Literature DB >> 6771384

Use of molecular negentropy to encode structure governing biological activity.

L B Kier.   

Abstract

A drug molecule is considered to be an information source with an information content available to receptive tissue. In nonspecific interactions, much of the information content has quality as judged by the receptor. Quantitation of the information content using Shannon's equation gives the molecular negentropy. This index is shown to rank molecules according to symmetry and to encode structural characteristics influencing physical properties and biological activity in certain cases.

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Year:  1980        PMID: 6771384     DOI: 10.1002/jps.2600690717

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


  6 in total

1.  Theoretical descriptors for the quantitative rationalisation of plastocyanin mutant functional propertiess.

Authors:  F De Rienzo; G H Grant; M C Menziani
Journal:  J Comput Aided Mol Des       Date:  2002-07       Impact factor: 3.686

2.  Comparative QSPR studies with molecular connectivity, molecular negentropy and TAU indices. Part I: molecular thermochemical properties of diverse functional acyclic compounds.

Authors:  Kunal Roy; Achintya Saha
Journal:  J Mol Model       Date:  2003-06-20       Impact factor: 1.810

3.  On the information expressed in enzyme primary structure: lessons from Ribonuclease A.

Authors:  Daniel J Graham; Jessica L Greminger
Journal:  Mol Divers       Date:  2009-11-17       Impact factor: 2.943

4.  2D QSAR Studies of Several Potent Aminopyridine, Anilinopyrimidine and Pyridine Carboxamide-based JNK Inhibitors.

Authors:  S Sharma; B Bagchi; S Mukhopadhyay; A K Bothra
Journal:  Indian J Pharm Sci       Date:  2011-03       Impact factor: 0.975

5.  Prediction of multi-target networks of neuroprotective compounds with entropy indices and synthesis, assay, and theoretical study of new asymmetric 1,2-rasagiline carbamates.

Authors:  Francisco J Romero Durán; Nerea Alonso; Olga Caamaño; Xerardo García-Mera; Matilde Yañez; Francisco J Prado-Prado; Humberto González-Díaz
Journal:  Int J Mol Sci       Date:  2014-09-24       Impact factor: 5.923

6.  Some QSAR studies for a group of sulfonamide Schiff base as carbonic anhydrase CA II inhibitors.

Authors:  Erol Eroglu
Journal:  Int J Mol Sci       Date:  2008-02-26       Impact factor: 6.208

  6 in total

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