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  2. Ephedrine - Wikipedia

    en.wikipedia.org/wiki/Ephedrine

    Ephedrine works by inducing the release of norepinephrine and hence indirectly activating the α-and β-adrenergic receptors. [11] Chemically, ephedrine is a substituted amphetamine and is the (1R,2S)-enantiomer of β-hydroxy-N-methylamphetamine. [14] Ephedrine was first isolated in 1885 and came into commercial use in 1926.

  3. Precursor chemicals - Wikipedia

    en.wikipedia.org/wiki/Precursor_chemicals

    Drug precursors, also referred to as precursor chemicals or simply precursors, are substances used to manufacture illicit drugs. Most precursors also have legitimate commercial uses and are legally used in a wide variety of industrial processes and consumer products, such as medicines, flavourings, and fragrances.

  4. History and culture of substituted amphetamines - Wikipedia

    en.wikipedia.org/wiki/History_and_culture_of...

    (The hydrogen iodide is replaced by iodine and water in the "Moscow route".) [107] The hydrogen iodide is used to reduce either ephedrine or pseudoephedrine to methamphetamine. [101] On heating, the precursor is rapidly iodinated by the hydrogen iodide to form iodoephedrine.

  5. Amphetamine type stimulant - Wikipedia

    en.wikipedia.org/wiki/Amphetamine_type_stimulant

    Ephedrine is the precursor of synthetic amphetamines. The diastereomer of ephedrine, pseudoephedrine is found in Ephedra sinica together along with ephedrine. Ephedrine and pseudoephedrine are both generally used for weight reduction and performance enhancement. They can also be reduced to methamphetamine. [2]

  6. DEA list of chemicals - Wikipedia

    en.wikipedia.org/wiki/DEA_list_of_chemicals

    The United States Drug Enforcement Administration (DEA) maintains lists regarding the classification of illicit drugs (see DEA Schedules).It also maintains List I of chemicals and List II of chemicals, which contain chemicals that are used to manufacture the controlled substances/illicit drugs.

  7. Alkaloid - Wikipedia

    en.wikipedia.org/wiki/Alkaloid

    Biological precursors of most alkaloids are amino acids, such as ornithine, lysine, phenylalanine, tyrosine, tryptophan, histidine, aspartic acid, and anthranilic acid. [188] Nicotinic acid can be synthesized from tryptophan or aspartic acid. Ways of alkaloid biosynthesis are too numerous and cannot be easily classified. [85]

  8. Phenylpropanolamine - Wikipedia

    en.wikipedia.org/wiki/Phenylpropanolamine

    Ephedrine is the N-methyl analogue of phenylpropanolamine. Exogenous compounds in this family are degraded too rapidly by monoamine oxidase to be active at all but the highest doses. [51] However, the addition of the α-methyl group allows the compound to avoid metabolism and confer an effect. [51]

  9. Ephedra (plant) - Wikipedia

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

    Ephedra is the origin of the name of the stimulant ephedrine, ... Ephedra has also had a role as a precursor in the clandestine manufacture of methamphetamine.