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Oestriol cyclopentyl ether. 1966

F Vischi

UI MeSH Term Description Entries
D004964 Estriol A hydroxylated metabolite of ESTRADIOL or ESTRONE that has a hydroxyl group at C3, 16-alpha, and 17-beta position. Estriol is a major urinary estrogen. During PREGNANCY, a large amount of estriol is produced by the PLACENTA. Isomers with inversion of the hydroxyl group or groups are called epiestriol. (16alpha,17beta)-Estra-1,3,5(10)-Triene-3,16,17-Triol,(16beta,17beta)-Estra-1,3,5(10)-Triene-3,16,17-Triol,16-alpha-Hydroxy-Estradiol,16alpha,17beta-Estriol,16beta-Hydroxy-Estradiol,Epiestriol,Estra-1,3,5(10)-Triene-3,16beta,17beta-Triol,Ovestin,16 alpha Hydroxy Estradiol,16alpha,17beta Estriol,16beta Hydroxy Estradiol
D005260 Female Females
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D014626 Vaginal Smears Collection of pooled secretions of the posterior vaginal fornix for cytologic examination. Cervical Smears,Cervical Smear,Smear, Cervical,Smear, Vaginal,Smears, Cervical,Smears, Vaginal,Vaginal Smear

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[Mutagenicity of bis(2,3-epoxy-cyclopentyl) ether].
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GLC determination of 17 alpha-ethynylestriol 3-cyclopentyl ether.
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Metabolism of doubly labelled ethynylestradiol-3-cyclopentyl ether in women.
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The toxicological assessment of cyclopentyl methyl ether (CPME) as a green solvent.
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[The cyclopentyl ether of 17alpha-ethinyl estradiol in the inhibition of lactation].
May 1963, Rivista d'ostetricia e ginecologia pratica,
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2-Methyltetrahydrofuran and cyclopentyl methyl ether for green solid-phase peptide synthesis.
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[BIOLOGICAL AND CLINICAL EFFECTS OF THE CYCLOPENTYL ENOL ETHER OF 17 ALPHA-ACETOXYPROGESTERONE].
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[EFFECT OF CYCLOPENTYL-ENOL-ETHER OF 17-ALPHA-ACETOXYPROGESTERONE ON THE HUMAN ENDOMETRIUM].
January 1964, Gynaecologia. International monthly review of obstetrics and gynecology. Revue internationale mensuelle d'obstetrique et de gynecologie. Monatsschrift fur Geburtshilfe und Gynakologie,
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Cyclopentyl methyl ether: an alternative solvent for palladium-catalyzed direct arylation of heteroaromatics.
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Prolonged oestrogenic activity in rats after single oral administration of ethinyloestradiol-3-cyclopentyl ether.
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