Structure-driven HtL: Design and synthesis of novel aminoindazole inhibitors of c-Jun N-terminal kinase activity-Reference-Cited by-同舟云学术

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Structure-driven HtL: Design and synthesis of novel aminoindazole inhibitors of c-Jun N-terminal kinase activity

Published:2005-07 Issue:14 Volume:15 Page:3459-3462
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Stocks Michael J.,Barber Simon,Ford Rhonan,Leroux Frederic,St-Gallay Steve,Teague Simon,Xue Yafeng

Publisher

Elsevier BV

Subject

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

Reference25 articles.

1. Mitogen-activated protein kinases in chronic intestinal inflammation - targeting ancient pathways to treat modern diseases

2. Mitogen-Activated Protein Kinase Pathways Mediated by ERK, JNK, and p38 Protein Kinases

3. Inhibition of Cell Proliferation and Cell Cycle Progression by Specific Inhibition of Basal JNK Activity

4. Prolactin-induced Cell Proliferation in PC12 Cells Depends on JNK but Not ERK Activation

5. The c-Jun amino-terminal kinase pathway is preferentially activated by interleukin-1 and controls apoptosis in differentiating pancreatic beta-cells.

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2. Recent Advances in c-Jun N-Terminal Kinase (JNK) Inhibitors;Current Medicinal Chemistry;2021-02-01

3. C-Jun N-terminal kinase inhibitors: Structural insight into kinase-inhibitor complexes;Computational and Structural Biotechnology Journal;2020

4. A nonparametric weighted feature extraction-based method for c-Jun N-terminal kinase-3 inhibitor prediction;Journal of Molecular Graphics and Modelling;2019-07

5. Substituent Effects of 2-Pyridones on Selective O-Arylation with Diaryliodonium Salts: Synthesis of 2-Aryloxypyridines under Transition-Metal-Free Conditions;Synthesis;2018-01-24

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