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Pyrogallol is an organic compound with the formula C 6 H 3 (OH) 3. It is a water-soluble, white solid although samples are typically brownish because of its sensitivity toward oxygen. [ 3 ] It is one of three isomers of benzenetriols .
1,2,3,5-Tetrahydroxybenzene, also known as pyrogallol, has various uses. It is used in the production of certain dyes, photographic developers, and hair dyes. Additionally, pyrogallol has been employed in traditional medicine and some cosmetic formulations due to its antioxidant properties.
A hydrolysable tannin or pyrogallol-type tannin is a type of tannin that, on heating with hydrochloric or sulfuric acids, yields gallic or ellagic acids. [ 1 ] At the center of a hydrolysable tannin molecule , there is a carbohydrate (usually D-glucose but also cyclitols like quinic or shikimic acids ).
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.
In enzymology, a pyrogallol 1,2-oxygenase (EC 1.13.11.35) is an enzyme that catalyzes the chemical reaction. 1,2,3-trihydroxybenzene + O 2 ...
In some countries and in veterinary medicine, phloroglucinol is used as a treatment for gallstones, spasmodic pain and other related gastrointestinal disorders [17] A 2018 review found insufficient evidence that phloroglucinol was effective for treating abdominal pain [18] A 2020 review found insufficient evidence that phloroglucinol was ...
Medical Care Research and Review is a peer-reviewed academic journal that covers the field of health care. The editor-in-chief is Thomas D'Aunno ( Columbia University Mailman School of Public Health ).
A pyrogallolarene (also calix[4]pyrogallolarene) is a macrocycle, or a cyclic oligomer, based on the condensation of pyrogallol (1,2,3-trihydroxybenzene) and an aldehyde. Pyrogallolarenes are a type of calixarene , and a subset of resorcinarenes that are substituted with a hydroxyl at the 2-position.