Thermo Scientific Chemicals

Estrone, 99+%, Thermo Scientific Chemicals

Catalog number: 117840250
25 g, Glass bottle, Each
Thermo Scientific Chemicals

Estrone, 99+%, Thermo Scientific Chemicals

Catalog number: 117840250
25 g, Glass bottle, Each
Quantity
Packaging

Chemical Identifiers

CAS
53-16-7
IUPAC Name
(3aS,3bR,9bS,11aS)-7-hydroxy-11a-methyl-1H,2H,3H,3aH,3bH,4H,5H,9bH,10H,11H,11aH-cyclopenta[a]phenanthren-1-one
Molecular Formula
C18H22O2
InChI Key
DNXHEGUUPJUMQT-CBZIJGRNSA-N
SMILES
C[C@]12CC[C@H]3[C@@H](CCC4=CC(O)=CC=C34)[C@@H]1CCC2=O
Appearance (Color)
White to almost white
Infrared spectrum
Conforms
HPLC
>=99.0 % (on dried substance)
Additional info
limit of equilenin and equilin: passes test
Appearance (Form)
Powder or crystals

Description

This Thermo Scientific Chemicals brand product was originally part of the Acros Organics product portfolio. Some documentation and label information may refer to the legacy brand. The original Acros Organics product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

General Description

• Estrone is an aromatized C18 steroid considered one of the major mammalian estrogen and a sex hormone. It shows antineoplastic and bone density conservative activities.

• This compound can interact with estrogen receptors in target tissues to produce similar effects to estradiol. Hormone-bound estrogen receptors dimerize, translocate to the nucleus of cells and bind to estrogen response elements (ERE) of genes. Binding to ERE alters the transcription rate of affected genes.

Applications

• Estrone has the ability to increase the hepatic synthesis of sex hormone binding globulin (SHBG), thyroid-binding globulin (TBG), and other serum proteins.

• It can suppress the release of follicle-stimulating hormone and luteinizing hormone.

• This compound can be produced from androstenedione or testosterone via estradiol. In vivo, it can be generated mainly in the ovaries, placenta, and peripheral tissues (especially adipose tissue) through conversion of androstenedione. It may be metabolized to 16-α-hydroxyestrone, which may be reduced to estriol by estradiol dehydrogenase.

• It has been used as medium supplement for hormone-based degranulation studies of natural killer cells.

• It is used as medium component for monitoring fatty acid synthase activity in breast adenocarcinoma cell lines.

RUO – Research Use Only

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