Esketamine

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(Redirected from Spravato)

File:Short-term antidepressant efficacy of esketamine versus placebo added to an existing oral antidepressant in people with depression.png
Short-term_antidepressant_efficacy_of_esketamine_versus_placebo_added_to_an_existing_oral_antidepressant_in_people_with_depression.png
File:Short-term antidepressant efficacy of esketamine versus placebo added to an existing oral antidepressant in people with depression and suicidality.png
Short-term_antidepressant_efficacy_of_esketamine_versus_placebo_added_to_an_existing_oral_antidepressant_in_people_with_depression_and_suicidality.png

Medication used for treatment-resistant depression

Esketamine

Esketamine

Esketamine

Trade names Spravato


Chemical nomenclature
IUPAC name (2S)-2-(2-chlorophenyl)-2-(methylamino)cyclohexanone



Routes Nasal spray



Metabolism Liver (CYP2B6, CYP3A4)
Half-life 7-12 hours
Excretion Urine


Identifiers
CAS Number 33643-46-8
PubChem 123631
DrugBank DB01221
ChemSpider 110146
UNII 50LFG48P1T
KEGG D09373
ChEMBL 1201208
Chemical data


Chemical formula C13H16N1O1Cl1


SMILES ClC1=CC=CC=C1[C@@H](C2(NC)CCCCC2)=O
InChI 1S/C13H16ClNO/c1-15-12(13(16)10-6-2-3-7-10)9-4-5-8-11(14)12/h4-5,8-10,15H,2-3,6-7H2,1H3/t12-/m0/s1
InChIKey YQEZLKZALYSWHR-LBPRGKRZSA-N


Esketamine, sold under the brand name Spravato, is a medication used for the treatment of treatment-resistant depression (TRD). It is a stereoisomer of ketamine, specifically the S(+) enantiomer. Esketamine is administered as a nasal spray and works as a NMDA receptor antagonist.

Medical uses[edit]

Esketamine is primarily used for treatment-resistant depression in adults who have not responded adequately to at least two different antidepressant treatments. It is often used in conjunction with an oral antidepressant.

Mechanism of action[edit]

Esketamine acts as a NMDA receptor antagonist, which is believed to contribute to its rapid antidepressant effects. By blocking the NMDA receptor, esketamine increases the levels of glutamate in the brain, which in turn activates AMPA receptors and leads to the release of brain-derived neurotrophic factor (BDNF). This cascade of events is thought to contribute to the synaptic plasticity and antidepressant effects observed with esketamine.

Side effects[edit]

Common side effects of esketamine include dissociation, dizziness, nausea, sedation, vertigo, and increased blood pressure. Due to its potential for abuse and dissociative effects, esketamine is classified as a Schedule III controlled substance in the United States.

History[edit]

Esketamine was approved by the U.S. Food and Drug Administration (FDA) in March 2019 for the treatment of treatment-resistant depression. It was developed by Janssen Pharmaceuticals, a subsidiary of Johnson & Johnson.

Related pages[edit]

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