Femoxetine
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File:Femoxetine.png | |
Systematic (IUPAC) name | |
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(3R,4S)-3-[(4-methoxyphenoxy)methyl]-1-methyl-4-phenyl-piperidine | |
Clinical data | |
Routes of administration | Oral |
Legal status | |
Legal status |
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Pharmacokinetic data | |
Biological half-life | 7-27 hours |
Identifiers | |
CAS Number | 59859-58-4 |
ATC code | none |
PubChem | CID 3012003 |
ChemSpider | 2280941 |
Chemical data | |
Formula | C20H25NO2 |
Molar mass | 311.42 g/mol[[Script error: No such module "String".]] |
Script error: No such module "collapsible list". | |
Femoxetine (Malexil, FG-4963) is a drug related to paroxetine that was being developed as an antidepressant by the pharmaceutical company Ferrosan in 1974. It functions as a selective serotonin reuptake inhibitor (SSRI). Development was halted for unknown reasons, perhaps to focus attention on paroxetine instead.
Dr. Jorgen Buus-Lassen of Ferrosan invented both femoxetine and paroxetine in the 1970s.[1]
References
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This article needs additional citations for verification. Please help improve this article by adding citations to reliable sources. Unsourced material may be challenged and removed. (June 2009) |
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α2δ VDCC Blockers | |||||||||||
5-HT1A Agonists | |||||||||||
H1 Antagonists | Diphenylmethanes: Captodiame • Hydroxyzine; Others: Brompheniramine • Chlorpheniramine • Pheniramine | ||||||||||
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σ1 agonists | |||||||||||
Others | Benzoctamine • Carbetocin • Demoxytocin • Mephenoxalone • Mepiprazole • Oxanamide • Oxytocin • Promoxolane • Tofisopam • Trimetozine • WAY-267,464 | ||||||||||
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