refers to the S(+)-ketamine, also known as esketamine, which is the purified dextrorotatory enantiomer of ketamine. It is recognized for its enhanced potency and improved safety profile compared to racemic ketamine (which contains both S- and R-enantiomers).
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S-Ketamine is the more active enantiomer of ketamine, exhibiting approximately four times stronger binding affinity to NMDA receptors than the R-enantiomer.
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It is FDA-approved in the form of Spravato nasal spray for treatment-resistant depression (TRD) and is used clinically for anesthesia and analgesia.
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S-Ketamine acts primarily as a non-competitive NMDA receptor antagonist, leading to dissociative anesthesia, analgesia, and rapid antidepressant effects.
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It also interacts with opioid, monoamine, adenosine, and other receptors, contributing to its broad pharmacological profile.
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: Higher NMDA receptor binding leads to stronger anesthetic and antidepressant effects at lower doses.
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Anesthesia and sedation, especially in emergency and intensive care settings.
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Rapid relief of treatment-resistant depression and suicidal ideation via intranasal administration.
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Analgesia and neuroprotection in various clinical scenarios.
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Dissociation, hallucinations, dizziness, nausea, increased salivation, and increased heart rate and blood pressure.
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Generally fewer psychotropic side effects compared to racemic ketamine.
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: Stimulates sympathetic nervous system, causing temporary increases in heart rate and blood pressure, with minimal respiratory depression at therapeutic doses.
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More potent and effective at lower doses.
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Reduced incidence of psychotropic adverse effects like hallucinations and dissociation.
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Faster onset and more sustained antidepressant effects.
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Approved for clinical use in specific formulations (e.g., Spravato nasal spray).
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Pure S-ketamine is typically available as a clear, colorless liquid for injection or as a nasal spray formulation.
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The “Type-S” designation highlights its enantiomeric purity and clinical-grade quality.
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