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  2. Trihydroxybenzenes - Wikipedia

    en.wikipedia.org/wiki/Trihydroxybenzenes

    The enzyme pyrogallol hydroxytransferase uses benzene-1,2,3,5-tetrol and benzene-1,2,3-triol (pyrogallol), whereas its two products are benzene-1,3,5-triol (phloroglucinol) and benzene-1,2,3,5-tetrol. This enzyme can be found in Pelobacter acidigallici. [2] [3]

  3. Tetrahydroxybenzenes - Wikipedia

    en.wikipedia.org/wiki/Tetrahydroxybenzenes

    Toggle the table of contents. Tetrahydroxybenzenes. 4 languages. ... 1,2,4,5-Tetrahydroxybenzene Structural Formula: CAS Registry Number: 642-96-6 634-94-6 636-32-8

  4. 1,2,3,5-Tetrahydroxybenzene - Wikipedia

    en.wikipedia.org/wiki/1,2,3,5-Tetrahydroxybenzene

    It is a metabolite in the degradation of 3,4,5-trihydroxybenzoate (gallic acid) by Eubacterium oxidoreducens. [ 1 ] The enzyme pyrogallol hydroxytransferase uses 1,2,3,5-tetrahydroxybenzene and 1,2,3-trihydroxybenzene ( pyrogallol ), whereas its two products are 1,3,5-trihydroxybenzene ( phloroglucinol ) and 1,2,3,5-tetrahydroxybenzene.

  5. Genotoxicity - Wikipedia

    en.wikipedia.org/wiki/Genotoxicity

    Genotoxicity is the property of chemical agents that damage the genetic information within a cell causing mutations, which may lead to cancer. While genotoxicity is often confused with mutagenicity, all mutagens are genotoxic, but some genotoxic substances are not mutagenic. The alteration can have direct or indirect effects on the DNA: the ...

  6. Benzene - Wikipedia

    en.wikipedia.org/wiki/Benzene

    In the body, benzene is enzymatically converted to a series of oxidation products including muconic acid, phenylmercapturic acid, phenol, catechol, hydroquinone and 1,2,4-trihydroxybenzene. Most of these metabolites have some value as biomarkers of human exposure, since they accumulate in the urine in proportion to the extent and duration of ...

  7. 2-hydroxy-1,4-benzoquinone reductase - Wikipedia

    en.wikipedia.org/wiki/2-hydroxy-1,4-benzoquinone...

    The 3 substrates of this enzyme are 2-hydroxy-1,4-benzoquinone, NADH, and H +, whereas its two products are 1,2,4-trihydroxybenzene and NAD +. This enzyme participates in gamma-hexachlorocyclohexane degradation and 1,4-dichlorobenzene degradation .

  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. Pyrogallol hydroxytransferase - Wikipedia

    en.wikipedia.org/wiki/Pyrogallol_hydroxytransferase

    Thus, the two substrates of this enzyme are 1,2,3,5-tetrahydroxybenzene and 1,2,3-trihydroxybenzene (pyrogallol), whereas its two products are 1,3,5-trihydroxybenzene (phloroglucinol) and 1,2,3,5-tetrahydroxybenzene. This enzyme participates in benzoic acid degradation via CoA ligation.

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