Design and synthesis of potent, orally bioavailable dihydroquinazolinone inhibitors of p38 MAP kinase-Reference-Cited by-同舟云学术

Design and synthesis of potent, orally bioavailable dihydroquinazolinone inhibitors of p38 MAP kinase

Published:2003-01 Issue:2 Volume:13 Page:277-280
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Stelmach John E.,Liu Luping,Patel Sangita B.,Pivnichny James V.,Scapin Giovanna,Singh Suresh,Hop Cornelis E.C.A.,Wang Zhen,Strauss John R.,Cameron Patricia M.,Nichols Elizabeth A.,O'Keefe Stephen J.,O'Neill Edward A.,Schmatz Dennis M.,Schwartz Cheryl D.,Thompson Chris M.,Zaller Dennis M.,Doherty James B.

Publisher

Elsevier BV

Subject

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

Reference15 articles.

1. MAP Kinases

2. New inhibitors of p38 kinase

3. A highly specific inhibitor of human p38 MAP kinase binds in the ATP pocket

Cited by 86 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. How many kinases are druggable? A review of our current understanding;Biochemical Journal;2023-08-29

2. Novel Approaches for the Solid-Phase Synthesis of Dihydroquinazoline-2(1H)-One Derivatives and Biological Evaluation as Potential Anticancer Agents;Molecules;2022-12-05

3. Copper‐Catalyzed Synthesis of 5‐Arylindolo[1,2‐ c ]quinazolin‐6(5 H )‐ones from 2‐(2‐Bromoaryl)indoles and Aryl Isocyanates under Microwave Irradiation;European Journal of Organic Chemistry;2022-06-10

4. Cholinergic System and Its Therapeutic Importance in Inflammation and Autoimmunity;Frontiers in Immunology;2021-04-15

5. Synthesis of substituted 3,4-dihydroquinazolinones via a metal free Leuckart–Wallach type reaction;RSC Advances;2021