Results 331 to 340 of about 55,807 (381)
Some of the next articles are maybe not open access.
Toxicology and Applied Pharmacology, 2000
The catechol metabolites of estradiol, 2- and 4-hydroxyestradiol (2-OHE(2) and 4-OHE(2), respectively) are potent signaling molecules and are hypothesized to be central to estrogen-linked carcinogenesis. Methylation by catechol-O-methyltransferase (COMT) is the principal means of catechol estrogen (CE) deactivation in the liver and other tissues.
C E, Garner +3 more
openaire +2 more sources
The catechol metabolites of estradiol, 2- and 4-hydroxyestradiol (2-OHE(2) and 4-OHE(2), respectively) are potent signaling molecules and are hypothesized to be central to estrogen-linked carcinogenesis. Methylation by catechol-O-methyltransferase (COMT) is the principal means of catechol estrogen (CE) deactivation in the liver and other tissues.
C E, Garner +3 more
openaire +2 more sources
Movement Disorders, 2010
AbstractA brief history of the evolution of the term catechol amine and relationship to the treatment of Parkinson's disease.
openaire +2 more sources
AbstractA brief history of the evolution of the term catechol amine and relationship to the treatment of Parkinson's disease.
openaire +2 more sources
Catechol estrogen methylene ethers
Steroids, 1974Abstract We have prepared 2-hydroxyestrone 2,3-methylene ether and 2-hydroxy-estradiol 2,3-methylene ether; these compounds were not found as urinary metabolites of radioactive estrone, estradiol or 2-methoxyestrone in humans.
A M, Femino +3 more
openaire +2 more sources
Catechol Monoglyceryl Ether Carbamates
Journal of Pharmaceutical Sciences, 1963Abstract A series of carbamates and N-methylcarbamates derived from 3-(o-hydroxyphen-oxy)-1,2-propanediol was prepared and screened for muscle relaxant activity. An ester interchange between the above diol and diethyl carbonate failed to give 4-(e-hydroxyphenoxymethyl)-1,3-dioxolone-2; 2-hydroxymethyl-1,4-benzodioxane was obtained instead.
J, SWIDINSKY, J, KERVENSKI, B B, BROWN
openaire +2 more sources
Nucleophilic Deoxyfluorination of Catechols
Organic Letters, 2011Nucleophilic deoxyfluorinaiton of one of the two hydroxyl groups of catechols has been developed via the Umpolung concept. This method was successively applied to naturally occurring catechols, such as catechins and dopamine, to produce novel fluorinated analogues.
Hiroyuki, Nemoto +2 more
openaire +2 more sources
Acta Histochemica, 1977
Summary When catechol, the simplest o-dihydroxy aromatic compound, is oxidized in the presence of potassium alum, there results a solution which stains very similarly to an alum hematoxylin.
openaire +2 more sources
Summary When catechol, the simplest o-dihydroxy aromatic compound, is oxidized in the presence of potassium alum, there results a solution which stains very similarly to an alum hematoxylin.
openaire +2 more sources
Alkylation of catechol with cyclohexene. Novel sterically hindered o-quinones and catechols
Russian chemical bulletin, 2020T. N. Kocherova +8 more
semanticscholar +1 more source

