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Highly potent and selective NaV1.7 inhibitors for use as intravenous agents and chemical probes.
Bioorg Med Chem Lett. 2017 Nov 1;27(21):4805-4811. doi: 10.1016/j.bmcl.2017.09.056. Epub 2017 Sep 28.
Bioorg Med Chem Lett. 2017.
PMID: 29029933
Discovery of Allosteric, Potent, Subtype Selective, and Peripherally Restricted TrkA Kinase Inhibitors.
Bagal SK, Omoto K, Blakemore DC, Bungay PJ, Bilsland JG, Clarke PJ, Corbett MS, Cronin CN, Cui JJ, Dias R, Flanagan NJ, Greasley SE, Grimley R, Johnson E, Fengas D, Kitching L, Kraus ML, McAlpine I, Nagata A, Waldron GJ, Warmus JS.
Bagal SK, et al. Among authors: fengas d.
J Med Chem. 2019 Jan 10;62(1):247-265. doi: 10.1021/acs.jmedchem.8b00280. Epub 2018 May 3.
J Med Chem. 2019.
PMID: 29672039
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The discovery and optimization of benzimidazoles as selective NaV1.8 blockers for the treatment of pain.
Brown AD, Bagal SK, Blackwell P, Blakemore DC, Brown B, Bungay PJ, Corless M, Crawforth J, Fengas D, Fenwick DR, Gray V, Kemp M, Klute W, Malet Sanz L, Miller D, Murata Y, Payne CE, Skerratt S, Stevens EB, Warmus JS.
Brown AD, et al. Among authors: fengas d.
Bioorg Med Chem. 2019 Jan 1;27(1):230-239. doi: 10.1016/j.bmc.2018.12.002. Epub 2018 Dec 4.
Bioorg Med Chem. 2019.
PMID: 30538065
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Identification of substance P metabolites using a combination of reversed-phase high-performance liquid chromatography and capillary electrophoresis.
Whelpton R, Michael-Titus AT, Stephens SM, Yau KW, Fengas D.
Whelpton R, et al. Among authors: fengas d.
J Chromatogr B Biomed Sci Appl. 1998 Sep 25;716(1-2):95-106. doi: 10.1016/s0378-4347(98)00334-x.
J Chromatogr B Biomed Sci Appl. 1998.
PMID: 9824222
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