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  2. Phenethylamine - Wikipedia

    en.wikipedia.org/wiki/Phenethylamine

    [3] [27] [28] Two reviews noted a study where the mean 24 hour urinary phenylacetic acid concentration following just 30 minutes of intense exercise rose 77% above its base level; [3] [27] [28] the reviews suggest that phenethylamine synthesis sharply increases during physical exercise during which it is rapidly metabolized due to its short ...

  3. 1-Phenylethylamine - Wikipedia

    en.wikipedia.org/wiki/1-Phenylethylamine

    1-Phenylethylamine (1-PEA or α-PEA), also known as α-methylbenzylamine, is the organic compound with the formula C 6 H 5 CH(NH 2)CH 3. This primary amine is a colorless liquid is often used in chiral resolutions. Like benzylamine, it is relatively basic and forms stable ammonium salts and imines.

  4. Phenylisobutylamine - Wikipedia

    en.wikipedia.org/wiki/Phenylisobutylamine

    Phenylisobutylamine, also known as α-ethylphenethylamine (AEPEA) or as butanphenamine (B), is a stimulant drug of the phenethylamine and amphetamine families. [1] [2] [3] It is a higher homologue of amphetamine, differing from amphetamine's molecular structure only by the substitution of the methyl group at the alpha position of the side chain with an ethyl group.

  5. List of naturally occurring phenethylamines - Wikipedia

    en.wikipedia.org/wiki/List_of_naturally...

    Tyramine is a phenethylamine that occurs widely in plants [1] and animals, and is metabolized by various enzymes, including monoamine oxidases. Substituted phenethylamines like mescaline and lophophine are found in psychoactive cactus .

  6. N,N-Dimethyl-2-chloro-2-phenylethylamine - Wikipedia

    en.wikipedia.org/wiki/N,N-Dimethyl-2-chloro-2...

    N,N-Dimethyl-2-chloro-2-phenylethylamine (DMEA) is chemical compound that irreversibly inhibits the enzyme acetylcholinesterase. DMEA can cause intoxication in cats, resulting in respiratory failure to death, and progressive damage to the central nervous system in rats. [ 1 ]

  7. Substituted phenethylamine - Wikipedia

    en.wikipedia.org/wiki/Substituted_phenethylamine

    Substituted phenethylamines (or simply phenethylamines) are a chemical class of organic compounds that are based upon the phenethylamine structure; [note 1] the class is composed of all the derivative compounds of phenethylamine which can be formed by replacing, or substituting, one or more hydrogen atoms in the phenethylamine core structure with substituents.

  8. 4-Methylphenethylamine - Wikipedia

    en.wikipedia.org/wiki/4-Methylphenethylamine

    4-Methylphenethylamine (4MPEA), also known as para-methylphenethylamine, is an organic compound with the chemical formula of C 9 H 13 N.4MPEA is a human trace amine associated receptor 1 (TAAR1) agonist, [2] a property which it shares with its monomethylated phenethylamine isomers, such as amphetamine (α-methylphenethylamine), β-methylphenethylamine, and N-methylphenethylamine (a trace amine).

  9. 2-Methylphenethylamine - Wikipedia

    en.wikipedia.org/wiki/2-Methylphenethylamine

    2-Methylphenethylamine (2MPEA) is an organic compound with the chemical formula of C 9 H 13 N. 2MPEA is a human trace amine associated receptor 1 (TAAR1) agonist, [3] a property which it shares with its monomethylated phenethylamine isomers, such as amphetamine (α-methylphenethylamine), β-methylphenethylamine, and N-methylphenethylamine (a trace amine).