The identification of pyrazolo[1,5-a]pyridines as potent p38 kinase inhibitors-Reference-Cited by-同舟云学术

The identification of pyrazolo[1,5-a]pyridines as potent p38 kinase inhibitors

Published:2008-10 Issue:20 Volume:18 Page:5428-5430
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Cheung Mui,Harris Philip A.,Badiang Jennifer G.,Peckham Gregory E.,Chamberlain Stanley D.,Alberti Michael J.,Jung David K.,Harris Stephanie S.,Bramson Neal H.,Epperly Andrea H.,Stimpson Stephen A.,Peel Michael R.

Publisher

Elsevier BV

Subject

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

Reference11 articles.

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

2. Role of CSBP/p38/RK stress response kinase in LPS and cytokine signaling mechanisms

3. New Approaches to the Treatment of Inflammatory Disorders Small Molecule inhibitors of p38 MAP Kinase

4. Pathway to the Clinic: Inhibition of P38 MAP Kinase. A Review of Ten Chemotypes Selected for Development

5. Small molecular anti-cytokine agents

Cited by 43 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Synthetic and Pharmacological Expedition of Pyrazolo[1,5-a]pyridine: A Comprehensive Review;Letters in Drug Design & Discovery;2024-01

2. Synthesis of pyrazolo[5,1-a]isoquinolines via C–H/N–H annulation of pyrazoles and alkynes with ruthenium(II) catalysts;Monatshefte für Chemie - Chemical Monthly;2023-07-15

3. Green Synthetic Approach: A Well-organized Eco-friendly Tool for Synthesis of Bio-active Fused Heterocyclic Compounds;Current Green Chemistry;2023-04

4. Synthesis and Mechanistic Investigation of Bipyrazolo[1,5-a]pyridines via Palladium-Catalyzed Cross-Dehydrogenative Coupling of Pyrazolo[1,5-a]pyridines;The Journal of Organic Chemistry;2022-07-18

5. Surface Plasmon Resonance Screening to Identify Active and Selective Adenosine Receptor Binding Fragments;ACS Medicinal Chemistry Letters;2022-06-06