Chemistry:DSP-2230
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Short description: Investigational analgesic drug
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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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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]
See also
References
- ↑ 1.0 1.1 Martz, Lauren (2014). "Nav-i-gating antibodies for pain". Science-Business EXchange 7 (23): 662. doi:10.1038/scibx.2014.662. ISSN 1945-3477.
- ↑ 2.0 2.1 "Recent progress in sodium channel modulators for pain". Bioorganic & Medicinal Chemistry Letters 24 (16): 3690–9. August 2014. doi:10.1016/j.bmcl.2014.06.038. PMID 25060923.
External links
- "DSP-2230". AdisInsight. Springer Nature Switzerland AG. http://adisinsight.springer.com/drugs/800036041.
Original source: https://en.wikipedia.org/wiki/DSP-2230.
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