Citalopram Hydrobromide Salt is a selective inhibitor of the ST (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 behaviour.
API's & Drug Standards
|Formula||C19D3H16FN2O · HCl|
|Storage Conditions||Room temperature|
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