Escitalopram (oxalate)


CAS No. : 219861-08-2

(Synonyms: (S)-Citalopram (oxalate); (S)-(+)-Citalopram (oxalate))

219861-08-2
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Cat. No. : HY-14258A
M.Wt: 414.43
Formula: C22H23FN2O5
Purity: >98 %
Solubility: H2O : ≥ 14.29 mg/mL;DMSO : 116.67 mg/mL (ultrasonic)
Introduction of 219861-08-2 :

Escitalopram ((S)-Citalopram) oxalate, the S-enantiomer of racemic Citalopram, is a selective serotonin reuptake inhibitor (SSRI) with a Ki of 0.89 nM. Escitalopram oxalate has ∼30 fold higher binding affinity than its R(-)-enantiomer and shows selectivity over both dopamine transporter (DAT) and norepinephrine transporter (NET). Escitalopram oxalate is an antidepressant for the research of major depression[1][2]. IC50 & Target: Ki: 0.89 nM (serotonin transporter), 10500 nM (DAT), 8150 nM (NET)[1] In Vivo: Escitalopram (10 mg/kg; i.p.; daily for 28 days) ameliorates cognitive impairments and selectively attenuates phosphorylated tau accumulation in stressed rats[3].
Chronic administration of Escitalopram (daily; drinking water for a total of 4 months) significantly reduces plaque load by 28% and 34% at 2.5 and 5 mg/d, respectively [4].

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