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  2. Urolithin A - Wikipedia

    en.wikipedia.org/wiki/Urolithin_A

    Urolithin A is a metabolite compound resulting from the transformation of ellagitannins by the gut bacteria. [1] It belongs to the class of organic compounds known as benzo- coumarins or dibenzo-α- pyrones .

  3. Urolithin - Wikipedia

    en.wikipedia.org/wiki/Urolithin

    Chemical structure of urolithin A.. Urolithins are microflora metabolites of dietary ellagic acid derivatives, such as ellagitannins. [1] They are produced in the gut, and found in the urine in the form of urolithin B glucuronide after absorption of ellagitannins-containing foods, such as pomegranate. [2]

  4. Eating More of This Fruit May Improve Memory and ... - AOL

    www.aol.com/eating-more-fruit-may-improve...

    Experts explain urolithin A and brain health. A substance found in pomegranates may improve memory and Alzheimer’s disease symptoms, new research finds. Experts explain urolithin A and brain health.

  5. Toxication - Wikipedia

    en.wikipedia.org/wiki/Toxication

    Toxication, toxification or toxicity exaltation is the conversion of a chemical compound into a more toxic form in living organisms or in substrates such as soil or water. The conversion can be caused by enzymatic metabolism in the organisms, as well as by abiotic chemical reactions .

  6. Ellagitannin - Wikipedia

    en.wikipedia.org/wiki/Ellagitannin

    Castalagin is a representative ellagitannin, characterized by coupled gallic acid substituents. The ellagitannins are a diverse class of hydrolyzable tannins, a type of polyphenol formed primarily from the oxidative linkage of galloyl groups in 1,2,3,4,6-pentagalloyl glucose.

  7. Toxicity - Wikipedia

    en.wikipedia.org/wiki/Toxicity

    Toxicity is the degree to which a chemical substance or a particular mixture of substances can damage an organism. [1] Toxicity can refer to the effect on a whole organism, such as an animal, bacterium, or plant, as well as the effect on a substructure of the organism, such as a cell (cytotoxicity) or an organ such as the liver (hepatotoxicity).

  8. Hypervitaminosis A - Wikipedia

    en.wikipedia.org/wiki/Hypervitaminosis_A

    The toxic effects of preformed vitamin A might be related to altered vitamin D metabolism, concurrent ingestion of substantial amounts of vitamin D, or binding of vitamin A to receptor heterodimers. Antagonistic and synergistic interactions between these two vitamins have been reported, as they relate to skeletal health.

  9. Talk:Urolithin A - Wikipedia

    en.wikipedia.org/wiki/Talk:Urolithin_A

    The favorable GRAS notice obtained by Amazentis is of interest as it establishes the safety of urolithin A for food products (non-medical). Also, a GRAS notice from the FDA seems to fit the definition of a secondary source. Jules8th 08:30, 25 August 2020 (UTC) Added to the Safety section with the appropriate FDA source.