Literature DB >> 12164222

Investigation of structure-activity relationship on 17-spirolactone derivatives: the electronic-topological approach.

Fatma Kandemirli1, Nesrin Tokay, Nataly M Shvets, Anatoly S Dimoglo.   

Abstract

Sixty steroid homologues belonging to a series of 17-spirolactone derivatives such as aldosterone antagonists were investigated by electronic-topological method (ETM). Activity features Ph1-Ph3 that also are called pharmacophores were revealed. The pharmacophore Ph1 consists of two oxygen atoms and four carbon atoms. The mineralocorticoid activity appeared to be affected by the distance between the two oxygen atoms. Features AP1-AP3 that are characteristic of inactive compounds (or anti-pharmacophores) were also revealed. Comparative analysis of molecules that include either pharmacophores or anti-pharmacophores was carried out.

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Year:  2002        PMID: 12164222     DOI: 10.1016/s0014-827x(02)01256-9

Source DB:  PubMed          Journal:  Farmaco        ISSN: 0014-827X


  2 in total

1.  The investigation of structure-activity relationships of tacrine analogues: electronic-topological method.

Authors:  Murat Saracoglu; Fatma Kandemirli
Journal:  Open Med Chem J       Date:  2008-08-06

2.  ETM-ANN approach application for thiobenzamide and quinolizidine derivatives.

Authors:  M Saracoglu; F Kandemirli; V Kovalishyn; T Arslan; E E Ebenso
Journal:  J Biomed Biotechnol       Date:  2010-09-07
  2 in total

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