Clovoxamine

From Wikipedia, the free encyclopedia

Other namesDU-23811
ATC code
  • none
Legal status
  • In general: uncontrolled
Clovoxamine
Clinical data
Other namesDU-23811
Routes of
administration
Oral
ATC code
  • none
Legal status
Legal status
  • In general: uncontrolled
Identifiers
  • (E)-1-(4-chlorophenyl)-5-methoxy-1-pentanone O-(2-aminoethyl)oxime
CAS Number
PubChem CID
ChemSpider
UNII
ChEMBL
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC14H21ClN2O2
Molar mass284.78 g·mol−1
3D model (JSmol)
  • COCCCCC(=NOCCN)C1=CC=C(C=C1)Cl
  • InChI=1S/C14H21ClN2O2/c1-18-10-3-2-4-14(17-19-11-9-16)12-5-7-13(15)8-6-12/h5-8H,2-4,9-11,16H2,1H3/b17-14+ ☒N
  • Key:XXPVSQRPGBUFKM-SAPNQHFASA-N ☒N
 ☒NcheckY (what is this?)  (verify)

Clovoxamine (INN; development code DU-23811) is a drug that was discovered in the 1970s and was subsequently investigated as an antidepressant and anxiolytic agent but was never marketed.[1][2][3] It acts as a serotonin-norepinephrine reuptake inhibitor (SNRI), with little affinity for the muscarinic acetylcholine, histamine, adrenergic, and serotonin receptors.[4][5] The compound is structurally related to fluvoxamine.

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