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  2. Sodium thiopental - Wikipedia

    en.wikipedia.org/wiki/Sodium_thiopental

    Sodium thiopental is an ultra-short-acting barbiturate and has been used commonly in the induction phase of general anesthesia.Its use has been largely replaced with that of propofol, but may retain some popularity as an induction agent for rapid-sequence induction and intubation, such as in obstetrics. [12]

  3. Barbiturate - Wikipedia

    en.wikipedia.org/wiki/Barbiturate

    Thiopental is a barbiturate with one of the C=O double bonds (with the carbon being labelled 2 in the adjacent diagram) replaced with a C=S double bond, R 1 being CH 2 CH 3 (ethyl) and R3) being CH(CH 3)CH 2 CH 2 CH 3 (sec-pentyl). Thiopental is no longer available in the United States. [47]

  4. Truth serum - Wikipedia

    en.wikipedia.org/wiki/Truth_serum

    Amobarbital, one of the chemical compounds that can be used as a truth serum. Sedatives or hypnotics that alter higher cognitive function include ethanol, scopolamine, 3-quinuclidinyl benzilate, potent short or intermediate acting hypnotic benzodiazepines such as midazolam, flunitrazepam, and various short and ultra-short acting barbiturates, including sodium thiopental (commonly known by the ...

  5. Hexobarbital - Wikipedia

    en.wikipedia.org/wiki/Hexobarbital

    Hexobarbital or hexobarbitone, sold both in acid and sodium salt forms as Citopan, Evipan, and Tobinal, is a barbiturate derivative having hypnotic and sedative effects. It was used in the 1940s and 1950s as an agent for inducing anesthesia for surgery, as well as a rapid-acting, short-lasting hypnotic for general use, and has a relatively fast onset of effects and short duration of action. [1]

  6. Methohexital - Wikipedia

    en.wikipedia.org/wiki/Methohexital

    This increases the length of time which the Cl − ionopores are open, thus causing an inhibitory effect. Metabolism of methohexital is primarily hepatic via demethylation and oxidation. [ 1 ] Side-chain oxidation is the primary means of metabolism involved in the termination of the drug's biological activity .

  7. Context-sensitive half-life - Wikipedia

    en.wikipedia.org/wiki/Context-sensitive_half-life

    Context-sensitive half-life or context sensitive half-time is defined as the time taken for blood plasma concentration of a drug to decline by one half after an infusion designed to maintain a steady state (i.e. a constant plasma concentration) has been stopped. The "context" is the duration of infusion.

  8. Pharmacodynamics - Wikipedia

    en.wikipedia.org/wiki/Pharmacodynamics

    The duration of action of a drug is the length of time that particular drug is effective. [5] Duration of action is a function of several parameters including plasma half-life, the time to equilibrate between plasma and target compartments, and the off rate of the drug from its biological target. [6]

  9. Onset of action - Wikipedia

    en.wikipedia.org/wiki/Onset_of_action

    Onset of action is the duration of time it takes for a drug's effects to come to prominence upon administration. With oral administration , it typically ranges anywhere from 20 minutes to over an hour, depending on the drug in question.