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Journal articles on the topic 'Α-ethynylestradiol'

Author: Grafiati
Published: 4 June 2021
Last updated: 1 February 2022

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1

Peter Guengerich, F. "Metabolism of 17 α-ethynylestradiol in humans". Life Sciences 47, № 22 (1990): 1981–88. http://dx.doi.org/10.1016/0024-3205(90)90431-p.

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2

Yamamoto, Yukio, Rick Moore, Holly A. Hess та ін. "Estrogen Receptor α Mediates 17α-Ethynylestradiol Causing Hepatotoxicity". Journal of Biological Chemistry 281, № 24 (2006): 16625–31. http://dx.doi.org/10.1074/jbc.m602723200.

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3

Beltrán, F. J., P. Pocostales, P. Alvarez та A. Aguinaco. "Ozone-activated Carbon Mineralization of 17-α-Ethynylestradiol Aqueous Solutions". Ozone: Science & Engineering 31, № 6 (2009): 422–27. http://dx.doi.org/10.1080/01919510903324081.

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4

Arterburn, Jeffrey B., Kalla Venkateswara Rao та Marc C. Perry. "ChemInform Abstract: Novel 17 α-Ethynylestradiol Derivatives: Sonogashira Couplings Using Unprotected Phenylhydrazines." ChemInform 31, № 16 (2010): no. http://dx.doi.org/10.1002/chin.200016203.

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5

Stunges, Gabriele M., Cibely S. Martin, Gilia C. M. Ruiz, Osvaldo N. Oliveira, Carlos J. L. Constantino та Priscila Alessio. "Interaction between 17 α-ethynylestradiol hormone with Langmuir monolayers: The role of charged headgroups". Colloids and Surfaces B: Biointerfaces 158 (жовтень 2017): 627–33. http://dx.doi.org/10.1016/j.colsurfb.2017.07.034.

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6

Zhou, Ze-wei, Wei-sheng Tang, Xiu Shen, Ying Han, Xiao-xue Wang та Liang-an Zhang. "Anti-tumor activities of novel estrogen compound 17a α-D-homo-ethynylestradiol-3-acetate". Chinese Journal of Cancer Research 20, № 1 (2008): 17–20. http://dx.doi.org/10.1007/s11670-008-0017-0.

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7

Shi, Yingying, Lijun Luo, Yefei Zhang та ін. "Synthesis and characterization of α/β-Bi2O3 with enhanced photocatalytic activity for 17α-ethynylestradiol". Ceramics International 43, № 10 (2017): 7627–35. http://dx.doi.org/10.1016/j.ceramint.2017.03.057.

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8

Ruiz, Gilia Cristine Marques, Luis Fernando do Carmo Morato, Wallance Moreira Pazin та ін. "Chemical and morphological effects of the contraceptive hormone 17 α-ethynylestradiol on fluid lipid membranes". Colloids and Surfaces B: Biointerfaces 204 (серпень 2021): 111794. http://dx.doi.org/10.1016/j.colsurfb.2021.111794.

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9

Shi, Yingying, Lijun Luo, Yefei Zhang та ін. "Synthesis and characterization of porous platelet-shaped α-Bi2O3 with enhanced photocatalytic activity for 17α-ethynylestradiol". Journal of Materials Science 53, № 2 (2017): 1049–64. http://dx.doi.org/10.1007/s10853-017-1553-0.

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10

Blewett, Tamzin A., Tiffany L. Chow, Deborah L. MacLatchy та Chris M. Wood. "A species comparison of 17-α-ethynylestradiol uptake and tissue-specific distribution in six teleost fish". Comparative Biochemistry and Physiology Part C: Toxicology & Pharmacology 161 (квітень 2014): 33–40. http://dx.doi.org/10.1016/j.cbpc.2014.01.004.

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11

Ruiz, María Laura, Juan Pablo Rigalli, Agostina Arias та ін. "Estrogen receptor-α mediates human multidrug resistance associated protein 3 induction by 17α-ethynylestradiol. Role of activator protein-1". Biochemical Pharmacology 86, № 3 (2013): 401–9. http://dx.doi.org/10.1016/j.bcp.2013.05.025.

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12

Top, Siden, Michèle Gunn, Gérard Jaouen, Jacqueline Vaissermann, Jean-Claude Daran та John R. Thornback. "Reactions of eq,eq-Re2(CO)8(MeCN)2 with phenylacetylene and α-ethynylestradiol. A new synthesis of acetylide complexes". Journal of Organometallic Chemistry 414, № 1 (1991): C22—C27. http://dx.doi.org/10.1016/0022-328x(91)83255-3.

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13

González, Hernán E., Eliseo A. Eugenín, Gladys Garcés, et al. "Regulation of hepatic connexins in cholestasis: possible involvement of Kupffer cells and inflammatory mediators." American Journal of Physiology-Gastrointestinal and Liver Physiology 282, no. 6 (2002): G991—G1001. http://dx.doi.org/10.1152/ajpgi.00298.2001.

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Abstract:
Hepatocyte gap junction proteins, connexins (Cxs) 26 and 32, are downregulated during obstructive cholestasis (OC) and lipopolysaccharide hepatocellular cholestasis (LPS-HC). We investigated rat hepatic Cxs during ethynylestradiol hepatocellular cholestasis (EE-HC) and choledochocaval fistula (CCF) and compared them with OC and LPS-HC. Levels (immunoblotting) and cellular distribution (immunofluorescence) of Cx26, -32, and -43, as well as macrophage infiltration, were studied in livers of rats under each condition. Cx26 and -32 were reduced in LPS-HC, OC, and CCF. However, in EE-HC, Cx26 did n
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14

Kent, Ute M., Hsia-lien Lin, Danielle E. Mills, Kelly A. Regal та Paul F. Hollenberg. "Identification of 17-α-Ethynylestradiol-Modified Active Site Peptides and Glutathione Conjugates Formed during Metabolism and Inactivation of P450s 2B1 and 2B6". Chemical Research in Toxicology 19, № 2 (2006): 279–87. http://dx.doi.org/10.1021/tx050256o.

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15

Kent, Ute M., Chitra Sridar, Greg Spahlinger та Paul F. Hollenberg. "Modification of Serine 360 by a Reactive Intermediate of 17-α-Ethynylestradiol Results in Mechanism-Based Inactivation of Cytochrome P450s 2B1 and 2B6". Chemical Research in Toxicology 21, № 10 (2008): 1956–63. http://dx.doi.org/10.1021/tx800138v.

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16

Blewett, Tamzin, Deborah L. MacLatchy та Chris M. Wood. "The effects of temperature and salinity on 17-α-ethynylestradiol uptake and its relationship to oxygen consumption in the model euryhaline teleost (Fundulus heteroclitus)". Aquatic Toxicology 127 (лютий 2013): 61–71. http://dx.doi.org/10.1016/j.aquatox.2012.04.009.

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17

Kent, Ute M., Danielle E. Mills, Rajendram V. Rajnarayanan, William L. Alworth та Paul F. Hollenberg. "Effect of 17-α-Ethynylestradiol on Activities of Cytochrome P450 2B (P450 2B) Enzymes: Characterization of Inactivation of P450s 2B1 and 2B6 and Identification of Metabolites". Journal of Pharmacology and Experimental Therapeutics 300, № 2 (2002): 549–58. http://dx.doi.org/10.1124/jpet.300.2.549.

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18

Goto, Takashi, та Juro Hiromi. "Toxicity of 17 α -ethynylestradiol and norethindrone, constituents of an oral contraceptive pill to the swimming and reproduction of cladoceran Daphnia magna , with special reference to their synergetic effect". Marine Pollution Bulletin 47, № 1-6 (2003): 139–42. http://dx.doi.org/10.1016/s0025-326x(03)00052-3.

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19

Holmes, E. L., S. P. Hoile, K. A. Lillycrop та G. C. Burdge. "17-α-ethynylestradiol alters conversion of α-linolenic acid to longer chain PUFA in rat hepatocarcinoma cells". Proceedings of the Nutrition Society 70, OCE4 (2011). http://dx.doi.org/10.1017/s0029665111002850.

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