Results 181 to 190 of about 319,930 (224)
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Mechanism of catechol estrogen formation in man
Steroids, 1973Abstract Following the administration of estrone- 3 H-sulfate- 35 S to man, estrone sulfate, 2-methoxyestrone sulfate and 2-hydroxyestrone-2-sulfate were isolated from urine and purified. Their isotope content showed that estrone sulfate and 2-methoxyestrone sulfate retained 23 and 21% of the originally present 35 S, while 2-hydroxyestrone estrone ...
J, Fishman, I, Yoshizawa, L, Hellman
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Convenient large scale preparation of catechol estrogens
Steroids, 19762-Hydroxyestrone, 2-hydroxyestradiol-17beta, 2-hydroxy-17alpha-ethynylestradiol, 2-hydroxyestriol, 4-hydroxyestrone, 4-hydroxyestradiol-17beta, 4-hydroxy-17alpha-ethynylestradiol and 4-hydroxyestriol are prepared on a preparative scale from the corresponding aminophenols using a new inverse oxidation procedure.
G, Stubenrauch, R, Knuppen
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Cimetidine inhibits catechol estrogen metabolism in women
Maturitas, 1991Chronic cimetidine use in men is associated with hyperestrogenic side effects such as gynecomastia, which may be linked to inhibition of estradiol 2-hydroxylation. As this property of the drug might be helpful in hypoestrogenic states such as osteoporosis, we investigated the effect of cimetidine on estradiol metabolism in premenopausal and ...
J J, Michnovicz, R A, Galbraith
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Gas chromatography/mass spectrometry of catechol estrogens
Steroids, 1992Catecholestrogens (CCEs), namely 2- or 4-hydroxyestradiol and hydroxyestrone, are highly polar, reactive, and extremely labile estrogen metabolites in many experimental conditions. For these reasons, indirect assay methods mainly have been used. Some experimental evidence suggests that CCEs are synthesized and biologically active mostly in target cells.
L A, Castagnetta +5 more
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Regioselective reaction of thiols with catechol estrogens and estrogen-O-quinones
Journal of Steroid Biochemistry, 1986Incubations of [3H]estradiol and [3H]2-hydroxyestradiol (2-OHE2) with rat liver microsomes and mushroom tyrosinase were carried out in the presence of glutathione and 2-mercaptoethanol. A ratio of about 3.5:1 for the C-4 and C-1 thioether conjugates of 2-OHE2 was observed.
Y J, Abul-Hajj, P L, Cisek
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Journal of Clinical Endocrinology and Metabolism, 1972
P. Ball, R. Knuppen, M. Haupt, H. Breuer
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P. Ball, R. Knuppen, M. Haupt, H. Breuer
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Nihon rinsho. Japanese journal of clinical medicine, 1985
S, Takagi, M, Saito
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S, Takagi, M, Saito
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Catechol estrogens induce proliferation and malignant transformation in prostate epithelial cells.
Toxicology Letters, 2013H. Mosli +3 more
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