Bridged Analogues for p53-Dependent Cancer Therapy Obtained by S-Alkylation-Reference-Cited by-同舟云学术

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Bridged Analogues for p53-Dependent Cancer Therapy Obtained by S-Alkylation

Published:2015-08-19 Issue:1 Volume:22 Page:67-81
ISSN:1573-3149
Container-title:International Journal of Peptide Research and Therapeutics
language:en
Short-container-title:Int J Pept Res Ther

Author:

Micewicz Ewa D.,Sharma Shantanu,Waring Alan J.,Luong Hai T.,McBride William H.,Ruchala Piotr

Funder

National Institute of Allergy and Infectious Diseases (US)

Publisher

Springer Science and Business Media LLC

Subject

Drug Discovery,Molecular Medicine,Biochemistry,Bioengineering,Analytical Chemistry

Link

http://link.springer.com/content/pdf/10.1007/s10989-015-9487-3.pdf

Reference151 articles.

1. Almeida AM, Li R, Gellman SH (2012) Parallel beta-sheet secondary structure is stabilized and terminated by interstrand disulfide cross-linking. J Am Chem Soc 134:75–78

2. Angelini A, Cendron L, Chen S et al (2012a) Bicyclic peptide inhibitor reveals large contact interface with a protease target. ACS Chem Biol 7:817–821

3. Angelini A, Diderich P, Morales-Sanfrutos J et al (2012b) Chemical macrocyclization of peptides fused to antibody Fc fragments. Bioconjug Chem 23:1856–1863

4. Angelini A, Morales-Sanfrutos J, Diderich P, Chen S, Heinis C (2012c) Bicyclization and tethering to albumin yields long-acting peptide antagonists. J Med Chem 55:10187–10197

5. Baeriswyl V, Heinis C (2013a) Phage selection of cyclic peptide antagonists with increased stability toward intestinal proteases. Protein Eng Des Sel 26:81–89

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