DSP-2230
DSP-2230 is a selective small-molecule Nav1.7 and Nav1.8 voltage-gated sodium channel blocker which is under development by Dainippon Sumitomo Pharma for the treatment of neuropathic pain.[1][2] As of June 2014, it is in phase I/phase II clinical trials.[1][2]
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Routes of administration | By mouth |
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Formula | C20H20F3N5O2 |
Molar mass | 419.408 g·mol−1 |
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See also
References
- Martz, Lauren (2014). "Nav-i-gating antibodies for pain". Science-Business eXchange. 7 (23): 662. doi:10.1038/scibx.2014.662. ISSN 1945-3477.
- Bagal, Sharan K.; Chapman, Mark L.; Marron, Brian E.; Prime, Rebecca; Ian Storer, R.; Swain, Nigel A. (2014). "Recent progress in sodium channel modulators for pain". Bioorganic & Medicinal Chemistry Letters. 24 (16): 3690–9. doi:10.1016/j.bmcl.2014.06.038. ISSN 0960-894X. PMID 25060923.
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