Syntheses and structure–activity relationships for some triazolyl p38α MAPK inhibitors-Reference-Cited by-同舟云学术

Syntheses and structure–activity relationships for some triazolyl p38α MAPK inhibitors

Published:2014-03 Issue:5 Volume:24 Page:1352-1357
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Seerden Jean-Paul G.,Leusink-Ionescu Gabriela,Leguijt Robin,Saccavini Catherine,Gelens Edith,Dros Bas,Woudenberg-Vrenken Titia,Molema Grietje,Kamps Jan A.A.M.,Kellogg Richard M.

Publisher

Elsevier BV

Subject

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

Reference43 articles.

1. Laufer, S.; Margutti, S. Medicinal Chemistry Approaches for the Inhibition of the p38 MAPK Pathway. In: Protein Kinases as Drug Targets, Klebl, B., Müller, G., Hamacher, M., Eds.; Methods and Principles in Medicinal chemistry, Wiley-VCH, 2011; Vol. 49, Chapter 9, pp 271–304.

2. Pharmacophore Design of p38α MAP Kinase Inhibitors with Either 2,4,5-Trisubstituted or 1,2,4,5-Tetrasubstituted Imidazole Scaffold

3. Targeting kinases for the treatment of inflammatory diseases

4. p38MAPK: stress responses from molecular mechanisms to therapeutics

5. Successful Structure-Based Design of Recent p38 MAP Kinase Inhibitors

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