aryl


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aryl

[′ar·əl]
(organic chemistry)
An organic group derived from an aromatic hydrocarbon by removal of one hydrogen.
References in periodicals archive ?
When ICZ binds to and activates the Aryl hydrocarbon receptor (AHR) in the intestinal lining, it aids in maintaining a healthy balance in the gut flora and immune surveillance, and enhances host barrier function, according to the researchers.
Aryl hydrocarbon receptor-mediated induction of Stearoyl-CoA desaturase 1 alters hepatic fatty acid composition in TCDD-elicited steatosis.
The report provides comprehensive information on the Soluble Epoxide Hydrolase (Epoxide Hydratase or Aryl Epoxide Hydrase or EC 3.
Two chemicals (Polyoxyethylene Nonylphenyl Ether and Neutral Calcium Alkyl Aryl Sulfonate) were completely soluble or miscible at 0.
18 August 2014 - US nuclear receptor screening specialist Indigo Biosciences said Monday it had launched a cell-based aryl hydrocarbon receptor (AhR) reporter assay kit for screening test samples to quantify any functional activity that they may exert against human AhR.
Among the topics are the copper-catalyzed formation of carbon-phosphorous bonds with aryl halides, insights into the mechanism of modern Ullmann-Goldberg coupling reactions, copper-catalyzed alkynylation and alkenylation reactions of alkynyl derivatives, applying copper-mediated carbon-nitrogen bond formation in complex molecule synthesis, and reusable catalysts for copper-mediated cross-coupling reactions under heterogeneous conditions.
The ROC fraction was measured as the amount of poly-aryl carbon existing in addition to any aryl C that could be defined as lignin.
In their new approach, the team added compounds that modulate the aryl hydrocarbon receptor (AhR) pathway.
The Sonogashira cross-coupling reaction takes place between aryl halide (ArX) and terminal acetylene, catalysed by a zerovalent palladium catalyst to produce diyne (see Fig.
The aryl hydrocarbon receptor (AhR) is a soluble, ligand-activated transcription factor that mediates the toxic effects of 2,3,7,8-tetrachlorodibenzop-dioxin (TCDD).
Interestingly, the first two agents act as aryl hydrocarbon receptor (AhR) agonists, while DIM does not.
At its core, a Buchwald-Hartwig amination is an aryl halide reacting with an amine [see above example].