New C4- and C1-derivatives of furo[3,4-c]pyridine-3-ones and related compounds: Evidence for site-specific inhibition of the constitutive proteasome and its immunoisoform-Reference-Cited by-同舟云学术

New C4- and C1-derivatives of furo[3,4-c]pyridine-3-ones and related compounds: Evidence for site-specific inhibition of the constitutive proteasome and its immunoisoform

Published:2014-03 Issue:6 Volume:24 Page:1571-1580
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Hovhannisyan Anna,Pham The Hien,Bouvier Dominique,Piroyan Alexander,Dufau Laure,Qin Lixian,Cheng Yan,Melikyan Gagik,Reboud-Ravaux Michèle,Bouvier-Durand Michelle

Funder

French Association against myopathies

Publisher

Elsevier BV

Subject

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

Reference47 articles.

1. C1 and N5 derivatives of cerpegin: Synthesis of a new series based on structure–activity relationships to optimize their inhibitory effect on 20S proteasome

2. 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

3. Exploiting nature's rich source of proteasome inhibitors as starting points in drug development

4. Proteasome Inhibitors: An Expanding Army Attacking a Unique Target

5. Proteasome Inhibitors: Recent Advances and New Perspectives In Medicinal Chemistry

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4. The synthesis of novel 1-hetarylmethylidene-4-sulfanylfuro-[3,4-c]pyridin-3(1H)-ones;Chemistry of Heterocyclic Compounds;2022-09

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