Synthesis and SAR of piperazine amides as novel c-jun N-terminal kinase (JNK) inhibitors-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Synthesis and SAR of piperazine amides as novel c-jun N-terminal kinase (JNK) inhibitors

Published:2009-06 Issue:12 Volume:19 Page:3344-3347
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Shin Youseung,Chen Weiming,Habel Jeff,Duckett Derek,Ling Yuan Yuan,Koenig Marcel,He Yuanjun,Vojkovsky Tomas,LoGrasso Philip,Kamenecka Theodore M.

Publisher

Elsevier BV

Subject

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

Reference27 articles.

1. The c-Jun N-terminal protein kinase family of mitogen-activated protein kinases (JNK MAPKs)

2. The JNK signal transduction pathway

3. Selective interaction of JNK protein kinase isoforms with transcription factors.

4. p493F12 kinase: A novel MAP kinase expressed in a subset of neurons in the human nervous system

5. Localization of the messenger RNA for the c-Jun NH2-terminal kinase kinase in the adult and developing rat brain: an in situ hybridization study

Cited by 25 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. In Vitro and In Silico Study to Assess Toxic Mechanisms of Hybrid Molecules of Quinone-Benzocaine as Plastoquinone Analogues in Breast Cancer Cells;ACS Omega;2022-08-15

2. Design and Synthesis of Novel Piperazine (2-Chloroethyl)-1-nitrosourea Analogues as Anticancer Agents;Asian Journal of Chemistry;2022

3. N-Aromatic-Substituted Indazole Derivatives as Brain-Penetrant and Orally Bioavailable JNK3 Inhibitors;ACS Medicinal Chemistry Letters;2021-09-21

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

5. Identification and neuroprotective evaluation of a potential c-Jun N-terminal kinase 3 inhibitor through structure-based virtual screening and in-vitro assay;Journal of Computer-Aided Molecular Design;2020-02-10

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线，采集、加工和组织学术论文而形成的新型学术文献查询和分析系统，可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容，当前同舟云学术共收录了国内外主流学术期刊6万余种，收集的期刊论文及会议论文总量共计约1.5亿篇，并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询！咨询电话：010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号京ICP备18003416号-3