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(+)-Femoxetine

HCID 3012003
NotesReactions
Basic informationOverviewNames & identifiersPropertiesChemistry & industryRelated reactionsCompound notes
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Basic information

CAS
59859-58-4
Standard SMILES
COc1ccc(OC[C@H]2CN(C)CC[C@@H]2c2ccccc2)cc1
InChIKey
OJSFTALXCYKKFQ-YLJYHZDGSA-N
Molecular formula
C20H25NO2
Average molar mass
311.4 g/mol
Monoisotopic mass
311.18852904

Overview

Femoxetine is a member of piperidines.

Names & identifiers

Preferred name
(+)-Femoxetine
IUPAC
(3R,4S)-3-[(4-methoxyphenoxy)methyl]-1-methyl-4-phenylpiperidine
English name
Femoxetine
Molecular formula
C20H25NO2
Molecular weight
311.42

Names & synonyms

Femoxetine59859-58-4Femoxetina(+)-FemoxetineFemoxetinum8Y719ZLX8CDTXSID70208576Piperidine, 3-((4-methoxyphenoxy)methyl)-1-methyl-4-phenyl-, (3R-trans)-femoxitineRefChem:140087DTXCID20131067trans-3-((4-methoxyphenoxy)methyl)-1-methyl-4-phenylpiperidine
Show more names
Malexil(3R)-1-Methyl-3α-(4-methoxyphenoxymethyl)-4β-phenylpiperidine(3R)-3α-[(4-Methoxyphenoxy)methyl]-1-methyl-4β-phenylpiperidinePiperidine, 3-[(4-methoxyphenoxy)methyl]-1-methyl-4-phenyl-, (3R,4S)-
trans-(+)-3-((4-methoxyphenoxy)methyl)-1-methyl-4-phenylpiperidineFemoxetine [INN](3R,4S)-3-[(4-methoxyphenoxy)methyl]-1-methyl-4-phenylpiperidineFemoxetinum [INN-Latin]Femoxetina [INN-Spanish]UNII-8Y719ZLX8CCHEMBL94739(+)-trans-3-((p-Methoxyphenoxy)methyl)-1-methyl-4-phenylpiperidine

Database identifiers

CAS
59859-58-4
PubChem CID
3012003
DTXSID

Properties

Computed structural properties

XLogP
4
Topological polar surface area
21.7 Ų
Hydrogen bond donors
0
Hydrogen bond acceptors
3
Rotatable bonds
5
Heavy atoms
23
Formal charge
0
Complexity
335

Physicochemical properties

Boiling point
437.9 · 437.9±35.0 °C(Predicted)
Density
1.055 · 1.055±0.06 g/cm3(Predicted)
pka
8 · 8+-.0.10(Predicted)
FDA UNII
8 Y719ZLX8C · 8Y719ZLX8C

Chemistry & industry

Pharmacology

MeSH Pharmacological Classification · 3 items

Substances that prevent infectious agents or organisms from spreading or kill infectious agents in order to prevent the spread of infection.

Mood-stimulating drugs used primarily in the treatment of affective disorders and related conditions. Several MONOAMINE OXIDASE INHIBITORS are useful as antidepressants apparently as a long-term consequence of their modulation of catecholamine levels. The tricyclic compounds useful as antidepressive agents (ANTIDEPRESSIVE AGENTS, TRICYCLIC) also appear to act through brain catecholamine systems. A third group (ANTIDEPRESSIVE AGENTS, SECOND-GENERATION) is a diverse group of drugs including some that act specifically on serotonergic systems.

Compounds that specifically inhibit the reuptake of serotonin in the brain.

Applications

Uses(+)-Femoxetine is an antidepressant drug.

Suppliers6 total

LGM Pharma1-(800)-881-8210 · [email protected]
北京博奥森生物技术有限公司400-901-9800 18611424007 · [email protected]
上海陶术生物科技股份有限公司+1-781-999-5354; +1-00000000000 · [email protected]
上海一飞生物科技有限公司021-65675885 18964387627 · [email protected]
TargetMol中国(陶术生物)15002134094 · [email protected]
上海阿摩尔生物科技有限公司13370042665 18916960931 · [email protected]

Additional notes

Related reactions

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Compound notes

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On this pageBasic informationOverviewNames & identifiersPropertiesChemistry & industryRelated reactionsCompound notes
DTXSID70208576
ChEMBL
CHEMBL94739
ChEBI
CHEBI:135330
UNII
8Y719ZLX8C
Nikkaji
J18.188I

DefinitionChEBI: Femoxetine is a member of piperidines.