Nichole Coleman, Ph.D.
Affiliations: | 2014 | Chemistry | University of California, Davis, Davis, CA |
Area:
Organic Chemistry, Medicine and SurgeryGoogle:
"Nichole Coleman"Mean distance: (not calculated yet)
Parents
Sign in to add mentorHeike Wulff | grad student | 2014 | UC Davis | |
(The Design, Synthesis and Functional in-vivo Evaluation of Potent and Selective Small Molecules Targeting KCa Channels.) |
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Publications
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Oliván-Viguera A, Valero MS, Pinilla E, et al. (2016) Vascular reactivity profile of novel KC a 3.1-selective positive-gating modulators in the coronary vascular bed. Basic & Clinical Pharmacology & Toxicology |
Oliván-Viguera A, Valero MS, Coleman N, et al. (2015) A novel pan-negative-gating modulator of KCa2/3 channels, fluoro-di-benzoate, RA-2, inhibits endothelium-derived hyperpolarization-type relaxation in coronary artery and produces bradycardia in vivo. Molecular Pharmacology. 87: 338-48 |
Coleman N, Nguyen HM, Cao Z, et al. (2015) The riluzole derivative 2-amino-6-trifluoromethylthio-benzothiazole (SKA-19), a mixed KCa2 activator and NaV blocker, is a potent novel anticonvulsant. Neurotherapeutics : the Journal of the American Society For Experimental Neurotherapeutics. 12: 234-49 |
Brown BM, Coleman N, Yarov-Yarovoy V, et al. (2015) Positive KCa Channel Gating Modulators with Selectivity for KCa3.1 Biophysical Journal. 108: 20a |
Coleman N, Brown BM, Oliván-Viguera A, et al. (2014) New positive Ca2+-activated K+ channel gating modulators with selectivity for KCa3.1. Molecular Pharmacology. 86: 342-57 |
Lam J, Coleman N, Garing AL, et al. (2013) The therapeutic potential of small-conductance KCa2 channels in neurodegenerative and psychiatric diseases. Expert Opinion On Therapeutic Targets. 17: 1203-20 |
Strøbæk D, Brown DT, Jenkins DP, et al. (2013) NS6180, a new K(Ca) 3.1 channel inhibitor prevents T-cell activation and inflammation in a rat model of inflammatory bowel disease. British Journal of Pharmacology. 168: 432-44 |
Bodendiek SB, Rubinos C, Trelles MP, et al. (2012) Triarylmethanes, a new class of cx50 inhibitors. Frontiers in Pharmacology. 3: 106 |