Lubazodone
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File:Lubazodone structure.png | |
Systematic (IUPAC) name | |
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(2S)-2-[(7-fluoro-2,3-dihydro-1H-inden-4-yl)oxymethyl]morpholine | |
Clinical data | |
Routes of administration | Oral |
Legal status | |
Legal status |
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Identifiers | |
CAS Number | 161178-07-0 |
ATC code | none |
PubChem | CID 157919 |
Chemical data | |
Formula | C14H18FNO2 |
Molar mass | 251.296 g/mol[[Script error: No such module "String".]] |
Script error: No such module "collapsible list". | |
Lubazodone (YM-992, YM-35,995) is an antidepressant which was being developed as a treatment for depression but was discontinued. It acts as a serotonin reuptake inhibitor and 5-HT2A receptor antagonist. Lubazodone made it to phase II clinical trials but was discontinued in 2001.
See also
References
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This article does not cite any references or sources. Please help improve this article by adding citations to reliable sources. Unsourced material may be challenged and removed. (September 2009) |
GABAA PAMs |
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α2δ VDCC Blockers | |||||||||||
5-HT1A Agonists | |||||||||||
H1 Antagonists | Diphenylmethanes: Captodiame • Hydroxyzine; Others: Brompheniramine • Chlorpheniramine • Pheniramine | ||||||||||
CRH1 Antagonists | |||||||||||
NK2 Antagonists | |||||||||||
MCH1 antagonists | |||||||||||
mGluR2/3 Agonists | |||||||||||
mGluR5 NAMs | |||||||||||
TSPO agonists | |||||||||||
σ1 agonists | |||||||||||
Others | Benzoctamine • Carbetocin • Demoxytocin • Mephenoxalone • Mepiprazole • Oxanamide • Oxytocin • Promoxolane • Tofisopam • Trimetozine • WAY-267,464 | ||||||||||
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