Synthesis, biological evaluation, and molecular modeling of 11H-indeno[1,2-b]quinoxalin-11-one derivatives and tryptanthrin-6-oxime as c-Jun N-terminal kinase inhibitors-Reference-Cited by-同舟云学术

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Synthesis, biological evaluation, and molecular modeling of 11H-indeno[1,2-b]quinoxalin-11-one derivatives and tryptanthrin-6-oxime as c-Jun N-terminal kinase inhibitors

Published:2019-01 Issue: Volume:161 Page:179-191
ISSN:0223-5234
Container-title:European Journal of Medicinal Chemistry
language:en
Short-container-title:European Journal of Medicinal Chemistry

Author:

Schepetkin Igor A.,Khlebnikov Andrei I.,Potapov Andrei S.^ORCID,Kovrizhina Anastasia R.,Matveevskaya Vladislava V.^ORCID,Belyanin Maxim L.,Atochin Dmitriy N.,Zanoza Svitlana O.,Gaidarzhy Nadiya M.,Lyakhov Sergiy A.,Kirpotina Liliya N.,Quinn Mark T.^ORCID

Funder

Pfizer Investigator Initiated Research

National Institutes of Health

USDA

National Institute of Food and Agriculture

Montana State University

Tomsk Polytechnic University

Russian Science Foundation

Ministry of Education and Science of the Russian Federation

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Pharmacology,General Medicine

Reference73 articles.

1. Protein kinase activation and myocardial ischemia/reperfusion injury;Armstrong;Cardiovasc. Res.,2004

2. The functional contrariety of JNK;Bode;Mol. Carcinog.,2007

3. c-Jun N-terminal kinase (JNK) signaling: recent advances and challenges;Bogoyevitch;Biochim. Biophys. Acta,2010

4. Salvage of ischemic myocardium: a focus on JNK;Duplain;Hypoxia and Exercise,2006

5. Selective interaction of JNK protein kinase isoforms with transcription factors;Gupta;EMBO J.,1996

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