Cyanobacterial Peptides as a Prototype for the Design of Potent β-Secretase Inhibitors and the Development of Selective Chemical Probes for Other Aspartic Proteases-Reference-Cited by-同舟云学术

Cyanobacterial Peptides as a Prototype for the Design of Potent β-Secretase Inhibitors and the Development of Selective Chemical Probes for Other Aspartic Proteases

Published:2012-11-26 Issue:23 Volume:55 Page:10749-10765
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Liu Yanxia¹,Zhang Wei¹²,Li Li³,Salvador Lilibeth A.¹,Chen Tiantian³,Chen Wuyan³,Felsenstein Kevin M.⁴,Ladd Thomas B.⁴,Price Ashleigh R.⁴,Golde Todd E.⁴,He Jianhua⁵,Xu Yechun³,Li Yingxia²,Luesch Hendrik¹

Affiliation:

1. Department of Medicinal Chemistry, University of Florida, Gainesville, Florida 32610, United States

2. School of Pharmacy, Fudan University, Shanghai 201203, China

3. Drug Discovery and Design Center, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, 555 Zuchongzhi Road, Shanghai 201203, China

4. Department of Neuroscience, Center for Translational Research in Neurodegenerative Disease, University of Florida, Gainesville, Florida 32610, United States

5. Shanghai Institute of Applied Physics, Chinese Academy of Sciences, Shanghai 201800, China

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/jm301630s

Reference51 articles.

1. Filamentous tropical marine cyanobacteria: a rich source of natural products for anticancer drug discovery

2. Chemodiversity in Freshwater and Terrestrial Cyanobacteria – A Source for Drug Discovery

3. Kempopeptins A and B, Serine Protease Inhibitors with Different Selectivity Profiles from a Marine Cyanobacterium, Lyngbya sp.

4. Lyngbyastatins 8–10, Elastase Inhibitors with Cyclic Depsipeptide Scaffolds Isolated from the Marine Cyanobacterium Lyngbya semiplena

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