Literature DB >> 7700963

Structural and electronic conditions for anticonvulsant activity of bicyclic hydantoin derivatives.

J Karolak-Wojciechowska1, W Kwiatkowski, K Kiec-Kononowicz.   

Abstract

A series of bicyclic derivatives based on 5,5-diphenylhydantoin (DPH) and/or 5-arylidene-hydantoin skeletons (BZH) are discussed as potential anticonvulsants. In preliminary pharmacological tests a few of these agents showed some anticonvulsant activities, like the parent DPH. The electronic parameters (molecular electrostatic potential, MEP, and dipole moment orientation) for the DPH molecule used as a model differed significantly from those calculated for the bicyclic molecules. These parameters were derived from semiempirical quantum chemistry calculations applying the PM3 method.

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Year:  1995        PMID: 7700963

Source DB:  PubMed          Journal:  Pharmazie        ISSN: 0031-7144            Impact factor:   1.267


  2 in total

1.  Synthesis and antiproliferative activity of substituted diazaspiro hydantoins: a structure-activity relationship study.

Authors:  C S Ananda Kumar; S B Benaka Prasad; K Vinaya; S Chandrappa; N R Thimmegowda; S R Ranganatha; Sanjay Swarup; K S Rangappa
Journal:  Invest New Drugs       Date:  2008-07-08       Impact factor: 3.850

2.  Mechanism, kinetics and selectivity of selenocyclization of 5-alkenylhydantoins: an experimental and computational study.

Authors:  Biljana M Šmit; Radoslav Z Pavlović; Dejan A Milenković; Zoran S Marković
Journal:  Beilstein J Org Chem       Date:  2015-10-07       Impact factor: 2.883

  2 in total

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