The isoquinoline derivative KN-62 a potent antagonist of the P2Z-receptor of human lymphocytes
Author:
Publisher
Wiley
Subject
Pharmacology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1038/sj.bjp.0701081/fullpdf
Reference39 articles.
1. Bound and determined: A computer program for making buffers of defined ion concentrations;BROOKS;Anal. Biochem.,1992
2. PPADS: an antagonist at endothelial P2Y-purinoceptors but not P2U-purinoceptors;BROWN;Br. J. Pharmacol.,1995
3. ATP induces nucleotide permeability in rat mast cells;COCKCROFT;Nature,1979
4. Pharmacological and biochemical analysis of FPL 67156, a novel, selective inhibitor of ecto-ATPase;CRACK;Br. J. Pharmacol.,1995
Cited by 178 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. Unlocking the therapeutic potential of P2X7 receptor: a comprehensive review of its role in neurodegenerative disorders;Frontiers in Pharmacology;2024-07-30
2. Ionotropic purinergic receptor 7 (P2X7) channel structure and pharmacology provides insight regarding non-nucleotide agonism;Channels;2024-05-19
3. Structure-Activity Relationships and Therapeutic Potential of Purinergic P2X7 Receptor Antagonists;Current Medicinal Chemistry;2024-04
4. Leveraging the ATP‐P2X7 receptor signalling axis to alleviate traumatic CNS damage and related complications;Medicinal Research Reviews;2023-03-16
5. P2X receptors: Insights from the study of the domestic dog;Neuropharmacology;2023-02
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