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PUBMED FOR HANDHELDS

Journal Abstract Search

64 related items for PubMed ID: 13283638

  • 1. [Differentiation of the cholinesterase activity of biological matter of various origins. II. Inhibitory effect of bis(piperidinomethyl cumaranil 5) ketone diiodomethylate (CT 3318)].
    PAULESU F, VARGIU L.
    Arch Int Pharmacodyn Ther; 1955 Nov 01; 104(1):11-8. PubMed ID: 13283638
    [No Abstract] [Full Text] [Related]

  • 2. [Specific anticholinesterase properties of bis(2,3-dihydro-2-piperidinomethyl-5-benzoturanyl) ketone dimethiodide (3318 CT). 1. Relation between chemical structure and anticholinesterase activity; inhibitory power in vitro and in vivo].
    JACOB J.
    Arch Int Pharmacodyn Ther; 1955 May 01; 101(4):446-68. PubMed ID: 13239238
    [No Abstract] [Full Text] [Related]

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  • 5. [Analgesic and anticholinesterase properties of the dihydrochloride and of the diiodomethylate of bis-(piperidonomethyl-coumaranyl-5) ketone].
    FUNKE A, JACOB J, VON DANIKEN K.
    C R Hebd Seances Acad Sci; 1953 Jan 05; 236(1):149-51. PubMed ID: 13033326
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  • 6. [Mouse tolerance of the analgesic action of morphine, 3204 [bis(2-piperidinomethyl-5-coumaranyl) ketone dihydrochloride] and of combined morphine and 3204 CT].
    JACOB J, ECHINARD-GARIN P.
    J Physiol (Paris); 1956 Jan 05; 48(3):576-80. PubMed ID: 13346566
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  • 7. Acetylcholinesterase inhibition by the ketone transition state analog phenoxyacetone and 1-halo-3-phenoxy-2-propanones.
    Dafforn A, Neenan JP, Ash CE, Betts L, Finke JM, Garman JA, Rao M, Walsh K, Williams RR.
    Biochem Biophys Res Commun; 1982 Jan 29; 104(2):597-602. PubMed ID: 7073703
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  • 8. [Significance of cholinesterase inhibition by in vitro manifestation of various effects of a specific inhibitor, bis(2,3-dihydro-2-piperidinomethy1-5-benzofuranyl) ketone dimethiodide (CT-3318)].
    ZANDA CE.
    Arch Int Pharmacodyn Ther; 1959 May 01; 120(1):53-63. PubMed ID: 13662037
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  • 13. Augmentation of atropine resistant spasms in plexus-containing guinea-pig longitudinal muscle by ganglionic action of the acetylcholinesterase inhibitor BW 284C51 (1:5 bis (p-allyl-dimethylammonium phenyl)-pentan-3-one dibromide).
    Ambache N, Zar MA.
    Br J Pharmacol; 1971 Aug 01; 42(4):657P-658P. PubMed ID: 5116052
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  • 14. Tertiary amine derivatives of chlorochalcone as acetylcholinesterase (AChE) and buthylcholinesterase (BuChE) inhibitors: the influence of chlorine, alkyl amine side chain and α,β-unsaturated ketone group.
    Gao XH, Zhou C, Liu HR, Liu LB, Tang JJ, Xia XH.
    J Enzyme Inhib Med Chem; 2017 Dec 01; 32(1):146-152. PubMed ID: 27801600
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  • 16. Synthesis and structure-activity relationships for biphenyl H3 receptor antagonists with moderate anti-cholinesterase activity.
    Morini G, Comini M, Rivara M, Rivara S, Bordi F, Plazzi PV, Flammini L, Saccani F, Bertoni S, Ballabeni V, Barocelli E, Mor M.
    Bioorg Med Chem; 2008 Dec 01; 16(23):9911-24. PubMed ID: 18976927
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  • 17. A novel series of potent and selective ketone histone deacetylase inhibitors with antitumor activity in vivo.
    Jones P, Altamura S, De Francesco R, Paz OG, Kinzel O, Mesiti G, Monteagudo E, Pescatore G, Rowley M, Verdirame M, Steinkühler C.
    J Med Chem; 2008 Apr 24; 51(8):2350-3. PubMed ID: 18370373
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  • 18. MIF tautomerase inhibitor potency of alpha,beta-unsaturated cyclic ketones.
    Garai J, Molnár V, Eros D, Orfi L, Lóránd T.
    Int Immunopharmacol; 2007 Dec 15; 7(13):1741-6. PubMed ID: 17996684
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