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Estrone

Catalog No. DB00655 Name DrugBank
CAS Number 53-16-7 Website http://www.ualberta.ca/
M. F. C18H22O2 Telephone (780) 492-3111
M. W. 270.36608 Fax (780) 492-1071
Purity Email david.wishart@ualberta.ca
Storage Chembase ID: 537

SYNONYMS

IUPAC name
(1S,10R,11S,15S)-5-hydroxy-15-methyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadeca-2(7),3,5-trien-14-one
IUPAC Traditional name
estrone
Brand Name
Cristallovar
GSS 33
Wynestronpencap M
Oestroform
Oestrone
Crystogen
Destrone
Esterone
Estrovarin
Femestrone Inj.
Femidyn
Follidrin
Kestrone
Ketophydroxyestrin
Menagen
Oestrone [Steroidal Oestrogens]
Aquacrine
Endofolliculina
Estrin
Estron
Estrona [Spanish]
Estrone-A
Estronum [INN-Latin]
Estrugenone
Folisan
Follicunodis
Glandubolin
Hormofollin
Hormovarine
Ketodestrin
Ketohydroxyestrin
Ketohydroxyoestrin
Menformon
Menformon A
Penncap M
Solliculin
Thelykinin
Tokokin
Unden
Crinovaryl
Disynformon
Estrogenic Substance
Estrol
Estrona
Estrona [INN-Spanish]
Estrone [Usan:Inn]
Estrusol
Femestrone Injection
Fermidyn
Folikrin
Folipex
Follestrine
Follestrol
Follicular Hormone
Folliculin
Folliculine
Folliculine Benzoate
Hiestrone
Hormestrin
Ketohydroxy-Estratriene
Kolpon
Mestronaq
OVEX
Oestrin
Oestronum
Oestroperos
Ovifollin
Perlatan
Sinafid M-48
Theelin
Thelestrin
Thynestron
Wynestron

DATABASE IDS

PubChem CID 5870
CAS Number 53-16-7
PubChem SID 46505916

PROPERTIES

Hydrophobicity(logP) 3.6
Solubility 3 g/100mL

DETAILS

Description (English)
Item Information
Drug Groups approved
Description Estrone, one of the major mammalian estrogens, is an aromatized C18 steroid with a 3-hydroxyl group and a 17-ketone. It is produced in vivo from androstenedione or from testosterone via estradiol. It is produced primarily in the ovaries, placenta, and in peripheral tissues (especially adipose tissue) through conversion of adrostenedione. Estrone may be further metabolized to 16-alpha-hydroxyestrone, which may be reduced to estriol by estradiol dehydrogenase.
Indication For management of perimenopausal and postmenopausal symptoms.
Pharmacology Estrone, a synthetically prepared or naturally occurring steroidal estrogen obtained from pregnant equine urine, is the primary circulating estrogen after menopause. Estrone is naturally derived from the peripheral conversion of androstenedione by an aromatase enzyme found in adipose tissues and is converted to estradiol in peripheral tissues. The estrogenic potency of estrone is one third that of estradiol. Estropipate is piperazine-stabilized estrone sulfate. Estrone, and estropipate are used to treat abnormalities related to gonadotropin hormone dysfunction, vasomotor symptoms, atrophic vaginitis, and vulvar atrophy associated with menopause, and for the prevention of osteoporosis due to estrogen deficiency.
Toxicity Symptoms of overdose include nausea and vomiting. Estrogen related side effects include nausea, breast tenderness, fluid retention and edema, headaches and/or migraines, chloasma and poor contact lens fit. Estrogen hormone deficiency is associated with breakthrough bleeding, hypomenorrhea, irritability, depression and menopausal symptoms. Withdrawal bleeds may occur in females.
Affected Organisms
Humans and other mammals
Biotransformation Hepatic.
Absorption 43%
Half Life 19 hours
Protein Binding > 95%
References
Miyoshi Y, Tanji Y, Taguchi T, Tamaki Y, Noguchi S: Association of serum estrone levels with estrogen receptor-positive breast cancer risk in postmenopausal Japanese women. Clin Cancer Res. 2003 Jun;9(6):2229-33. [Pubmed]
Kajta M, Lason W, Bien E, Marszal M: Neuroprotective effects of estrone on NMDA-induced toxicity in primary cultures of rat cortical neurons are independent of estrogen receptors. Pol J Pharmacol. 2002 Nov-Dec;54(6):727-9. [Pubmed]
External Links
Wikipedia

REFERENCES

  • Miyoshi Y, Tanji Y, Taguchi T, Tamaki Y, Noguchi S: Association of serum estrone levels with estrogen receptor-positive breast cancer risk in postmenopausal Japanese women. Clin Cancer Res. 2003 Jun;9(6):2229-33. Pubmed
  • Kajta M, Lason W, Bien E, Marszal M: Neuroprotective effects of estrone on NMDA-induced toxicity in primary cultures of rat cortical neurons are independent of estrogen receptors. Pol J Pharmacol. 2002 Nov-Dec;54(6):727-9. Pubmed