机构

• 上海药物研究所 [30]

采集方式

• OAI收割 [30]

内容类型

• 期刊论文 [30]

发表日期

• 2023 [4]
• 2022 [2]
• 2021 [1]
• 2020 [1]
• 2018 [3]
• 2017 [1]
• 更多

学科主题

• Biochemist... [2]
• Life Scien... [1]

筛选

浏览/检索结果: 共30条，第1-10条 帮助 限定条件 专题：上海药物研究所    第一署名单位    第一作者单位    通讯作者单位     条数/页： 5101520253035404550556065707580859095100 排序方式： 请选择提交时间升序提交时间降序发表日期升序发表日期降序题名升序题名降序作者升序作者降序 Physiological and Pathological Functions of TRPM7 Channel and Its Small-molecule Modulators 期刊论文  OAI收割 PROGRESS IN BIOCHEMISTRY AND BIOPHYSICS, 2023, 卷号: 50, 期号: 12, 页码: 2856-2868 作者:  Wang, Yun-Qi;  Guan, Zi-Yue;  Gao, Zhao-Bing;  Zheng, Yue-Ming   |  收藏  |  浏览/下载：11/0  |  提交时间：2024/04/09 TRPM7  ion channel  physiological function  disease  small molecule modulators   TRP (transient receptor potential) ion channel family: structures, biological functions and therapeutic interventions for diseases 期刊论文  OAI收割 SIGNAL TRANSDUCTION AND TARGETED THERAPY, 2023, 卷号: 8, 期号: 1, 页码: 38 作者:  Zhang, Miao;  Ma, Yueming;  Ye, Xianglu;  Zhang, Ning;  Pan, Lei   |  收藏  |  浏览/下载：19/0  |  提交时间：2023/10/17 Discovery of selective NaV1.8 inhibitors based on 5-chloro-2-(4,4-difluor- oazepan-1-yl)-6-methyl nicotinamide scaffold for the treatment of pain 期刊论文  OAI收割 EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2023, 卷号: 254, 页码: 12 作者:  Qin, Hui;  Wei, Aihuan;  Wang, Yunqi;  Wang, Linlin;  Xu, Haiyan   |  收藏  |  浏览/下载：14/0  |  提交时间：2023/10/17 Pain  Non-addictive analgesics  Na V 1  8-selective inhibitors  Bicyclic aromatic groups   Naphthylisoquinoline alkaloids, a new structural template inhibitor of Nav1.7 sodium channel 期刊论文  OAI收割 ACTA PHARMACOLOGICA SINICA, 2023, 页码: 9 作者:  Wang, Qiao-qiao;  Wang, Long;  Zhang, Wen-bo;  Tang, Chun-ping;  Chen, Xue-qin   |  收藏  |  浏览/下载：20/0  |  提交时间：2023/10/17 Nav1.7 channel  naphthylisoquinolines  Ancistrocladus tectorius  dorsal root ganglion neurons  formalin-induced mouse inflammatory pain model  analgesics   Molecular Determinants for the High-Affinity Blockade of Human Ether-a-go-go-Related Gene K+ Channel by Tolterodine 期刊论文  OAI收割 JOURNAL OF CARDIOVASCULAR PHARMACOLOGY, 2022, 卷号: 80, 期号: 5, 页码: 679-689 作者:  Wang, Na;  Yang, Yang;  Wen, Jing;  Fan, Xin-Rong;  Li, Jian   |  收藏  |  浏览/下载：26/0  |  提交时间：2022/12/13 tolterodine  hERG channel  molecular docking  muscarinic acetylcholine receptor  tachycardia  overactive bladder   SCN8A epileptic encephalopathy mutations display a gain-of-function phenotype and divergent sensitivity to antiepileptic drugs 期刊论文  OAI收割 ACTA PHARMACOLOGICA SINICA, 2022, 页码: 10 作者:  Guo, Qian-bei;  Zhan, Li;  Xu, Hai-yan;  Gao, Zhao-bing;  Zheng, Yue-ming   |  收藏  |  浏览/下载：36/0  |  提交时间：2022/08/30 early infantile epileptic encephalopathy type 13  SCN8A  gain-of-function mutation  antiepileptic drugs  phenytoin  carbamazepine   Dual-Channel Fluorescent Probe for the Simultaneous Monitoring of Peroxynitrite and Adenosine-5 '-triphosphate in Cellular Applications 期刊论文  OAI收割 JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2021, 页码: 10 作者:  Wu, Luling;  Liu, Jihong;  Tian, Xue;  Groleau, Robin R.;  Feng, Beidou   |  收藏  |  浏览/下载：37/0  |  提交时间：2022/06/15 Discovery of aryl sulfonamide-selective Nav1.7 inhibitors with a highly hydrophobic ethanoanthracene core 期刊论文  OAI收割 ACTA PHARMACOLOGICA SINICA, 2020, 卷号: 41, 期号: 3, 页码: 293-302 作者:  Wang, Jin-tao;  Zheng, Yue-ming;  Chen, Yue-ting;  Gu, Min;  Gao, Zhao-bing   |  收藏  |  浏览/下载：30/0  |  提交时间：2020/07/01 Nav1  7 sodium channel  aryl sulfonamide  maprotiline  compound 10o  electrophysiology  acetic acid-induced visceral pain  analgesic activity   A binding-block ion selective mechanism revealed by a Na/K selective channel 期刊论文  OAI收割 PROTEIN & CELL, 2018, 卷号: 9, 期号: 7, 页码: 629-639 作者:  Yu, Jie;  Zhang, Bing;  Zhang, Yixiao   |  收藏  |  浏览/下载：35/0  |  提交时间：2019/01/08 cryo-EM  MscS  Na+/K+ selective channel   Enhancing inactivation rather than reducing activation of Nav1.7 channels by a clinically effective analgesic CNV1014802 期刊论文  OAI收割 ACTA PHARMACOLOGICA SINICA, 2018, 卷号: 39, 期号: 4, 页码: 587-596 作者:  Zheng, Yue-ming;  Wang, Wan-fu;  Li, Yan-fen;  Yu, Yong;  Gao, Zhao-bing   |  收藏  |  浏览/下载：50/0  |  提交时间：2019/01/08 Nav1.7 channels  analgesics  CNV1014802  inactivated state  paroxysmal extreme pain disorder