Zhao-Bing Gao

Affiliations: 
Johns Hopkins University School of Medicine, Baltimore, MD, United States 
Area:
Ion channels
Google:
"Zhao-Bing Gao"
Mean distance: 15.37 (cluster 6)
 
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Publications

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Wang QQ, Wang L, Zhang WB, et al. (2023) Naphthylisoquinoline alkaloids, a new structural template inhibitor of Nav1.7 sodium channel. Acta Pharmacologica Sinica
Guo QB, Zhan L, Xu HY, et al. (2022) SCN8A epileptic encephalopathy mutations display a gain-of-function phenotype and divergent sensitivity to antiepileptic drugs. Acta Pharmacologica Sinica
Liu LX, Gu RR, Jin Y, et al. (2022) Diversity-oriented synthesis of marine polybrominated diphenyl ethers as potential KCNQ potassium channel activators. Bioorganic Chemistry. 126: 105909
Wang Y, Fang S, Wu Y, et al. (2021) Discovery of SARS-CoV-2-E channel inhibitors as antiviral candidates. Acta Pharmacologica Sinica
Xie ZQ, Tian XT, Zheng YM, et al. (2020) Antiepileptic geissoschizine methyl ether is an inhibitor of multiple neuronal channels. Acta Pharmacologica Sinica
Liao P, Qiu Y, Mo Y, et al. (2019) Selective activation of TWIK-related acid-sensitive K 3 subunit-containing channels is analgesic in rodent models. Science Translational Medicine. 11
Wang JT, Zheng YM, Chen YT, et al. (2019) Discovery of aryl sulfonamide-selective Nav1.7 inhibitors with a highly hydrophobic ethanoanthracene core. Acta Pharmacologica Sinica
Tian F, Qiu Y, Lan X, et al. (2019) A small molecular compound selectively activates K2P channel TASK-3 by acting at two distant clusters of residues. Molecular Pharmacology
Wang L, Qiao GH, Hu HN, et al. (2019) Discovery of Novel Retigabine Derivatives as Potent KCNQ4 and KCNQ5 Channel Agonists with Improved Specificity. Acs Medicinal Chemistry Letters. 10: 27-33
Rodier E, Niday Z, Doci K, et al. (2018) Inhibition of KCNQ2/3 channels by HN38 and XE991 depends on the conformation of the outer vestibule. Molecular Pharmacology
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