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QuickView for Estriol (compound)


PubChem
Name: Estriol
PubChem Compound ID: 102232
Description: A hydroxylated metabolite of ESTRADIOL or ESTRONE that has a hydroxyl group at C3-beta, 16-alpha, and 17-beta position. Estriol is a major urinary estrogen. During PREGNANCY, large amount of estriol is produced by the PLACENTA. Isomers with inversion of the hydroxyl group or groups are called epiestriol.
Molecular formula: C27H36O6
Molecular weight: 456.571 g/mol
Synonyms:
Estriol (TN); D01986; 2236-31-9; Estriol; Estriol tripropionate; Estriol tripropionate (JAN); EINECS 218-798-6; Estra-1,3,5(10)-triene-3,16alpha,17beta-triol tripropionate
DrugBank
Identification
Name: Estriol
Name (isomeric): DB04573
Drug Type: small molecule
Description: A hydroxylated metabolite of ESTRADIOL or ESTRONE that has a hydroxyl group at C3-beta, 16-alpha, and 17-beta position. Estriol is a major urinary estrogen. During PREGNANCY, large amount of estriol is produced by the PLACENTA. Isomers with inversion of the hydroxyl group or groups are called epiestriol.
Synonyms:
3,16alpha,17beta-Trihydroxy-1,3,5(10)-estratriene; 16alpha-Hydroxyoestradiol; Tridestrin; 16-alpha-Hydroxyestradiol; Oestriol; 3,16-alpha,17-beta-Trihydroxy-delta-1,3,5-estratriene; Estra-1,3,5(10)-triene-3,16,17-triol; 3,16-alpha,17-beta-Oestriol; 16alpha,17beta-Estriol; 16alpha-Hydroxy-17beta-estradiol.
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Brand: Estriel, Deuslon-A
Category: Estrogens
CAS number: 50-27-1
Pharmacology
Indication: Used as a test to determine the general health of an unborn fetus.
Pharmacology: Estriol (also oestriol) is one of the three main estrogens produced by the human body. It is only produced in significant amounts during pregnancy as it is made by the placenta. In pregnant women with multiple sclerosis (MS), estriol reduces the disease's symptoms noticeably, according to researchers at UCLA's Geffen Medical School.
Mechanism of Action:
Estriol levels can be measured to give an indication of the general health of the fetus. DHEA-S is produced by the adrenal cortex of the fetus. This is converted to estriol by the placenta. If levels of "unconjugated estriol" are abnormally low in a pregnant woman, this may indicate a problem with the development of the child. The drug interacts wi...
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Toxicity: ORAL (LD50): Acute: >2000 mg/kg [Rat].
Affected organisms: Humans and other mammals
Interactions
Drug interaction:
RaloxifeneAssociation not recommended
PhenobarbitalThe enzyme inducer, phenobarbital, decreases the effect of the hormone agent, estriol.
PhenytoinThe enzyme inducer, phenytoin, decreases the effect of the hormone agent, estriol.
PrimidoneThe enzyme inducer, primidone, decreases the effect of the hormone agent, estriol.
PrednisoneThe estrogenic agent, estriol, may increase the effect of corticosteroid, prednisone.
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