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PUBMED FOR HANDHELDS

Journal Abstract Search


164 related items for PubMed ID: 20410615

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  • 3. Synthesis and biological evaluation of novel propargyl amines as potential fluorine-18 labeled radioligands for detection of MAO-B activity.
    Nag S, Kettschau G, Heinrich T, Varrone A, Lehmann L, Gulyas B, Thiele A, Keller É, Halldin C.
    Bioorg Med Chem; 2013 Jan 01; 21(1):186-95. PubMed ID: 23211968
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  • 6. Novel sulfanylphthalimide analogues as highly potent inhibitors of monoamine oxidase B.
    Van der Walt MM, Terre'Blanche G, Petzer A, Petzer JP.
    Bioorg Med Chem Lett; 2012 Nov 01; 22(21):6632-5. PubMed ID: 23010267
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  • 9. Synthesis and in vitro Evaluation of 2-heteroarylidene-1-tetralone Derivatives as Monoamine Oxidase Inhibitors.
    Amakali KT, Legoabe LJ, Petzer A, Petzer JP.
    Drug Res (Stuttg); 2018 Dec 01; 68(12):687-695. PubMed ID: 29758567
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  • 12. Potent and Selective Monoamine Oxidase-B Inhibitory Activity: Fluoro- vs. Trifluoromethyl-4-hydroxylated Chalcone Derivatives.
    Mathew B, Mathew GE, Uçar G, Baysal I, Suresh J, Mathew S, Haridas A, Jayaprakash V.
    Chem Biodivers; 2016 Aug 01; 13(8):1046-52. PubMed ID: 27402375
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  • 14. Potent and highly selective dual-targeting monoamine oxidase-B inhibitors: Fluorinated chalcones of morpholine versus imidazole.
    Mathew B, Baek SC, Thomas Parambi DG, Lee JP, Mathew GE, Jayanthi S, Vinod D, Rapheal C, Devikrishna V, Kondarath SS, Uddin MS, Kim H.
    Arch Pharm (Weinheim); 2019 Apr 01; 352(4):e1800309. PubMed ID: 30663112
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  • 15. Monoamine oxidase inhibition by selected anilide derivatives.
    Legoabe L, Kruger J, Petzer A, Bergh JJ, Petzer JP.
    Eur J Med Chem; 2011 Oct 01; 46(10):5162-74. PubMed ID: 21899930
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  • 16. Combined 3D-QSAR and docking analysis for the design and synthesis of chalcones as potent and selective monoamine oxidase B inhibitors.
    Mellado M, González C, Mella J, Aguilar LF, Viña D, Uriarte E, Cuellar M, Matos MJ.
    Bioorg Chem; 2021 Mar 01; 108():104689. PubMed ID: 33571810
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  • 17. Multipotent MAO and cholinesterase inhibitors for the treatment of Alzheimer's disease: synthesis, pharmacological analysis and molecular modeling of heterocyclic substituted alkyl and cycloalkyl propargyl amine.
    Samadi A, de los Ríos C, Bolea I, Chioua M, Iriepa I, Moraleda I, Bartolini M, Andrisano V, Gálvez E, Valderas C, Unzeta M, Marco-Contelles J.
    Eur J Med Chem; 2012 Jun 01; 52():251-62. PubMed ID: 22503231
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