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- a synthetic form of estrogen used in combination with a progestin in oral contraceptives
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出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2015/04/13 20:49:29」(JST)
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- 1. アンドロゲン過剰症および男性型多毛症治療におけるエストロゲン・プロゲスチン混合避妊剤の使用 use of combination estrogen progestin contraceptives in the treatment of hyperandrogenism and hirsutism
- 2. 透析患者における消化管疾患 gastrointestinal disease in dialysis patients
English Journal
- Determination of steroid sex hormones in real matrices by bar adsorptive microextraction (BAμE).
- Almeida C1, Nogueira JM2.
- Talanta.Talanta.2015 May;136:145-54. doi: 10.1016/j.talanta.2014.11.013. Epub 2014 Nov 15.
- In the present work, the development of a novel analytical approach which combines a miniaturized bar adsorptive microextraction device with a micro-liquid desorption in one single step, followed by high performance liquid chromatography with diode array detection (BAµE-µLD/HPLC-DAD), is proposed
- PMID 25702996
- Occurrence and analysis of endocrine-disrupting compounds in a water supply system.
- Carvalho AR1, Cardoso VV, Rodrigues A, Ferreira E, Benoliel MJ, Duarte EA.
- Environmental monitoring and assessment.Environ Monit Assess.2015 Mar;187(3):139. doi: 10.1007/s10661-015-4374-0. Epub 2015 Feb 25.
- This paper presents the study of the occurrence of 10 endocrine-disrupting compounds (EDCs) in 60 water samples using a method for simultaneous quantification and confirmation of the presence of these emerging compounds, using ultra-performance liquid chromatography with electrospray ionization and
- PMID 25712629
- Thermodynamic evaluation of aromatic CH/π interactions and rotational entropy in a molecular rotor.
- Pérez-Estrada S1, Rodríguez-Molina B, Xiao L, Santillan R, Jiménez-Osés G, Houk KN, Garcia-Garibay MA.
- Journal of the American Chemical Society.J Am Chem Soc.2015 Feb 18;137(6):2175-8. doi: 10.1021/ja512053t. Epub 2015 Feb 4.
- A molecular rotor built with a stator formed by two rigid 9β-mestranol units having a 90° bent angle linked to a central phenylene rotator has an ideal structure to examine aromatic CH/π interactions. Energies and populations of the multiple solution conformations from quantum-mechanical calculat
- PMID 25635355
Japanese Journal
- Microbial Transformation of Mestranol by Cunninghamella elegans
- CHOUDHARY Muhammad Iqbal,MUSHARRAF Syed Ghulam,SIDDIQUI Zafar Ali,KHAN Naik Tameen,ALI Rahat Azhar,RAHMAN ATTA UR
- Chemical & pharmaceutical bulletin 53(8), 1011-1013, 2005-08-01
- … The microbial transformation of an oral contraceptive, mestranol (1) by Cunninghamella elegans yielded two hydroxylated metabolites, 6β-hydroxymestranol (2) and 6β, 12β-dihydroxymestranol (3). …
- NAID 110003665712
- Relationship between Estrogen Receptor-Binding and Estrogenic Activities of Environmental Estrogens and Suppression by Flavonoids(Biochemistry & Molecular Biology)
- HAN Dal-Ho,DENISON Michael S.,TACHIBANA Hirofumi,YAMADA Koji
- Bioscience, biotechnology, and biochemistry 66(7), 1479-1487, 2002-07-23
- … In the binding assay, pharmaceuticals had a stronger binding activity to hERβ than that of some phytoestrogens (coumestrol, daidzein, genistein, luteolin, chrysin, flavone, and naringenin) or industrial chemicals, but phytoestrogens such as coumestrol had a binding activity as strong as pharmaceuticals such as 17α-ethynylestradiol (EE), tamoxifen (Tam), and mestranol. …
- NAID 110002693851
Related Links
- Origin of mestranol m(ethyl) + estra(trie)n(e), one of its constituents (estra-, estrogenic hormone; see estradiol + tri– + –ene) + –ol 1.
- mes·tra·nol noun \ ˈ mes-trə-ˌ n o l, - ˌ nōl\ Definition of MESTRANOL: a synthetic estrogen C 21 H 26 O 2 used in oral contraceptives Origin of MESTRANOL meth- + estrogen + pregnane (C 21 H 36) + 1-ol First Known Use: 1962
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