59729-32-7

Citalopram hydrobromide (XU-62-320) , a selective serotonin reuptake inhibitor (SSRI), selectively inhibits the CNS neuronal reuptake of serotonin, thereby potentiating serotonergic activity in the central nervous system (CNS). Citalopram hydrobromide is the orally bioavailable hydrobromide salt of the racemic bicyclic phthalene derivative citalopram with antidepressant activity. This agent has minimal effects on the CNS neuronal reuptake of norepinephrine (NE) and dopamine (DA).

Citalopram (Standard) is a reference standard for research and analysis in studies involving Citalopram. Citalopram (Lu 10-171 is an orally active, selective serotonin reuptake inhibitor (SSRI), a selective 5-hydroxytryptamine reuptake inhibitor, and a racemic mixture of the S(+)-enantiomer (Escitalopram) and the R(-)-enantiomer.Citalopram exhibits antidepressant activity and enhances serotonergic neurotransmission. It can be used to study Alzheimer's disease.

Citalopram-D4 hydrobromide is the deuterated form of Citalopram hydrobromide (T1483), which is a selective serotonin reuptake inhibitor (SSRI).

(R)-Citalopram oxalate is a weak selective serotonin reuptake inhibitor (SSRI) that antagonises its S-isomer (escitalopram), slightly reducing its inhibition of the serotonin transporter, and exhibits anticonvulsant and antidepressant effects.

Citalopram-D4 Oxalate is a deuterated compound of Citalopram Oxalate. Citalopram Oxalate has a CAS number of 207559-01-1.

Citalopram-D6 Oxalate is a deuterated compound of Citalopram Oxalate. Citalopram Oxalate (T69943) has a CAS number of 207559-01-1.

Citalopram-D6 is a deuterated compound of Citalopram. Citalopram (T20828) has a CAS number of 59729-33-8. Citalopram (T20828) (Lu 10-171 is an orally active, selective serotonin reuptake inhibitor (SSRI), a selective 5-hydroxytryptamine reuptake inhibitor, and a racemic mixture of the S (+)-enantiomer (Escitalopram) and the R (-)-enantiomer.Citalopram exhibits antidepressant activity and enhances serotonergic neurotransmission. It can be used to study Alzheimer's disease.

Citalopram-D4 Hydrobromide (Standard) is a reference standard of Citalopram-D4 Hydrobromide intended for quantitative analysis, quality control, and related biochemical research applications. Citalopram-d4 (hydrobromide) is the deuterated form of Citalopram hydrobromide, which is a selective serotonin reuptake inhibitor (SSRI).

Citalopram-[D4] Oxalate (Standard) is a reference standard of Citalopram-[D4] Oxalate intended for quantitative analysis, quality control, and related biochemical research applications.

Citalopram oxalate is a furancarbonitrile that is one of the SEROTONIN UPTAKE INHIBITORS used as an antidepressant. The drug is also effective in reducing ethanol uptake in alcoholics and is used in depressed patients who also suffer from tardive dyskinesia in preference to tricyclic antidepressants, which aggravate this condition.

Escitalopram (Seroplex) is a furancarbonitrile that is one of the SEROTONIN UPTAKE INHIBITORS used as an antidepressant. The drug is also effective in reducing ethanol uptake in alcoholics and is used in depressed patients who also suffer from tardive dyskinesia in preference to tricyclic antidepressants, which aggravate this condition.

Citalopram (Lu 10-171 is an orally active, selective serotonin reuptake inhibitor (SSRI), a selective 5-hydroxytryptamine reuptake inhibitor, and a racemic mixture of the S(+)-enantiomer (Escitalopram) and the R(-)-enantiomer.Citalopram exhibits antidepressant activity and enhances serotonergic neurotransmission. It can be used to study Alzheimer's disease.

Fluvastatin sodium (Fluvastatin sodium salt), a competitive inhibitor of hydroxymethylglutaryl-coenzyme A reductase (HMGCR), is a commonly used cholesterol lowering agent.