Esreboxetine
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File:Esreboxetine.png | |
Systematic (IUPAC) name | |
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(2S)-2-[(S)-(2-ethoxyphenoxy)phenylmethyl]morpholine | |
Clinical data | |
Routes of administration | Oral |
Legal status | |
Legal status |
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Identifiers | |
CAS Number | 98819-76-2 |
ATC code | none |
Chemical data | |
Formula | C19H23NO3 |
Molar mass | 313.391 g/mol[[Script error: No such module "String".]] |
Esreboxetine is a selective norepinephrine reuptake inhibitor which was under development by Pfizer for the treatment of neuropathic pain and fibromyalgia but failed to show significant benefit over currently available medications and was discontinued.[1][2][3][4] It is the (+)-(S,S)-enantiomer of reboxetine and is even more selective in comparison.[1][5]
See also
References
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40px | This analgesic-related article is a stub. You can help ssf by expanding it. |
- ↑ 1.0 1.1 Matilda Bingham; Napier, Susan Jolliffe (2009). Transporters as Targets for Drugs (Topics in Medicinal Chemistry). Berlin: Springer. ISBN 3-540-87911-0. CS1 maint: Multiple names: authors list (link)
- ↑ Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
- ↑ "Search of: esreboxetine - List Results - ClinicalTrials.gov".
- ↑ "Musculoskeletal Report: Pfizer Stops Work on Esreboxetine for FM".
- ↑ Fish, P. V.; MacKenny, M.; Bish, G.; Buxton, T.; Cave, R.; Drouard, D.; Hoople, D.; Jessiman, A.; Miller, D. (2009). "Enantioselective synthesis of (R)- and (S)-N-Boc-morpholine-2-carboxylic acids by enzyme-catalyzed kinetic resolution: application to the synthesis of reboxetine analogs". Tetrahedron Letters. 50: 389. doi:10.1016/j.tetlet.2008.11.025. edit
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