Clovoxamine

Last updated
Clovoxamine
Clovoxamine Structure.svg
Clinical data
Routes of
administration
Oral
ATC code
  • none
Legal status
Legal status
  • In general: uncontrolled
Identifiers
  • 1-(4-chlorophenyl)-5-methoxypentan-1-one O-2-aminoethyl oxime
CAS Number
PubChem CID
ChemSpider
UNII
ChEMBL
CompTox Dashboard (EPA)
Chemical and physical data
Formula C14H21ClN2O2
Molar mass 284.78 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+ X mark.svgN
  • Key:XXPVSQRPGBUFKM-SAPNQHFASA-N X mark.svgN
 X mark.svgNYes check.svgY  (what is this?)    (verify)

Clovoxamine (INN) (developmental code name 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.

Related Research Articles

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<span class="mw-page-title-main">Serotonin–norepinephrine reuptake inhibitor</span> Class of antidepressant medication

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<span class="mw-page-title-main">Clomipramine</span> Antidepressant

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<span class="mw-page-title-main">Serotonin reuptake inhibitor</span> Class of drug

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<span class="mw-page-title-main">Tandamine</span> Chemical compound

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<span class="mw-page-title-main">Levomilnacipran</span> SNRI antidepressant drug

Levomilnacipran is an antidepressant which was approved in the United States in 2013 for the treatment of major depressive disorder (MDD) in adults. It is the levorotatory enantiomer of milnacipran, and has similar effects and pharmacology, acting as a serotonin–norepinephrine reuptake inhibitor (SNRI).

<span class="mw-page-title-main">Selective serotonin reuptake inhibitor</span> Class of antidepressant medication

Selective serotonin reuptake inhibitors (SSRIs) are a class of drugs that are typically used as antidepressants in the treatment of major depressive disorder, anxiety disorders, and other psychological conditions.

<span class="mw-page-title-main">Pridefine</span> Chemical compound

Pridefine (AHR-1,118) is a drug which was investigated as an antidepressant in the late 1970s and early 1980s, but was never marketed. It acts as a balanced reuptake inhibitor of serotonin, dopamine, and norepinephrine, and also has some weak releasing activity.

Selective serotonin reuptake inhibitors, or serotonin-specific re-uptake inhibitor (SSRIs), are a class of chemical compounds that have application as antidepressants and in the treatment of depression and other psychiatric disorders. SSRIs are therapeutically useful in the treatment of panic disorder (PD), posttraumatic stress disorder (PTSD), social anxiety disorder, obsessive-compulsive disorder (OCD), premenstrual dysphoric disorder (PMDD), and anorexia. There is also clinical evidence of the value of SSRIs in the treatment of the symptoms of schizophrenia and their ability to prevent cardiovascular diseases.

References

  1. Freeman HL, Wakelin JS, Calanca A, Hole G (1982). "Initial clinical evaluation of a new nontricyclic antidepressant: clovoxamine". Advances in Biochemical Psychopharmacology. 32: 69–75. PMID   7046368.
  2. Jesinger DK, Gostick N (October 1989). "Anxiety neurosis in general practice. A double-blind comparative study of diazepam and clovoxamine, a novel inhibitor of noradrenaline and serotonin reuptake". International Clinical Psychopharmacology. 4 (4): 301–11. doi:10.1097/00004850-198910000-00005. PMID   2691573.
  3. Hurst HE, Jones DR, Wright JH, Jarboe CH (August 1983). "Clovoxamine kinetics in an early clinical trial". Clinical Pharmacology and Therapeutics. 34 (2): 266–71. doi:10.1038/clpt.1983.164. PMID   6872422. S2CID   42205772.
  4. Saletu B, Grünberger J, Rajna P, Karobath M (1980). "Clovoxamine and fluvoxamine-2 biogenic amine re-uptake inhibiting antidepressants: quantitative EEG, psychometric and pharmacokinetic studies in man". Journal of Neural Transmission. 49 (1–2): 63–86. doi:10.1007/BF01249190. PMID   6777458. S2CID   6483654.
  5. Bradford LD, Tulp MT, Schipper J (June 1987). "Biochemical effects in rats after acute and long-term treatment with clovoxamine". Archives Internationales de Pharmacodynamie et de Therapie. 287 (2): 188–202. PMID   2820327.