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Journal Abstract Search

379 related items for PubMed ID: 10446376

  • 1. Amino acid residues involved in the interaction of acetylcholinesterase and butyrylcholinesterase with the carbamates Ro 02-0683 and bambuterol, and with terbutaline.
    Kovarik Z, Radić Z, Grgas B, Skrinjarić-Spoljar M, Reiner E, Simeon-Rudolf V.
    Biochim Biophys Acta; 1999 Aug 17; 1433(1-2):261-71. PubMed ID: 10446376
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  • 8. Acetylcholinesterase active centre and gorge conformations analysed by combinatorial mutations and enantiomeric phosphonates.
    Kovarik Z, Radić Z, Berman HA, Simeon-Rudolf V, Reiner E, Taylor P.
    Biochem J; 2003 Jul 01; 373(Pt 1):33-40. PubMed ID: 12665427
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  • 9. Bambuterol, a carbamate ester prodrug of terbutaline, as inhibitor of cholinesterases in human blood.
    Tunek A, Svensson LA.
    Drug Metab Dispos; 1988 Jul 01; 16(5):759-64. PubMed ID: 2906603
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  • 10. Reversible inhibition of acetylcholinesterase and butyrylcholinesterase by 4,4'-bipyridine and by a coumarin derivative.
    Simeon-Rudolf V, Kovarik Z, Radić Z, Reiner E.
    Chem Biol Interact; 1999 May 14; 119-120():119-28. PubMed ID: 10421445
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  • 11. Metaproterenol, isoproterenol, and their bisdimethylcarbamate derivatives as human cholinesterase inhibitors.
    Bosak A, Gazić Smilović I, Sinko G, Vinković V, Kovarik Z.
    J Med Chem; 2012 Aug 09; 55(15):6716-23. PubMed ID: 22817559
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  • 12. 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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  • 13. Design, synthesis and biological evaluation of novel carbamates as potential inhibitors of acetylcholinesterase and butyrylcholinesterase.
    Wu J, Pistolozzi M, Liu S, Tan W.
    Bioorg Med Chem; 2020 Mar 01; 28(5):115324. PubMed ID: 32008882
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  • 14. Stereoselective inhibition of human butyrylcholinesterase by the enantiomers of bambuterol and their intermediates.
    Pistolozzi M, Du H, Wei H, Tan W.
    Drug Metab Dispos; 2015 Mar 01; 43(3):344-52. PubMed ID: 25504505
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  • 15. Molecular dissection of cholinesterase domains responsible for carbamate toxicity.
    Loewenstein Y, Denarie M, Zakut H, Soreq H.
    Chem Biol Interact; 1993 Jun 01; 87(1-3):209-16. PubMed ID: 8343977
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  • 16. Identification of Compounds for Butyrylcholinesterase Inhibition.
    Li S, Li AJ, Travers J, Xu T, Sakamuru S, Klumpp-Thomas C, Huang R, Xia M.
    SLAS Discov; 2021 Dec 01; 26(10):1355-1364. PubMed ID: 34269114
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  • 17. Differences in active-site gorge dimensions of cholinesterases revealed by binding of inhibitors to human butyrylcholinesterase.
    Saxena A, Redman AM, Jiang X, Lockridge O, Doctor BP.
    Chem Biol Interact; 1999 May 14; 119-120():61-9. PubMed ID: 10421439
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  • 18. Inhibition of acetylcholinesterase and butyrylcholinesterase by chlorpyrifos-oxon.
    Amitai G, Moorad D, Adani R, Doctor BP.
    Biochem Pharmacol; 1998 Aug 01; 56(3):293-9. PubMed ID: 9744565
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  • 19. Rivastigmine-Bambuterol Hybrids as Selective Butyrylcholinesterase Inhibitors.
    Wu J, Tan Z, Pistolozzi M, Tan W.
    Molecules; 2023 Dec 22; 29(1):. PubMed ID: 38202655
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  • 20. Proline-Based Carbamates as Cholinesterase Inhibitors.
    Pizova H, Havelkova M, Stepankova S, Bak A, Kauerova T, Kozik V, Oravec M, Imramovsky A, Kollar P, Bobal P, Jampilek J.
    Molecules; 2017 Nov 14; 22(11):. PubMed ID: 29135926
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