Design and synthesis of 6-anilinoindazoles as selective inhibitors of c-Jun N-terminal kinase-3-Reference-Cited by-同舟云学术

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Design and synthesis of 6-anilinoindazoles as selective inhibitors of c-Jun N-terminal kinase-3

Published:2005-11 Issue:22 Volume:15 Page:5095-5099
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Swahn Britt-Marie,Huerta Fernando,Kallin Elisabet,Malmström Jonas,Weigelt Tatjana,Viklund Jenny,Womack Patrick,Xue Yafeng,Öhberg Liselotte

Publisher

Elsevier BV

Subject

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

Reference25 articles.

1. Selective interaction of JNK protein kinase isoforms with transcription factors.

2. p493F12 kinase: A novel MAP kinase expressed in a subset of neurons in the human nervous system

3. Absence of excitotoxicity-induced apoptosis in the hippocampus of mice lacking the Jnk3 gene

4. A critical role of neural-specific JNK3 for ischemic apoptosis

5. JNK-mediated induction of cyclooxygenase 2 is required for neurodegeneration in a mouse model of Parkinson's disease

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