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  2. Catecholamine - Wikipedia

    en.wikipedia.org/wiki/Catecholamine

    Two catecholamines, norepinephrine and dopamine, act as neuromodulators in the central nervous system and as hormones in the blood circulation. The catecholamine norepinephrine is a neuromodulator of the peripheral sympathetic nervous system but is also present in the blood (mostly through "spillover" from the synapses of the sympathetic system).

  3. C9H10O5 - Wikipedia

    en.wikipedia.org/wiki/C9H10O5

    Ethyl gallate, an antioxidant food additive; Syringic acid, a polyphenol; Vanillylmandelic acid, a catecholamine This page was last edited on 5 September 2024, at 01: ...

  4. Catechol-O-methyltransferase - Wikipedia

    en.wikipedia.org/wiki/Catechol-O-methyltransferase

    Catechol-O-methyltransferase is involved in the inactivation of the catecholamine neurotransmitters (dopamine, epinephrine, and norepinephrine). The enzyme introduces a methyl group to the catecholamine, which is donated by S-adenosyl methionine (SAM). Any compound having a catechol structure, like catecholestrogens and catechol-containing ...

  5. What Are Catecholamines, and What Do They Do?

    www.aol.com/catecholamines-181010080.html

    Examples Are Dopamine and Adrenaline. For premium support please call: 800-290-4726 more ways to reach us

  6. Deoxyepinephrine - Wikipedia

    en.wikipedia.org/wiki/Deoxyepinephrine

    One of the most prominent pharmacological characteristics of epinine, its ability to raise blood pressure, was noted as early as 1910, by Barger and Dale, who reported that "methylamino-ethyl-catechol", as they called it, had about 1/7 x the pressor potency of epinephrine, but about 5 x the potency of dopamine ("amino-ethyl-catechol") in cat preparations. [14]

  7. Phenylalanine - Wikipedia

    en.wikipedia.org/wiki/Phenylalanine

    The latter three are known as the catecholamines. Phenylalanine uses the same active transport channel as tryptophan to cross the blood–brain barrier . In excessive quantities, supplementation can interfere with the production of serotonin and other aromatic amino acids [ 11 ] as well as nitric oxide due to the overuse (eventually, limited ...

  8. Dihydroxybenzenes - Wikipedia

    en.wikipedia.org/wiki/Dihydroxybenzenes

    There are three structural isomers: 1,2-dihydroxybenzene (the ortho isomer) is commonly known as catechol, 1,3-dihydroxybenzene (the meta isomer) is commonly known as resorcinol, and 1,4-dihydroxybenzene (the para isomer) is commonly known as hydroquinone. [1]

  9. Phenylethanolamine - Wikipedia

    en.wikipedia.org/wiki/Phenylethanolamine

    Phenylethanolamine (sometimes abbreviated PEOH), or β-hydroxyphenethylamine, is a trace amine with a structure similar to those of other trace phenethylamines as well as the catecholamine neurotransmitters dopamine, norepinephrine, and epinephrine.