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  2. Esketamine - Wikipedia

    en.wikipedia.org/wiki/Esketamine

    Esketamine is eliminated from the human body more quickly than arketamine (R(–)-ketamine) or racemic ketamine, although arketamine slows the elimination of esketamine. [62] The half-life of esketamine was found to be approximately 5 hours. [63] When administered intranasally, esketamine’s bioavailability is approximately 30–50%. [63]

  3. Ketamine - Wikipedia

    en.wikipedia.org/wiki/Ketamine

    Elimination half-life: Ketamine: 2.5–3 hours [13] [7] Norketamine: 12 hours [14] ... Esketamine is a far more potent NMDA receptor pore blocker than arketamine. [11]

  4. Ketamine in society and culture - Wikipedia

    en.wikipedia.org/wiki/Ketamine_in_society_and...

    After the publication of the NIH-run antidepressant clinical trial, clinics began opening in which the intravenous ketamine is given for depression. [5] [6] This practice is an off label use of IV ketamine in the United States, though the intranasal version of esketamine has been approved by the FDA for treatment of depression [5] [7] In 2015 there were about 60 such clinics in the US; the ...

  5. Arketamine - Wikipedia

    en.wikipedia.org/wiki/Arketamine

    Arketamine (developmental code names PCN-101, HR-071603), also known as (R)-ketamine or (R)-(−)-ketamine, is the (R)-(−) enantiomer of ketamine. [1] [2] [3] Similarly to racemic ketamine and esketamine, the S(+) enantiomer of ketamine, arketamine is biologically active; however, it is less potent as an NMDA receptor antagonist and anesthetic and thus has never been approved or marketed for ...

  6. Norketamine - Wikipedia

    en.wikipedia.org/wiki/Norketamine

    Unlike esketamine, (S)-norketamine does not appear to significantly impact prepulse inhibition (reduction of the startle reflex) and as such appears to have significantly fewer psychotomimetic effects - which may indicate that it could be a safer alternative to ketamine for use as an antidepressant in humans.

  7. 25-NB - Wikipedia

    en.wikipedia.org/wiki/25-NB

    General structure of 25-NB derivatives, where R is usually 2,5-dimethoxy-4-(alkyl or halogen), R 1 is usually H but rarely methyl, and Cyc is usually 2-substituted phenyl but can be other heterocycles.

  8. Oxiracetam - Wikipedia

    en.wikipedia.org/wiki/Oxiracetam

    The half-life of oxiracetam in healthy individuals is about 8 hours, whereas it is 10–68 hours in patients with renal impairment. There is some penetration of the blood–brain barrier with brain concentrations reaching 5.3% of those in the blood (measured one hour after a single 2000 mg intravenous dose).

  9. N-Ethylnorketamine - Wikipedia

    en.wikipedia.org/wiki/N-Ethylnorketamine

    N-Ethylnorketamine (ethketamine, NENK, 2-Cl-2'-Oxo-PCE) is a designer drug which is presumed to have similar properties to ketamine, a dissociative anesthetic drug with hallucinogenic and sedative effects.