Literature DB >> 671234

Controlled delivery of theophylline: chemistry of 7-acyl- and 7,7'-acylditheophylline derivates.

N Bodor, K B Sloan, Y N Kuo, T Higuchi.   

Abstract

7-Acyl- and 7,7'-acylditheophylline derivatives were prepared from the reaction of theophylline with acid chlorides. In addition, a novel synthesis of these compounds was developed, which proceeds through an acylonium ion generated under mild conditions. The physical properties and stability of the derivative of choice, 7,7'-succinylditheophylline, depend on the synthetic procedure employed. This compound is a useful controlled-release prodrug of theophylline.

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Year:  1978        PMID: 671234     DOI: 10.1002/jps.2600670806

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


  1 in total

1.  Adenosine receptor prodrugs: towards kidney-selective dialkylxanthines.

Authors:  S Barone; P C Churchill; K A Jacobson
Journal:  J Pharmacol Exp Ther       Date:  1989-07       Impact factor: 4.030

  1 in total

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