Exploring the Conformational and Biological Versatility of β-Turn-Modified Gramicidin S by Using Sugar Amino Acid Homologues that Vary in Ring Size-Reference-Cited by-全球学者库

Exploring the Conformational and Biological Versatility of β-Turn-Modified Gramicidin S by Using Sugar Amino Acid Homologues that Vary in Ring Size

Published:2011-03-01 Issue:14 Volume:17 Page:3995-4004
ISSN:0947-6539
Container-title:Chemistry - A European Journal
language:en
Short-container-title:Chem. Eur. J.

Author:

Knijnenburg Annemiek D.,Tuin Adriaan W.,Spalburg Emile,de Neeling Albert J.,Mars-Groenendijk Roos H.,Noort Daan,Otero José M.,Llamas-Saiz Antonio L.,van Raaij Mark J.,van der Marel Gijs A.,Overkleeft Herman S.,Overhand Mark

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/chem.201002895/fullpdf

Reference78 articles.

1. Carbohydrate-Based Mimetics in Drug Design: Sugar Amino Acids and Carbohydrate Scaffolds

2. Glycosaminosäuren und ihre Verwendung als Bausteine in der kombinatorischen Synthese sowie ihre Bedeutung für die Wirkstoff-Forschung

3. Glycosamino Acids: Building Blocks for Combinatorial Synthesis—Implications for Drug Discovery

4. Sugar Amino Acids and Their Uses in Designing Bioactive Molecules

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