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  2. Chen-Kao reaction - Wikipedia

    en.wikipedia.org/wiki/Chen-Kao_reaction

    Chelate complex of the Chen-Kao reaction starting from (1S,2S)-pseudoephedrine. The Chen-Kao reaction (named after Ko Kuei Chen and Chung-Hsi Kao, Madison, Wisconsin 1926) [1] [2] is a chemical method for determining the presence of pseudoephedrine, ephedrine, and similar phenylalkylamines. [3]

  3. Standard for the Uniform Scheduling of Medicines and Poisons

    en.wikipedia.org/wiki/Standard_for_the_Uniform...

    The SUSMP classifies drugs and poisons into different Schedules signifying the degree of control recommended to be exercised over their availability to the public. [3] The Schedules are referred to under State and Territory legislation for regulatory purposes. Although each State and Territory has its own laws, the vast majority of medicines ...

  4. Phenylpropanolamine - Wikipedia

    en.wikipedia.org/wiki/Phenylpropanolamine

    In June 2024, the US Food and Drug Administration (FDA) approved Phenylpropanolamine Hydrochloride chewable tablets for the control of urinary incontinence due to a weakening of the muscles that control urination (urethral sphincter hypotonus) in dogs. [78] [79] [80] This is the first generic phenylpropanolamine hydrochloride chewable tablets ...

  5. Pseudoephedrine - Wikipedia

    en.wikipedia.org/wiki/Pseudoephedrine

    Pseudoephedrine is excreted through urine, and the concentration in urine of this drug shows a large inter-individual spread; that is, the same dose can give a vast difference in urine concentration for different individuals. [123] Pseudoephedrine is approved to be taken up to 240 mg per day.

  6. Sympathomimetic drug - Wikipedia

    en.wikipedia.org/wiki/Sympathomimetic_drug

    The mechanisms of sympathomimetic drugs can be direct-acting (direct interaction between drug and receptor), such as α-adrenergic agonists, β-adrenergic agonists, and dopaminergic agonists; or indirect-acting (interaction not between drug and receptor), such as MAOIs, COMT inhibitors, release stimulants, and reuptake inhibitors that increase the levels of endogenous catecholamines.

  7. Ephedra (medicine) - Wikipedia

    en.wikipedia.org/wiki/Ephedra_(medicine)

    A wide variety of alkaloid and non-alkaloid compounds have been identified in various species of ephedra.Of the six ephedrine-type ingredients found in ephedra (at concentrations of 0.02-3.4%), the most common are ephedrine and pseudoephedrine, [12] which are the sources of its stimulant and thermogenic effects. [3]

  8. Phenylacetylcarbinol - Wikipedia

    en.wikipedia.org/wiki/Phenylacetylcarbinol

    The majority of L-PAC is generated in pharmaceutical plants in India, as an intermediate precursor in the production of pseudoephedrine. There are also biochemical reactions where enzymes such as acetohydroxyacid synthase I from E. coli condense pyruvate and benzaldehyde into R-PAC. Such methods have much higher conversion rates in comparison ...

  9. N-Methylpseudoephedrine - Wikipedia

    en.wikipedia.org/wiki/N-Methylpseudoephedrine

    Download as PDF; Printable version; In other projects Wikidata item; Appearance. ... It is a derivative of pseudoephedrine and an isomer of N-methylephedrine.

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