Continued exploration of the triazolopyridine scaffold as a platform for p38 MAP kinase inhibition-Reference-Cited by-同舟云学术

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Continued exploration of the triazolopyridine scaffold as a platform for p38 MAP kinase inhibition

Published:2010-01 Issue:2 Volume:20 Page:469-473
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Jerome Kevin D.,Rucker Paul V.,Xing Li,Shieh Huey S.,Baldus John E.,Selness Shaun R.,Letavic Michael A.,Braganza John F.,McClure Kim F.

Publisher

Elsevier BV

Subject

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

Reference22 articles.

1. p38 Inhibitors: beyond pyridinylimidazoles

2. A protein kinase involved in the regulation of inflammatory cytokine biosynthesis

3. Cytokines and cytokine inhibitors or antagonists in rheumatoid arthritis

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2. A green one-pot process for the synthesis of 1,2,4-triazole-fused heterocycles using FeBr3 catalyst and hydrogen peroxide;Tetrahedron;2023-11

3. Triazolopyridine, a leitmotif of synthetic methods and pharmacological attributes: An extensive review;Arabian Journal of Chemistry;2023-10

4. A review of synthetic methods of 1,2,4-triazolopyridines and their therapeutic properties;Results in Chemistry;2023-01

5. Construction of 1,2,4-triazole-fused heterocycles via an amine oxidase-inspired catalyst;Organic Chemistry Frontiers;2023

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