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  1. Jul 31, 2007 · Indication Contraindications & Blackbox Warnings Pharmacodynamics Mechanism of action Absorption Volume of distribution Protein binding Metabolism Route of elimination Half-life Clearance Adverse Effects Toxicity Pathways Pharmacogenomic Effects/ADRs

  2. Jan 1, 2016 · The underlying mechanism of the emergence phenomena caused by arylcyclohexamines appears to be due to their depressive effects on visual and auditory relay nuclei in the medial geniculate and inferior colliculus, respectively, leading to misperception and/or misinterpretation of visual and auditory stimuli [287, 288].

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  4. Jan 30, 2022 · PCP is a noncompetitive antagonist at the glutamate NMDA receptor and binds to sites located in the cortex and limbic structures of the brain. This mechanism is believed to be responsible for most of the dissociative effects of PCP.

  5. Jan 30, 2024 · Mechanism of Action. Ketamine hydrochloride is a nonbarbiturate dissociative anesthetic. As a cyclohexanone derivative, the drug rapidly acts and produces profound anesthesia and analgesia. Its chemical name is ±)-2-(o-chlorophenyl)-2-(methylamino) cyclohexanone hydrochloride; the structural formula is CHClNO.

    • 2024/01/30
    • Learning Objective. Describe the mechanisms of action associated with drugs that inhibit cell wall biosynthesis, protein synthesis, membrane function, nucleic acid synthesis, and metabolic pathways.
    • Inhibitors of Cell Wall Biosynthesis. Several different classes of antibacterials block steps in the biosynthesis of peptidoglycan, making cells more susceptible to osmotic lysis (Table 14.2).
    • Inhibitors of Protein Biosynthesis. The cytoplasmic ribosomes found in animal cells (80S) are structurally distinct from those found in bacterial cells (70S), making protein biosynthesis a good selective target for antibacterial drugs.
    • Inhibitors of Membrane Function. A small group of antibacterials target the bacterial membrane as their mode of action (Table 14.4). The polymyxins are natural polypeptide antibiotics that were first discovered in 1947 as products of Bacillus polymyxa; only polymyxin B and polymyxin E (colistin) have been used clinically.
  6. Feb 6, 2010 · IUPAC Standard InChI: InChI=1S/C12H17N/c1-3-7-11(8-4-1)13-12-9-5-2-6-10-12/h1,3-4,7-8,12-13H,2,5-6,9-10H2 Copy IUPAC Standard InChIKey: TXTHKGMZDDTZFD-UHFFFAOYSA-N ...

  7. Toxicokinetics. Phencyclidine, or 1- (1-phenylcyclohexyl) piperidine, is synthesized from piperidine and cyclohexanone. It is a highly lipid-soluble solid that is soluble in both water and alcohol. It is a weak base with a pKa between 8.6 and 9.4. The dose of PCP varies depending on the amount of active drug and the route.

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