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Novel Potassium Channel Inhibitors
ACS Medicinal Chemistry Letters ( IF 4.2 ) Pub Date : 2020-11-23 , DOI: 10.1021/acsmedchemlett.0c00569
Benjamin E Blass 1
Affiliation  

Roach, K. M.; Bradding, P. Ca2+ signalling in fibroblasts and the therapeutic potential of KCa3.1 channel blockers in fibrotic diseases. Br. J. Pharmacol. 2020, 177 (5), 1003–1024. Manfroni, G.; Ragonese, F.; Monarca, L.; Astolfi, A.; Mancinelli, L.; Iannitti, R. G.; Bastioli, F.; Barreca, M. L.; Cecchetti, V.; Fioretti, B. New insights on KCa3.1 channel modulation. Curr. Pharm. Des. 2020, 26 (18), 2096–2101. Mohr, C. J.; Steudel, F. A.; Gross, D.; Ruth, P.; Lukowski, R.; Mohr, C. J.; Lo, W. Y.; Hoppe, R.; Schroth, W.; Brauch, H.; Huber, S. M “Cancer- Associated Intermediate Conductance Ca2+-Activated K+ Channel KCa3.1 Cancers 2019, 11, 1–22. The author declares no competing financial interest. The author declares no competing financial interest. This article has not yet been cited by other publications.

中文翻译:

新型钾通道抑制剂

罗奇,公里布拉丁,P.成纤维细胞中的Ca 2+信号传导和 K Ca 3.1 通道阻滞剂在纤维化疾病中的治疗潜力。兄弟 J. 药理学。 2020 , 177 (5), 1003–1024。曼弗罗尼,G拉贡内塞,F莫纳尔卡,L阿斯托尔菲,A曼奇内利,L扬尼蒂,RG巴斯蒂奥利,F巴雷卡,ML ; 切凯蒂,五; 菲奥雷蒂,B.关于 KCa3.1 通道调制的新见解。咖喱 医药。德。 2020 , 26 (18), 2096–2101。莫尔,CJ斯图德尔, FA ; 格罗斯,D露丝,P卢考斯基,R莫尔,CJ罗,怀霍普,R施罗斯,W布劳赫,H胡伯,S.M “癌症相关的中间电导 Ca 2+ -激活的 K +通道 K Ca 3.1癌症 201911 月1-22 日。作者声明没有竞争性经济利益。作者声明没有竞争性经济利益。这篇文章还没有被其他出版物引用。
更新日期:2020-12-10
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