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  2. 1,3-Cyclohexanedione - Wikipedia

    en.wikipedia.org/wiki/1,3-Cyclohexanedione

    1,3-Cyclohexanedione is an organic compound with the formula (CH 2) 4 (CO) 2. It is one of three isomeric cyclohexanediones. It is a colorless compound that occurs ...

  3. Cyclohexane-1,3-dione hydrolase - Wikipedia

    en.wikipedia.org/wiki/Cyclohexane-1,3-dione...

    In enzymology, a cyclohexane-1,3-dione hydrolase (EC 3.7.1.10) is an enzyme that catalyzes the chemical reaction cyclohexane-1,3-dione + H 2 O ⇌ {\displaystyle \rightleftharpoons } 5-oxohexanoate Thus, the two substrates of this enzyme are cyclohexane-1,3-dione and H 2 O , whereas its product is 5-oxohexanoate .

  4. Deamination - Wikipedia

    en.wikipedia.org/wiki/Deamination

    Deamination is the removal of an amino group from a molecule. [1] Enzymes that catalyse this reaction are called deaminases. In the human body, deamination takes place primarily in the liver; however, it can also occur in the kidney. In situations of excess protein intake, deamination is used to break down amino acids for energy.

  5. Cyclohexanedione - Wikipedia

    en.wikipedia.org/wiki/Cyclohexanedione

    1,3-Cyclohexanedione; 1,4-Cyclohexanedione This page was last edited on 23 June 2017, at 01:22 (UTC). Text is available under the Creative Commons Attribution ...

  6. Dimedone - Wikipedia

    en.wikipedia.org/wiki/Dimedone

    Dimedone is an organic compound with the formula (CH 3) 2 C(CH 2) 2 (CO) 2 (CH 2). Classified as a cyclic diketone, it is a derivative of 1,3-cyclohexanedione. It is a white solid that is soluble in water, as well as ethanol and methanol. It once was used as a reagent to test for the aldehyde functional group.

  7. Hydrolase - Wikipedia

    en.wikipedia.org/wiki/Hydrolase

    Hydrolases are classified as EC 3 in the EC number classification of enzymes. Hydrolases can be further classified into several subclasses, based upon the bonds they act upon: Hydrolases can be further classified into several subclasses, based upon the bonds they act upon:

  8. Cyclohexa-1,3-diene - Wikipedia

    en.wikipedia.org/wiki/Cyclohexa-1,3-diene

    Cyclohexa-1,3-diene itself is rare in nature, but the cyclohexa-1,3-diene motif is fairly common. [8] One example is chorismic acid , an intermediate in the shikimic acid pathway . Of the several examples of the terpenoids and terpenes , a prominent example is phellandrene .

  9. Drug metabolism - Wikipedia

    en.wikipedia.org/wiki/Drug_metabolism

    Drug metabolism is the metabolic breakdown of drugs by living organisms, usually through specialized enzymatic systems. More generally, xenobiotic metabolism (from the Greek xenos "stranger" and biotic "related to living beings") is the set of metabolic pathways that modify the chemical structure of xenobiotics, which are compounds foreign to an organism's normal biochemistry, such as any drug ...