Design, synthesis and evaluation of β-lactam antigenic peptide hybrids; unusual opening of the β-lactam ring in acidic media-Reference-Cited by-同舟云学术

Design, synthesis and evaluation of β-lactam antigenic peptide hybrids; unusual opening of the β-lactam ring in acidic media

Published:2010 Issue:23 Volume:8 Page:5345
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Tarbe Marion,Azcune Itxaso,Balentová Eva,Miles John J.,Edwards Emily E.,Miles Kim M.,Do Priscilla,Baker Brian M.,Sewell Andrew K.,Aizpurua Jesus M.,Douat-Casassus Céline,Quideau Stéphane

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2010/OB/C003877F

Reference43 articles.

1. β-Turn mimetic library synthesis: scaffolds and applications

2. Bioactive Conformation of Luteinizing Hormone-Releasing Hormone: Evidence from a Conformationally Constrained Analog

3. Design and Synthesis of Novel Bioactive Peptides and Peptidomimetics

4. Development of a New Family of Conformationally Restricted Peptides as Potent Nucleators of β-Turns. Design, Synthesis, Structure, and Biological Evaluation of a β-Lactam Peptide Analogue of Melanostatin

5. Synthesis of β-Lactam Scaffolds for Ditopic Peptidomimetics

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