EsCitalopram N-Desmethyl (Free Base)
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Documentation

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Includes: HPLC, MASS/LC-MS, 1H NMR, FT-IR, Potency, Structure Elucidation Report (SER), and additional analytical data depending on the product.

EsCitalopram N-Desmethyl (Free Base)

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Catalogue No.:VE006634
CAS No.:N/A
Mol. Formula:C19H19FN2O
Mol. Weight:310.4 g/mol

Additional information on EsCitalopram N-Desmethyl (Free Base)

Parent drug

Escitalopram

IUPAC Name

(S)-1-(4′-Fluorophenyl)-1-(3-(methylamino)propyl)-1, 3-dihydroisobenzo furan-5-carbonitrile

Synonyms

N/A

Description

It is one of impurity present in EsCitalopram, Escitalopram is a selective serotonin reuptake inhibitor, which enhances serotonergic activity by binding to the orthosteric binding site on the serotonin transporter, the same site to which endogenous 5-HT binds and thus prevents the reuptake of serotonin into the presynaptic neuron. It binds to a secondary allosteric site on the SERT molecule to inhibit 5-HT reuptake more. sustained elevation of synaptic 5HT eventually causes desensitization of 5-HT1A auto-receptors, which normally endogenous 5-HT release in the presence of excess 5-HT, this desensitization is needed for the clinical effect of SSRIs and is responsible for their typically prolonged onset of action

References

Landy, K., Rosani, A., & Estevez, R. (2022, October 9). Escitalopram. Retrieved November 4, 2022, from Nih.gov website: https://www.ncbi.nlm.nih.gov/books/NBK557734/

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