A new series of N5 derivatives of the 1,1,5-trimethyl furo[3,4-c]pyridine-3,4-dione (cerpegin) selectively inhibits the post-acid activity of mammalian 20S proteasomes-Reference-Cited by-同舟云学术

A new series of N5 derivatives of the 1,1,5-trimethyl furo[3,4-c]pyridine-3,4-dione (cerpegin) selectively inhibits the post-acid activity of mammalian 20S proteasomes

Published:2012-06 Issue:11 Volume:22 Page:3822-3827
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Pham The Hien,Hovhannisyan Anna,Bouvier Dominique,Tian Lei,Reboud-Ravaux Michèle,Melikyan Gagik,Bouvier-Durand Michelle

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

Reference46 articles.

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4. Esanu, A. U.S. Patent 4,585,776, 1986.

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