Literature DB >> 9871602

New bronchodilators selected by molecular topology.

I Ríos-Santamarina1, R García-Domenech, J Gálvez, J Cortijo, P Santamaria, E Morcillo.   

Abstract

Molecular topology has been applied to find new lead compounds with bronchodilator activity. Among the selected compounds stands out 3-(1H-tetrazol-5yl)-9H-thioxanthene-9 -one-10,10-dioxide, anthrarobin, 9-oxo-9H-thioxantene-3-carboxylic-10,10-dioxide acid, acenocoumarol and griseofulvin, with a percentage of relaxation, at 0.1 mM, of 91, 92, 85, 69, and 74%, respectively. Theophylline shows a correspondent value of 77% (Emax = 100% at 1 mM).

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Year:  1998        PMID: 9871602     DOI: 10.1016/s0960-894x(98)00056-0

Source DB:  PubMed          Journal:  Bioorg Med Chem Lett        ISSN: 0960-894X            Impact factor:   2.823


  2 in total

1.  Optimization of a mathematical topological pattern for the prediction of antihistaminic activity.

Authors:  M J Duart; R García-Domenech; G M Antón-Fos; J Gálvez
Journal:  J Comput Aided Mol Des       Date:  2001-06       Impact factor: 3.686

2.  QSAR studies on a number of pyrrolidin-2-one antiarrhythmic arylpiperazinyls.

Authors:  Alicja Nowaczyk; Katarzyna Kulig
Journal:  Med Chem Res       Date:  2011-01-07       Impact factor: 1.965

  2 in total

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