Prodrugs of peptides

Author:

Buur Anders,Bundgaard Hans

Publisher

Elsevier BV

Subject

Pharmaceutical Science

Reference35 articles.

1. Reaction of acylamino acids with paraformaldehyde;Ben-Ishai;J. Org. Chem.,1957

2. Design of prodrugs: bioreversible derivatives for various functional groups and chemical entities;Bundgaard,1985

3. Bioreversible derivatization of peptides;Bundgaard,1986

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

5. Prodrugs as drug delivery systems. 77. Phthalidyl derivatives as prodrug forms for amides, sulfonamides, carbamates and other NH-acidic compounds;Bundgaard;Int. J. Pharm.,1988

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1. Improving Membrane Permeation in the Beyond Rule-of-Five Space by Using Prodrugs to Mask Hydrogen Bond Donors;ACS Chemical Biology;2020-07-06

2. Synthesis of Constrained Peptidomimetics Containing 2-Oxo-1,3-oxazolidine-4-carboxylic Acids;European Journal of Organic Chemistry;2011-07-13

3. Oral Delivery of Proteins and Peptides;Challenges in Delivery of Therapeutic Genomics and Proteomics;2011

4. Metabolic Considerations in Prodrug Design;Burger's Medicinal Chemistry and Drug Discovery;2003-01-15

5. Modifying peptide properties by prodrug design for enhanced transport into the CNS;Peptide Transport and Delivery into the Central Nervous System;2003

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