Date published: 2026-4-24

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(S)-Citalopram Fluorophenylmethanone Oxalate Impurity

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Application:
Molecular Weight:
511.51
Molecular Formula:
C28H27F2NO6
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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(S)-Citalopram Fluorophenylmethanone Oxalate Impurity is an impurity of Citalopram (sc-201123). Citalopram is a selective inhibitor of the 5-hydroxytryptamine transporter (serotonin) and therefore is a potent and selective serotonin reuptake inhibitor. Additional studies in indicate that Citalopram may be a weak, allosteric modulator of serotonin in a cross-species chimeric study. Studies also indicate that Citalopram is useful for studying gene expression patterns in circulating lymphocytes. In zebrafish, Citalopram is noted to reduce the frequency of NMDA-induced locomotor rhythm involved in swimming behavor.


(S)-Citalopram Fluorophenylmethanone Oxalate Impurity References

  1. Plasma membrane monoamine transporters: structure, regulation and function.  |  Torres, GE., et al. 2003. Nat Rev Neurosci. 4: 13-25. PMID: 12511858
  2. The effect of citalopram on gene expression profile of Alzheimer lymphocytes.  |  Palotás, A., et al. 2004. Neurochem Res. 29: 1563-70. PMID: 15260135
  3. Dissection of an allosteric mechanism on the serotonin transporter: a cross-species study.  |  Neubauer, HA., et al. 2006. Mol Pharmacol. 69: 1242-50. PMID: 16434615
  4. Serotonergic modulation of locomotion in zebrafish: endogenous release and synaptic mechanisms.  |  Gabriel, JP., et al. 2009. J Neurosci. 29: 10387-95. PMID: 19692613

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

(S)-Citalopram Fluorophenylmethanone Oxalate Impurity, 10 mg

sc-220065
10 mg
$360.00