From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
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Clinical data | |
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Other names | (–)-1-(1-dimethylaminomethyl) 5-methoxybenzocyclobutan-1-yl) cyclohexanol |
Identifiers | |
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CAS Number | |
PubChem CID | |
ChemSpider | |
UNII | |
CompTox Dashboard (EPA) | |
Chemical and physical data | |
Formula | C18H27NO2 |
Molar mass | 289.419 g·mol−1 |
3D model (JSmol) | |
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S33005 is a serotonin–norepinephrine reuptake inhibitor (SNRI) that was under development by Servier for the treatment of depression and related disorders. It is structurally related to venlafaxine but has a more complex molecular structure. Venlafaxine appears to be a sigma modulator,[1] but it is not known if S33005 shares this activity.
Synthesis
[edit]"The 1-cyano-benzocyclobutenes used as starting material are obtained, for example, by subjecting a β-[orthohalogeno-phenyl]-propionitrile to intramolecular condensation in the presence of potassium amide, or by brominating a benzocyclobutene in position 1 with N-bromosuccinimide, followed by exchange of the bromine atom for a cyano group by means of sodium cyanide."[2]
See also
[edit]References
[edit]- ^ Dhir A, Kulkarni SK (June 2007). "Involvement of sigma-1 receptor modulation in the antidepressant action of venlafaxine". Neuroscience Letters. 420 (3): 204–8. doi:10.1016/j.neulet.2007.04.055. PMID 17532136. S2CID 25971336.
- ^ U.S. patent 3,622,614
External links
[edit]- PubMed search
- Binding Database
- The patent and synthesis discussion can be found in U.S. patent 6,107,345
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Retrieved from "https://teknopedia.ac.id/w/index.php?title=S33005&oldid=1284704353"
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