Model prodrugs designed for the intestinal peptide transporter. A synthetic approach for coupling of hydroxy-containing compounds to dipeptides-Reference-Cited by-同舟云学术

Model prodrugs designed for the intestinal peptide transporter. A synthetic approach for coupling of hydroxy-containing compounds to dipeptides

Published:2001-08 Issue:1 Volume:14 Page:13-19
ISSN:0928-0987
Container-title:European Journal of Pharmaceutical Sciences
language:en
Short-container-title:European Journal of Pharmaceutical Sciences

Author:

Friedrichsen Gerda Marie,Nielsen Carsten Uhd,Steffansen Bente,Begtrup Mikael

Publisher

Elsevier BV

Subject

Pharmaceutical Science

Reference13 articles.

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2. Structural specificity of mucosal–cell transport and metabolism of peptide drugs: Implication for oral peptide drug delivery;Bai;Pharm. Res.,1992

3. Deamidation, isomerization, and racemization at asparaginyl and aspartyl residues in peptides;Geiger;J. Biol. Chem.,1987

4. Chemical pathways of peptide and protein degradation;Goolcharran,2000

5. Hansch, C., Leo, A., Hoekman, D., 1995. Exploring QSAR. In: Hydrophobic, electronic, and steric constants. American Chemical Society, USA, pp. 282–283.

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