Engineered Biosynthesis of Antiprotealide and Other Unnatural Salinosporamide Proteasome Inhibitors-Reference-Cited by-同舟云学术

Engineered Biosynthesis of Antiprotealide and Other Unnatural Salinosporamide Proteasome Inhibitors

Published:2008-05-31 Issue:25 Volume:130 Page:7822-7823
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

McGlinchey Ryan P.¹,Nett Markus¹,Eustáquio Alessandra S.¹,Asolkar Ratnakar N.¹,Fenical William¹,Moore Bradley S.¹

Affiliation:

1. Scripps Institution of Oceanography and the Skaggs School of Pharmacy and Pharmaceutical Sciences, University of California at San Diego, La Jolla, California 92093

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja8029398

Reference19 articles.

1. An Efficient, Stereocontrolled Synthesis of a Potent Omuralide−Salinosporin Hybrid for Selective Proteasome Inhibition

2. Salinosporamide A: A Highly Cytotoxic Proteasome Inhibitor from a Novel Microbial Source, a Marine Bacterium of the New Genus Salinospora

3. A novel proteasome inhibitor NPI-0052 as an anticancer therapy

4. Total Synthesis and Biological Activity of Lactacystin, Omuralide and Analogs.

5. Crystal Structures of Salinosporamide A (NPI-0052) and B (NPI-0047) in Complex with the 20S Proteasome Reveal Important Consequences of β-Lactone Ring Opening and a Mechanism for Irreversible Binding

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