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1986 2
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2001 1
2003 1
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2006 2
2008 1
2011 1
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2017 5
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29 results

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Page 1
Characterization of the action of tyrosinase on resorcinols.
Garcia-Jimenez A, Teruel-Puche JA, Berna J, Rodriguez-Lopez JN, Tudela J, Garcia-Ruiz PA, Garcia-Canovas F. Garcia-Jimenez A, et al. Bioorg Med Chem. 2016 Sep 15;24(18):4434-4443. doi: 10.1016/j.bmc.2016.07.048. Epub 2016 Jul 22. Bioorg Med Chem. 2016. PMID: 27480027
The action of tyrosinase on resorcinol and some derivatives (4-ethylresorcinol, 2-methylresorcinol and 4-methylresorcinol) was investigated. If the catalytic cycle is completed with a reductant such as ascorbic acid or an o-diphenol such as 4-tert-butylcatechol, the …
The action of tyrosinase on resorcinol and some derivatives (4-ethylresorcinol, 2-methylresorcinol and 4-methylresorcinol) was …
2-Alkenal-scavenging ability of m-diphenols.
Hidalgo FJ, Zamora R. Hidalgo FJ, et al. Food Chem. 2014 Oct 1;160:118-26. doi: 10.1016/j.foodchem.2014.03.071. Epub 2014 Mar 22. Food Chem. 2014. PMID: 24799217
The reaction between m-diphenols (resorcinol, 2-methylresorcinol, 2,5-dimethylresorcinol, 3-methylphenol, orcinol, and phloroglucinol) and 2-alkenals (2-pentenal and 2-octenal) was studied in an attempt to understand the chemical pathways involved in the scav …
The reaction between m-diphenols (resorcinol, 2-methylresorcinol, 2,5-dimethylresorcinol, 3-methylphenol, orcinol, and …
Complexation equilibria between niobium(V) and 4-(4'H-1',2',4'-triazolyl-3'-azo)-2-methylresorcinol Extraction-spectrophotometric determination of niobium in pyrochlore-bearing rocks.
Sánchez MJ, Francisco A, Jiménez F, Montelongo FG. Sánchez MJ, et al. Talanta. 1989 Aug;36(8):831-6. doi: 10.1016/0039-9140(89)80163-8. Talanta. 1989. PMID: 18964815
The complexation equilibria between niobium(V) and 4-(1'H-1',2',4'-triazolyl-3'-azo)-2-methylresorcinol has been studied by spectrophotometric methods and graphical and numerical calculation methods. ...
The complexation equilibria between niobium(V) and 4-(1'H-1',2',4'-triazolyl-3'-azo)-2-methylresorcinol has been studied by sp …
A subchronic, teratologic, and dominant lethal study of 2-methylresorcinol in rats. II. Teratologic and dominant lethal study.
Re TA, Loehr RF, Rodriguez SC, Rodwell DE, Burnett CM. Re TA, et al. Fundam Appl Toxicol. 1986 Aug;7(2):293-8. doi: 10.1016/0272-0590(86)90159-4. Fundam Appl Toxicol. 1986. PMID: 3758547
2-Methylresorcinol (2-MR) was administered to groups of 40 male and 35 female Sprague-Dawley rats by admixture with the diets at levels of 0.1, 0.4, and 1.5% (see Part I; T.H. ...
2-Methylresorcinol (2-MR) was administered to groups of 40 male and 35 female Sprague-Dawley rats by admixture with the
Epoxyalkenal-trapping ability of phenolic compounds.
Zamora R, Aguilar I, Hidalgo FJ. Zamora R, et al. Food Chem. 2017 Dec 15;237:444-452. doi: 10.1016/j.foodchem.2017.05.129. Epub 2017 May 26. Food Chem. 2017. PMID: 28764018
In an attempt to fill this gap, the reactions of 4,5-epoxy-2-hexenal, 4,5-epoxy-2-heptenal, and 4,5-epoxy-2-decenal, with 2-methylresorcinol and 2,5-dimethylresorcinol were studied. These reactions produced diverse 1,3a,4,9b-tetrahydro-2H-furo[2,3-c]chromene-2,7-dio …
In an attempt to fill this gap, the reactions of 4,5-epoxy-2-hexenal, 4,5-epoxy-2-heptenal, and 4,5-epoxy-2-decenal, with 2-methyl
2,4-Alkadienal trapping by phenolics.
Hidalgo FJ, Zamora R. Hidalgo FJ, et al. Food Chem. 2018 Oct 15;263:89-95. doi: 10.1016/j.foodchem.2018.04.121. Epub 2018 Apr 28. Food Chem. 2018. PMID: 29784333
In an attempt to clarify the trapping of 2,4-alkadienals by phenolics, this study analyzes the reactions of 2,4-hexadienal, 2,4-heptadienal, and 2,4-decadienal with 2-methylresorcinol. These reactions produced (E)-4-(alk-1-en-1-yl)-8-methyl-2,7-bis(prop-1-en-2-yloxy …
In an attempt to clarify the trapping of 2,4-alkadienals by phenolics, this study analyzes the reactions of 2,4-hexadienal, 2,4-heptadienal, …
Synthesis of a series of aromatic benziporphyrins and heteroanalogues via tripyrrane-like intermediates derived from resorcinol and 2-methylresorcinol.
Lash TD, Miyake K, Xu L, Ferrence GM. Lash TD, et al. J Org Chem. 2011 Aug 5;76(15):6295-308. doi: 10.1021/jo201098c. Epub 2011 Jul 5. J Org Chem. 2011. PMID: 21692522
Tripyrrane analogues were prepared by reacting resorcinol or 2-methylresorcinol with 2 equiv of an acetoxymethylpyrrole in the presence of p-toluenesulfonic acid and calcium chloride. ...
Tripyrrane analogues were prepared by reacting resorcinol or 2-methylresorcinol with 2 equiv of an acetoxymethylpyrrole in the …
Preparation of tripyrrane analogues from resorcinol and 2-methylresorcinol for applications in the synthesis of new benziporphyrin systems.
Miyake K, Lash TD. Miyake K, et al. Chem Commun (Camb). 2004 Jan 21;(2):178-9. doi: 10.1039/b313229n. Epub 2003 Dec 8. Chem Commun (Camb). 2004. PMID: 14737537
Acid catalyzed condensation of resorcinol or 2-methylresorcinol with 2 equiv. of an acetoxymethylpyrrole gave bis(pyrrolylmethyl)benzene derivatives in moderate yields; these afforded a series of novel aromatic benziporphyrins using the MacDonald "3 + 1" methodology …
Acid catalyzed condensation of resorcinol or 2-methylresorcinol with 2 equiv. of an acetoxymethylpyrrole gave bis(pyrrolylmeth …
A subchronic, teratologic, and dominant lethal study of 2-methylresorcinol in rats. I. Subchronic toxicity.
Re TA, Loehr RF, Rodriguez SC, Gilmore CE, Burnett CM. Re TA, et al. Fundam Appl Toxicol. 1986 Aug;7(2):287-92. doi: 10.1016/0272-0590(86)90158-2. Fundam Appl Toxicol. 1986. PMID: 3758546
2-methylresorcinol (2-MR) was administered to groups of 40 male and 35 female Sprague-Dawley rats by admixture with diets at levels of 0.1, 0.4, and 1.5% for periods up to 6 months. ...
2-methylresorcinol (2-MR) was administered to groups of 40 male and 35 female Sprague-Dawley rats by admixture with die
Phenolic trapping of lipid oxidation products 4-oxo-2-alkenals.
Hidalgo FJ, Aguilar I, Zamora R. Hidalgo FJ, et al. Food Chem. 2018 Feb 1;240:822-830. doi: 10.1016/j.foodchem.2017.08.027. Epub 2017 Aug 5. Food Chem. 2018. PMID: 28946347
The reaction between 4-oxo-2-alkenals (fumaraldehyde, 4-oxo-2-hexenal, and 4-oxo-2-nonenal) and phenolic compounds (resorcinol and 2-methylresorcinol) was studied to characterize the trapping ability of phenolic compounds for these lipid oxidation products. ...
The reaction between 4-oxo-2-alkenals (fumaraldehyde, 4-oxo-2-hexenal, and 4-oxo-2-nonenal) and phenolic compounds (resorcinol and 2- …
29 results