019 Mar 31; 83():277-288. PubMed ID: 30391700
    [Abstract] [Full Text] [Related]

  • 9. Synthesis, Characterization and Cholinesterase Inhibition Studies of New Arylidene Aminothiazolylethanone Derivatives.
    Channar PA, Shah MS, Saeed A, Khan SU, Larik FA, Shabir G, Iqbal J.
    Med Chem; 2017 Mar 31; 13(7):648-653. PubMed ID: 28266279
    [Abstract] [Full Text] [Related]

  • 10. Synthesis and cholinesterase inhibitory activity study of new piperidone grafted spiropyrrolidines.
    Basiri A, Abd Razik BM, Ezzat MO, Kia Y, Kumar RS, Almansour AI, Arumugam N, Murugaiyah V.
    Bioorg Chem; 2017 Dec 31; 75():210-216. PubMed ID: 28987876
    [Abstract] [Full Text] [Related]

  • 11. Bis-Amiridines as Acetylcholinesterase and Butyrylcholinesterase Inhibitors: N-Functionalization Determines the Multitarget Anti-Alzheimer's Activity Profile.
    Makhaeva GF, Kovaleva NV, Boltneva NP, Rudakova EV, Lushchekina SV, Astakhova TY, Serkov IV, Proshin AN, Radchenko EV, Palyulin VA, Korabecny J, Soukup O, Bachurin SO, Richardson RJ.
    Molecules; 2022 Feb 04; 27(3):. PubMed ID: 35164325
    [Abstract] [Full Text] [Related]

  • 12. Design, Synthesis and Investigation of New Diphenyl Substituted Pyridazinone Derivatives as Both Cholinesterase and Aβ-Aggregation Inhibitors.
    Kilic B, Erdogan M, Gulcan HO, Aksakal F, Oruklu N, Bagriacik EU, Dogruer DS.
    Med Chem; 2019 Feb 04; 15(1):59-76. PubMed ID: 29792155
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  • 13. Pyridine sulfonamide as a small key organic molecule for the potential treatment of type-II diabetes mellitus and Alzheimer's disease: In vitro studies against yeast α-glucosidase, acetylcholinesterase and butyrylcholinesterase.
    Riaz S, Khan IU, Bajda M, Ashraf M, Qurat-Ul-Ain, Shaukat A, Rehman TU, Mutahir S, Hussain S, Mustafa G, Yar M.
    Bioorg Chem; 2015 Dec 04; 63():64-71. PubMed ID: 26451651
    [Abstract] [Full Text] [Related]

  • 14. Syntheses, cholinesterases inhibition, and molecular docking studies of pyrido[2,3-b]pyrazine derivatives.
    Hameed A, Zehra ST, Shah SJ, Khan KM, Alharthy RD, Furtmann N, Bajorath J, Tahir MN, Iqbal J.
    Chem Biol Drug Des; 2015 Nov 04; 86(5):1115-20. PubMed ID: 25951978
    [Abstract] [Full Text] [Related]

  • 15. Novel biphenyl bis-sulfonamides as acetyl and butyrylcholinesterase inhibitors: Synthesis, biological evaluation and molecular modeling studies.
    Mutahir S, Jończyk J, Bajda M, Khan IU, Khan MA, Ullah N, Ashraf M, Qurat-ul-Ain, Riaz S, Hussain S, Yar M.
    Bioorg Chem; 2016 Feb 04; 64():13-20. PubMed ID: 26595185
    [Abstract] [Full Text] [Related]

  • 16. Design and synthesis of some new carboxamide and propanamide derivatives bearing phenylpyridazine as a core ring and the investigation of their inhibitory potential on in-vitro acetylcholinesterase and butyrylcholinesterase.
    Kilic B, Gulcan HO, Aksakal F, Ercetin T, Oruklu N, Umit Bagriacik E, Dogruer DS.
    Bioorg Chem; 2018 Sep 04; 79():235-249. PubMed ID: 29775949
    [Abstract] [Full Text] [Related]

  • 17. Design, synthesis and evaluation of novel 4-dimethylamine flavonoid derivatives as potential multi-functional anti-Alzheimer agents.
    Luo W, Su YB, Hong C, Tian RG, Su LP, Wang YQ, Li Y, Yue JJ, Wang CJ.
    Bioorg Med Chem; 2013 Dec 01; 21(23):7275-82. PubMed ID: 24148835
    [Abstract] [Full Text] [Related]

  • 18. Pteryxin - A promising butyrylcholinesterase-inhibiting coumarin derivative from Mutellina purpurea.
    Orhan IE, Senol FS, Shekfeh S, Skalicka-Wozniak K, Banoglu E.
    Food Chem Toxicol; 2017 Nov 01; 109(Pt 2):970-974. PubMed ID: 28286309
    [Abstract] [Full Text] [Related]

  • 19. Synthesis, structure-activity relationship and molecular docking of 3-oxoaurones and 3-thioaurones as acetylcholinesterase and butyrylcholinesterase inhibitors.
    Mughal EU, Sadiq A, Murtaza S, Rafique H, Zafar MN, Riaz T, Khan BA, Hameed A, Khan KM.
    Bioorg Med Chem; 2017 Jan 01; 25(1):100-106. PubMed ID: 27780618
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  • 20. Cholinesterase Inhibitory and In Silico Toxicity Assessment of Thirty-Four Isoquinoline Alkaloids - Berberine as the Lead Compound.
    Senol Deniz FS, Ekhteiari Salmas R, Emerce E, Sener B, Orhan IE.
    CNS Neurol Disord Drug Targets; 2024 Jan 01; 23(6):773-783. PubMed ID: 37073143
    [Abstract] [Full Text] [Related]

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