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Related to salicyl: salicyl alcohol


The acyl radical of salicylic acid.
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The result showed that the components were formaldehyde, hydrazine, 1,2-dimethyl-, acetic acid, 2-isopropoxyethylamine, formic acid, acetic acid, phenol, benzaldehyde, 2-hydroxy-, phenol, 4-methyl-, benzoic acid, 2-furancarboxaldehyde, 5-(hydroxymethyl)-, methenamine, salicyl alcohol, phenol, 2,6-dimethoxy-, benzaldehyde, 3-hydroxy 4-methoxy-, phenol, 2-methoxy-4-(1-propenyl)-(e), ethanone, 1-(4-hydroxy-3-methoxyphenyl)-, phenol, 2,4-bis(1,1-dimethylethyl), benzeneacetic acid, 4-hydroxy-3-methoxy-, methyl ester, phenol, 2,6-dimethoxy-4-(2-propenyl)-, pentadecane, 2,6,10,14-tetramethyl, ethanol, 2-(dodecyloxy)-, phthalic acid, isobutyl nonyl ester, 1,4-dimethyl-8-isopropylidenetricyclo[,10)]decane.
En esta estacion reaparece el fenol Butylated hydroxytoluene - BHT, el cual estaba presente en la Estacion 1; el Salicyl Alcohol registra irritaciones cutaneas y oculares (Categoria 2), toxicidad especifica en determinados organos - exposicion unica (Categoria 3); y el Phen-1,4-diol, 2,3-dimethyl-5-trifluoromethyl, no registra informacion de toxicidad y bio-actividad en la base de datos PubChem Compound.
Currently we have reported the anti- inflammatory, anti-nociceptive and anti-pyretic activity of bioisosterically synthesized nitrogen containing derivatives of salicyl alcohol with no propensity of gastric ulceration as compared to aspirin [9-10].
The FRs were characterized by a high content of flavone and chalcone glycosides (FR-B), flavonoid glycosides and salicyl alcohol derivatives (FR-C), salicin and related salicyl alcohol derivatives (FR-D) and proanthocyanidines (FR-E).
Potentiation by salicylate and salicyl alcohol of cadmium toxicity and accumulation in Escherichia coil Appl Environ Microbiol 34:2402-2406.
Only the naphthyl and salicyl derivatives gave substantial amounts (5-58%) of the corresponding monoamines as detected by [sup.13]C NMR spectroscopy.
Alkyl and aryl-substituted salicyl phosphates as detection reagents in enzyme amplified fluorescence DNA hybridization assays on solid support.
The larvae of these beetles convert salicyl glucosides (SGs) from the leaves of their host plants into a defensive secretion, which consists mostly of salicylaldehyde (Pasteels et al.
They include: glucosides, such as salicin, populin, tremuloidin, salireposide, and grandidentatin; acids such as benzoic and p-hydroxybenzoic; and phenols, such as salicyl alcohol and catechol[9].
Despite the mentioned intramolecular hydrogen interactions and a partial conjugation of the molecule, this one is not planar, probably due to the packing based on the intermolecular hydrogen bonds and the [pi]-stacking interactions between the salicyl residues of the neighbouring molecules (see Figure 6).
As this process is also mentionable in vivo for all compounds exhibiting a cyclohexenon carboxylic acid moiety, like the salicyl alcohol derivatives salicortin, 2'-acetylsalicortin and tremulacin (Poblecka-Olech et al.
The salicin and salicyl alcohol content was determined according Ph.Eur 6.4, total polyphenol, tannin and rest phenol content was quantified according to Glasl (1983).