Aspirin prodrugs: synthesis and hydrolysis of 2-acetoxybenzoate esters of various N-(hydroxyalkyl) amides-Reference-Cited by-同舟云学术

Aspirin prodrugs: synthesis and hydrolysis of 2-acetoxybenzoate esters of various N-(hydroxyalkyl) amides

Published:1988-06 Issue:1-3 Volume:44 Page:151-158
ISSN:0378-5173
Container-title:International Journal of Pharmaceutics
language:en
Short-container-title:International Journal of Pharmaceutics

Author:

Bundgaard Hans,Nielsen Niels Mørk,Buur Anders

Publisher

Elsevier BV

Subject

Pharmaceutical Science

Reference26 articles.

1. Physicochemical property modification strategies based on enzyme substrate specificities I: rationale, synthesis, and pharmaceutical properties of aspirin derivatives;Banerjee;J. Pharm. Sci.,1981

2. Physicochemical property modification strategies based on enzyme substrate specificities II: α-chymotrypsin hydrolysis of aspirin derivatives;Banerjee;J. Pharm. Sci.,1981

3. Physicochemical property modification strategies based on enzyme substrate specificities III: carboxypeptidase A hydrolysis of aspirin derivatives;Banerjee;J. Pharm. Sci.,1981

4. Prodrugs as drug delivery systems. 65. Hydrolysis of α-hydroxy- and α-acyloxy-N-benzoyl glycine derivatives and implications for the design of prodrugs of NH-acidic compounds;Bundgaard;Int. J. Pharm.,1987

5. Prodrugs as drug delivery systems. 74. Facile hydrolysis of N-(acyloxymethyl) amide derivatives and implications for the design of prodrugs of NH-acidic compounds and of carboxylic acids;Bundgaard;Acta Pharm. Suec.,1987

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