Brofaromine

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Brofaromine
Brofaromine.svg
Systematic (IUPAC) name
4-(7-bromo-5-methoxybenzofuran-2-yl)piperidine
Clinical data
Legal status
  • ℞ (Prescription only)
Routes of
administration
Oral
Pharmacokinetic data
Protein binding 98%
Biological half-life 9-14 hours
Identifiers
CAS Number 63638-91-5 YesY
ATC code none
PubChem CID: 44571
ChemSpider 40549 YesY
UNII 6WV4B8Q07H YesY
KEGG D02560 YesY
ChEMBL CHEMBL160347 YesY
Chemical data
Formula C14H16BrNO2
Molecular mass 310.186 g/mol
  • Brc3cc(OC)cc1c3oc(c1)C2CCNCC2
  • InChI=1S/C14H16BrNO2/c1-17-11-6-10-7-13(9-2-4-16-5-3-9)18-14(10)12(15)8-11/h6-9,16H,2-5H2,1H3 YesY
  • Key:WZXHSWVDAYOFPE-UHFFFAOYSA-N YesY
  (verify)

Brofaromine (proposed brand name Consonar) is a reversible inhibitor of monoamine oxidase A (RIMA) discovered by Ciba-Geigy.[1] The compound was primarily researched in the treatment of depression and anxiety but its development was dropped before it was brought to market.[2]

Brofaromine also acts as a serotonin reuptake inhibitor, and its dual pharmacologic effects offered promise in the treatment of a wide spectrum of depressed patients while producing less severe anticholinergic side effects in comparison with older standard drugs like the tricyclic antidepressants.

Pharmacology

Brofaromine is a reversible inhibitor of monoamine oxidase A (RIMA, a type of monoamine oxidase inhibitor (MAOI)) and acts on epinephrine (adrenaline), norepinephrine (noradrenaline), serotonin, and dopamine. Unlike standard MAOIs, possible side effects do not include cardiovascular complications (hypertension) with encephalopathy, liver toxicity or hyperthermia.

References

  1. US Patent 4210655
  2. Lua error in package.lua at line 80: module 'strict' not found. Free full text


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