Prodrugs as drug delivery systems. XXX. 4-Imidazolidinones as potential bioreversible derivatives for the α-aminoamide moiety in peptides-Reference-Cited by-同舟云学术

Prodrugs as drug delivery systems. XXX. 4-Imidazolidinones as potential bioreversible derivatives for the α-aminoamide moiety in peptides

Published:1984-07 Issue:3 Volume:20 Page:273-284
ISSN:0378-5173
Container-title:International Journal of Pharmaceutics
language:en
Short-container-title:International Journal of Pharmaceutics

Author:

Klixbüll Ulla,Bundgaard Hans

Publisher

Elsevier BV

Subject

Pharmaceutical Science

Reference38 articles.

1. The reaction of aspartyl dipeptide enters with ketones;Ariyoshi;Bull. Chem. Soc. Jap.,1972

2. Hydrolysis and intramolecular aminolysis of cephalexin and cephaloglycin in aqueous solution;Bundgaard;Arch. Pharm. Chem., Sci. Edn.,1976

3. Novel bioreversible derivatives of amides, imides, ureides, amines and other chemical entities not readily derivaiizable;Bundgaard,1981

4. Prodrugs as drug delivery systems. IV. N-Mannich bases as potential novel prodrugs for amides, ureides, amines, and other NH-acidic compounds;Bundgaard;J. Pharm. Sci.,1980

5. Prodrugs as drug delivery systems. X. N-Mannich bases as novel prodrug candidates for amides, imides, urea derivatives, amines and other NH-acidic compounds. Kinetics and mechanisms of decomposition and structure-reactivity relationships;Bundgaard;Arch. Pharm. Chem., Sci. Edn.,1980

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