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  2. 4-Methylcatechol - Wikipedia

    en.wikipedia.org/wiki/4-methylcatechol

    Calone, a derivative of 4-methylcatechol, is known in the fragrance industry as "watermelon ketone" for its distinctive odor. [3]The brand of low-temperature coke used as a smokeless fuel Coalite obtains homocatechol from ammoniacal liquor by solvent extraction, distillation and crystallisation.

  3. 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 ...

  4. Catechol - Wikipedia

    en.wikipedia.org/wiki/Catechol

    Catechol (/ ˈ k æ t ɪ tʃ ɒ l / or / ˈ k æ t ɪ k ɒ l /), also known as pyrocatechol or 1,2-dihydroxybenzene, is an organic compound with the molecular formula C 6 H 4 (OH) 2. It is the ortho isomer of the three isomeric benzenediols .

  5. Methyltransferase - Wikipedia

    en.wikipedia.org/wiki/Methyltransferase

    SAM is the classical methyl donor for methyltransferases, however, examples of other methyl donors are seen in nature. The general mechanism for methyl transfer is a S N 2 -like nucleophilic attack where the methionine sulfur serves as the leaving group and the methyl group attached to it acts as the electrophile that transfers the methyl group ...

  6. Transferase - Wikipedia

    en.wikipedia.org/wiki/Transferase

    Another example of historical significance relating to transferase is the discovery of the mechanism of catecholamine breakdown by catechol-O-methyltransferase. This discovery was a large part of the reason for Julius Axelrod’s 1970 Nobel Prize in Physiology or Medicine (shared with Sir Bernard Katz and Ulf von Euler). [16]

  7. Piperonal - Wikipedia

    en.wikipedia.org/wiki/Piperonal

    Piperonal can be prepared by the oxidative cleavage of isosafrole or by using a multistep sequence from catechol or 1,2-methylenedioxybenzene.Synthesis from the latter chemical is accomplished through a condensation reaction with glyoxylic acid followed by cleaving the resulting α-hydroxy acid with an oxidizing agent.

  8. Phenylethanolamine N-methyltransferase - Wikipedia

    en.wikipedia.org/wiki/Phenylethanolamine_N...

    It consists of 4 exons and is a 30 kDa protein. It shares many properties found among the other methyltransferases. It is closest in sequence to glycine-N-methyl transferase . It also shares many structural properties like the shape of the folding lip with catechol-O-methyl transferase (COMT), though it shares less sequence identity. Several ...

  9. 4-tert-Butylcatechol - Wikipedia

    en.wikipedia.org/wiki/4-tert-Butylcatechol

    4-tert-Butylcatechol (TBC) is an organic chemical compound which is a derivative of catechol. [1] TBC is available in the form of a solid crystal flake [ 2 ] and 85% solution in methanol [ 3 ] or water.