Literature DB >> 9923194

5-Arylidene-3-aryl-pyrrolidine-2,4-diones with affinity to the N-methyl-D-aspartate (glycine site) receptor, Part I.

H Poschenrieder1, G Höfner, H D Stachel.   

Abstract

A series of new 5-arylidene 3-aryl-pyrrolidine-2,4-diones has been prepared. Their binding affinity toward the N-methyl-D-aspartate (glycine site) receptor has been measured as a basis for more detailed structure-activity relationship studies.

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Year:  1998        PMID： 9923194     DOI： 10.1002/(sici)1521-4184(199812)331:12<389::aid-ardp389>3.0.co;2-w

Source DB:  PubMed          Journal:  Arch Pharm (Weinheim)        ISSN： 0365-6233            Impact factor:   3.751


  1 in total

1.  Ruthenium-catalyzed selective hydrogenation of bis-arylidene tetramic acids. Application to the synthesis of novel structurally diverse pyrrolidine-2,4-diones.

Authors:  Christos S Karaiskos; Dimitris Matiadis; John Markopoulos; Olga Igglessi-Markopoulou
Journal:  Molecules       Date:  2011-07-20       Impact factor: 4.411
  1 in total

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