estrone


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es·trone

 (ĕs′trōn′)
n.
An estrogenic hormone, C18H22O2, that is secreted by the ovaries and by fatty tissue. It is the main form of estrogen in postmenopausal women.

American Heritage® Dictionary of the English Language, Fifth Edition. Copyright © 2016 by Houghton Mifflin Harcourt Publishing Company. Published by Houghton Mifflin Harcourt Publishing Company. All rights reserved.

estrone

(ˈɛstrəʊn; ˈiːstrəʊn)
n
(Biochemistry) the usual US spelling of oestrone
Collins English Dictionary – Complete and Unabridged, 12th Edition 2014 © HarperCollins Publishers 1991, 1994, 1998, 2000, 2003, 2006, 2007, 2009, 2011, 2014

es•trone

(ˈɛs troʊn)

n.
an estrogenic hormone, C18H22O2, produced by the ovarian follicles and found during pregnancy in urine and placental tissue.
[1930–35; estr(in) an earlier name (estr(us) + -in1) + -one]
Random House Kernerman Webster's College Dictionary, © 2010 K Dictionaries Ltd. Copyright 2005, 1997, 1991 by Random House, Inc. All rights reserved.
ThesaurusAntonymsRelated WordsSynonymsLegend:
Noun1.estrone - a naturally occurring weak estrogenic hormone secreted by the mammalian ovary; synthesized (trade name Estronol) and used to treat estrogen deficiency
estrogen, oestrogen - a general term for female steroid sex hormones that are secreted by the ovary and responsible for typical female sexual characteristics
ketosteroid - a steroid containing a ketone group
Based on WordNet 3.0, Farlex clipart collection. © 2003-2012 Princeton University, Farlex Inc.
Translations

es·trone

n. estrona, hormona estrogénica.
English-Spanish Medical Dictionary © Farlex 2012
References in periodicals archive ?
A study with 24 postmenopausal women found that adding yams to two meals per day could help increase estrone and estradiol in the blood, which may ease menopause symptoms.
The effects of prochloraz on estradiol (D), estriol (E), and estrone (F) production by H295R and BeWo cells in monoculture or coculture (24-h exposure).
Many CC HT prescribers worldwide have mixed estrogens in the form of Bi-Est (estradiol + estrone) or Tri-Est (estradiol + estrone + estriol), which is unnecessary either in terms of hormone metabolism or postmenopausal hormone levels.
It markedly reduces the serum concentrations of estrogen metabolites, namely estrone, estradiol and estronesulphate.
Up until this point in medical practice, only estradiol, estrone and estriol are measured, and not, total estrogen.
[13,14] Estrone is an utmost circulating form of estrogen in postmenopausal state.
The mean concentration of estradiol and estrone remained within average postmenopausal range for both the doses.
MALES FEMALE (Luteal Phase) Hormone (LabCorp) Units Approximate Median Value DHEA-S pg/dL 347,400,000 271,600,000 Total Testosterone pg/dL 590,000 28,000 DHEA pg/dL 366,000 366,000 Pregnenolone pg/dL 100,000 100,000 Progesterone pg/dL 25,000 1,285,000 Total Estrogens pg/dL 7,750 25,300 Estrone (E1) pg/dL 4,200 8,200 Estradiol (E2) pg/dL 2,510 12,740 Free Testosterone pg/dL 1,790 210 As you can see, the level of DHEA-S (the form of DHEA tested in male and female panels) exceeds all the other steroid hormones combined!
Pure standards (>98%) of ketoprofen (KET), ibuprofen (IBU), bezafibrate (BF), triclosan (TCS), triclocarban (TCC), chloramphenicol (CAL), norfloxacin (NOR), ofloxacin (OFL), ciprofloxacin (CIP), acetaminophen (ACE), atenolol (ATE), tetracycline (TCN), diclofenac salt (DIC), estrone (E1), 17[beta]-estradiol (E2), estriol (E3), and 17[alpha]-ethinylestradiol (EE2) were all purchased from Sigma-Aldrich (Aston Manor, South Africa).
This study is the first report that determines the effects of 17[beta]-estradiol, estrone, progesterone and androsterone among the mammalian sex hormones on in vitro regeneration of Triticale mature embryos.
The steroidal thiosemicarbazones 1-4 were obtained by reacting estrone and pregnenolone or their ester with thiosemicarbazide and then the reaction of compounds 1-4 with Cu[Cl.sub.2] x 2[H.sub.2]O gave steroidal copper (Cu (II)) complexes 5-8 as a mixture of (R)- and (S)-configuration isomers, respectively.
As the gene product of CYP19, aromatase can act on androstenedione generated from the adrenal cortex of adipose tissues to form estrone and testos terone in ovarian tissues to produce androstenedione, and then transform a part of androstenedione into estrone.15,16 Theoretically, LE may be superior to CC because it has no peripheral anti-estrogen effect.