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  2. Resorcinol - Wikipedia

    en.wikipedia.org/wiki/Resorcinol

    Resorcinol (or resorcin) is a phenolic compound. It is an organic compound with the formula C 6 H 4 (OH) 2. It is one of three isomeric benzenediols, the 1,3-isomer (or meta-isomer). Resorcinol crystallizes from benzene as colorless needles that are readily soluble in water, alcohol, and ether, but insoluble in chloroform and carbon disulfide. [6]

  3. 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]

  4. Phytotoxicity - Wikipedia

    en.wikipedia.org/wiki/Phytotoxicity

    Phytotoxicity describes any adverse effects on plant growth, physiology, or metabolism caused by a chemical substance, such as high levels of fertilizers, herbicides, heavy metals, or nanoparticles. [1] General phytotoxic effects include altered plant metabolism, growth inhibition, or plant death. [2]

  5. Alkylresorcinol - Wikipedia

    en.wikipedia.org/wiki/Alkylresorcinol

    Increasing evidence from human intervention trials suggests that they are the most promising biomarker of whole grain wheat and rye intake. [16] [17] Alkylresorcinol metabolites, 3,5-dihydroxybenzoic acid (DHBA) and 3,5-dihydroxyphenylpropionoic acid (DHPPA) were first identified in urine [18] and can be quantified in urine [19] and plasma, [20] and may be an alternative, equivalent biomarker ...

  6. Catechin - Wikipedia

    en.wikipedia.org/wiki/Catechin

    Catechin possesses two benzene rings (called the A and B rings) and a dihydropyran heterocycle (the C ring) with a hydroxyl group on carbon 3. The A ring is similar to a resorcinol moiety while the B ring is similar to a catechol moiety. There are two chiral centers on the molecule on carbons 2 and 3. Therefore, it has four diastereoisomers.

  7. Resveratrol - Wikipedia

    en.wikipedia.org/wiki/Resveratrol

    Resveratrol (3,5,4′-trihydroxy-trans-stilbene) is a stilbenoid, a type of natural phenol or polyphenol and a phytoalexin produced by several plants in response to injury or when the plant is under attack by pathogens, such as bacteria or fungi.

  8. Naturally occurring phenols - Wikipedia

    en.wikipedia.org/wiki/Naturally_occurring_phenols

    Juglone is an example of such a molecule inhibiting the growth of other plant species around walnut trees. [citation needed] The aquatic vascular plant Myriophyllum spicatum produces ellagic, gallic and pyrogallic acids and (+)-catechin, allelopathic phenolic compounds inhibiting the growth of blue-green alga Microcystis aeruginosa. [59]

  9. 1,4-Benzoquinone - Wikipedia

    en.wikipedia.org/wiki/1,4-Benzoquinone

    1,4-Benzoquinone is a toxic metabolite found in human blood and can be used to track exposure to benzene or mixtures containing benzene and benzene compounds, such as petrol. [25] The compound can interfere with cellular respiration, and kidney damage has been found in animals receiving severe exposure.