Literature DB >> 3598887

Anticonvulsant activity of indanylspirosuccinimide Mannich bases.

M R Borenstein, P H Doukas.   

Abstract

A series of Mannich bases derived from spiro [indan-1,3'pyrrolidine-2',5'-dione] were evaluated for anticonvulsant activity. This activity varied as a function of the amine substituent and several compounds showed protective effects in both the maximal electroshock (MES) and subcutaneous pentylenetetrazol (scMet) assays. In addition, fluorenyl- and cyclopentyl-derived spirosuccinimides, as well as extended chain analogues, were tested and proved to be inactive. A time versus effect study was conducted employing the MES assay and the hydroxyethylpiperazine-derived Mannich base of spiro [indan-1,3 pyrrolidine-2',5',dione]. This compound acted rapidly and its protective half-life was increased as larger doses were administered.

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Year:  1987        PMID: 3598887     DOI: 10.1002/jps.2600760407

Source DB:  PubMed          Journal:  J Pharm Sci        ISSN: 0022-3549            Impact factor:   3.534


  2 in total

1.  Synthesis, Cytotoxic Analysis, and Molecular Docking Studies of Tetrazole Derivatives via N-Mannich Base Condensation as Potential Antimicrobials.

Authors:  Ashraf Atef Hatamleh; Dunia Al Farraj; Sarah Salah Al-Saif; SathishKumar Chidambaram; Surendrakumar Radhakrishnan; Idhayadhulla Akbar
Journal:  Drug Des Devel Ther       Date:  2020-10-23       Impact factor: 4.162

2.  Synthesis of 1-Aryl-3-phenethylamino-1-propanone hydrochlorides as possible potent cytotoxic agents.

Authors:  Ebru Mete; Halise Inci Gul; Cavit Kazaz
Journal:  Molecules       Date:  2007-12-12       Impact factor: 4.411

  2 in total

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