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  2. Phenylephrine - Wikipedia

    en.wikipedia.org/wiki/Phenylephrine

    Common side effects when taken by mouth or injected include nausea, vomiting, headache, and anxiety. [12] Use on hemorrhoids is generally well tolerated. [12] Severe side effects may include a slow heart rate, intestinal ischemia, chest pain, kidney failure, and tissue death at the site of injection.

  3. Phenylpropanolamine - Wikipedia

    en.wikipedia.org/wiki/Phenylpropanolamine

    Side effects of phenylpropanolamine include increased heart rate and blood pressure. [13] [14] [15] [12] Rarely, PPA has been associated with hemorrhagic stroke. [11] [16] [13] PPA acts as a norepinephrine releasing agent, indirectly activating adrenergic receptors. [17] [18] [19] As such, it is an indirectly acting sympathomimetic.

  4. Phenylalanine - Wikipedia

    en.wikipedia.org/wiki/Phenylalanine

    Phenylalanine ball and stick model spinning. Phenylalanine (symbol Phe or F) [3] is an essential α-amino acid with the formula C 9 H 11 NO 2.It can be viewed as a benzyl group substituted for the methyl group of alanine, or a phenyl group in place of a terminal hydrogen of alanine.

  5. Phenylketonuria - Wikipedia

    en.wikipedia.org/wiki/Phenylketonuria

    Toxic levels of phenylalanine, along with insufficient levels of tyrosine, can interfere with infant development in ways that have permanent effects. The disease may present clinically with seizures , hypopigmentation (excessively fair hair and skin), and a "musty odor" to the baby's sweat and urine (due to phenylacetate , a carboxylic acid ...

  6. Catecholamine - Wikipedia

    en.wikipedia.org/wiki/Catecholamine

    The amino acids phenylalanine and tyrosine are precursors for catecholamines. Both amino acids are found in high concentrations in blood plasma and the brain. In mammals, tyrosine can be formed from dietary phenylalanine by the enzyme phenylalanine hydroxylase, found in large amounts in the liver.

  7. Lac-Phe - Wikipedia

    en.wikipedia.org/wiki/Lac-Phe

    In mammals it is created from -lactate and L-phenylalanine by the cytosol nonspecific dipeptidase (CNDP2) protein. [1] It is classified as N-acyl-alpha-amino acid and pseudodipeptide. [11] It has also been reported that as an additive, N-L-lactoyl phenylalanine improves the taste of food, conferring an umami flavor. [12]

  8. L-DOPA - Wikipedia

    en.wikipedia.org/wiki/L-DOPA

    l-DOPA is produced from the amino acid l-tyrosine by the enzyme tyrosine hydroxylase. l-DOPA can act as an l-tyrosine mimetic and be incorporated into proteins by mammalian cells in place of l-tyrosine, generating protease-resistant and aggregate-prone proteins in vitro and may contribute to neurotoxicity with chronic l-DOPA administration. [10]

  9. Atropine - Wikipedia

    en.wikipedia.org/wiki/Atropine

    Similar electrophysiological effects also occur at the AV node; however, in this tissue, these changes are manifested as a reduction in impulse conduction velocity through the AV node (negative dromotropy). In the resting state, there is a large degree of vagal tone in the heart, which is responsible for low resting heart rates.

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