Synthesis and biological evaluation of naphthoquinone analogs as a novel class of proteasome inhibitors-Reference-Cited by-同舟云学术

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Synthesis and biological evaluation of naphthoquinone analogs as a novel class of proteasome inhibitors

Published:2010-08 Issue:15 Volume:18 Page:5576-5592
ISSN:0968-0896
Container-title:Bioorganic & Medicinal Chemistry
language:en
Short-container-title:Bioorganic & Medicinal Chemistry

Author:

Lawrence Harshani R.,Kazi Aslamuzzaman,Luo Yunting,Kendig Robert,Ge Yiyu,Jain Sanjula,Daniel Kenyon,Santiago Daniel,Guida Wayne C.,Sebti Saïd M.

Funder

NIH

Publisher

Elsevier BV

Subject

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

Reference52 articles.

1. Structure of 20S proteasome from yeast at 2.4Å resolution

2. Crystal Structure of the Boronic Acid-Based Proteasome Inhibitor Bortezomib in Complex with the Yeast 20S Proteasome

3. The ubiquitin-mediated protein degradation pathway in cancer: therapeutic implications

4. Alternative UPS drug targets upstream the 26S proteasome

5. Cell cycle, proteolysis and cancer

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4. Efficient Synthesis of Fully Substituted and Diversely Functionalized Pyrazoles through p‐TSA Catalyzed One‐Pot Condensation of Cyclic β‐Diketones, Arylglyoxals and Arylhydrazones;European Journal of Organic Chemistry;2023-09-26

5. Design, synthesis, and biological evaluation of some novel naphthoquinone‐glycine/β‐alanine anilide derivatives as noncovalent proteasome inhibitors;Chemical Biology & Drug Design;2023-02-17

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