Prodrugs as drug delivery systems. XXX. 4-Imidazolidinones as potential bioreversible derivatives for the α-aminoamide moiety in peptides
- 1 July 1984
- journal article
- research article
- Published by Elsevier in International Journal of Pharmaceutics
- Vol. 20 (3) , 273-284
- https://doi.org/10.1016/0378-5173(84)90174-1
Abstract
No abstract availableThis publication has 29 references indexed in Scilit:
- Peptides and the blood-brain barrierLife Sciences, 1983
- Mechanism of hydrolysis of N-(1-aminoalkyl)amidesJournal of the American Chemical Society, 1981
- ‘Acetaldehyde-enkephalins’: elucidation of the structure of the acetaldehyde adducts of methionine-enkephalin and leucine-enkephalinFEBS Letters, 1980
- Kinetic approach to the development in .BETA.-lactam antibiotics. II. Prodrug. I. Simultaneous determination of hetacillin and ampicillin, and its application to the stability of hetacillin in aqueous solution.CHEMICAL & PHARMACEUTICAL BULLETIN, 1974
- N, N′‐Alkylidenpeptide: Peptidsynthese‐Nebenprodukte bei Einwirkung von CarbonylverbindungenHelvetica Chimica Acta, 1973
- The Reaction of Aspartyl Dipeptide Esters with KetonesBulletin of the Chemical Society of Japan, 1972
- Condensation of aldehydes and ketones with dipeptidesThe Journal of Organic Chemistry, 1972
- The equilibrium between the antibiotics hetacillin and ampicillin in solutionJournal of the Chemical Society D: Chemical Communications, 1970
- Structure of acetone-oxytocin with studies on the reaction of acetone with various peptidesJournal of the American Chemical Society, 1968
- Synthesis of acetone-oxytocin from an isopropylidene derivative of S-benzyl-L-cysteinyl-L-tyrosineJournal of the American Chemical Society, 1968