BGC > Product Search > Estrone

Molecular Formula: C18H22O2
Molecular Weight: 270.37

Molecular Formula: C18H22O2
Molecular Weight: 270.37

Molecular Formula: C18H22O2
Molecular Weight: 270.37

EINECS :200-164-5
Molecular formula :C18H22O2

EINECS :200-164-5
Molecular formula :C18H22O2

EINECS :200-164-5
Molecular formula :C18H22O2

EINECS :200-164-5
Molecular formula :C18H22O2

EINECS :200-164-5
Molecular formula :C18H22O2

EINECS :200-164-5
Molecular formula :C18H22O2

Description :
Estrone is one of the three naturally occurring estrogens, the others being estradiol and estriol. Estrone is synthesized from androstenedione by the aromatase enzyme system in the ovaries and placenta, and is also synthesized from estradiol by 17-hydroxy steroid dehydrogenase in the liver. Serum concentrations of estrone in premenopausal women fluctuate according to the menstral cycle and becomes the most predominant estrogen in postmenopausal women. The binding affinities of estrone to the estrogen receptors α and β are approximately 60% and 37% relative to estradiol.

• Molecular Weight :270.372
• Boiling Point :445.2±45.0 °C at 760 mmHg
• Melting Point :258-260 °C
• Purity :0.95

Molecular Formula :
C18H22O2
Canonical SMILES :
CC12CCC3C(C1CCC2=O)CCC4=C3C=CC(=C4)O
InChI :
InChI=1S/C18H22O2/c1-18-9-8-14-13-5-3-12(19)10-11(13)2-4-15(14)16(18)6-7-17(18)20/h3,5,10,14-16,19H,2,4,6-9H2,1H3/t14-,15-,16+,18+/m1/s1
InChIKey :
DNXHEGUUPJUMQT-CBZIJGRNSA-N
Solubility :
0.03 g/L
Appearance :
White crystalline powder
Synonyms :
3-Hydroxyestra-1,3,5(10)-trien-17-one; (+)-Estrone; 1,3,5(10)-Estratrien-3-ol-17-one; 3-Hydroxy-17-keto-estra-1,3,5-triene; Aquacrine; Crinovaryl; Cristallovar; Crystogen; WAY 164397; Wynestron;

More details are to be found here

Description :
Estrone is one of the three naturally occurring estrogens, the others being estradiol and estriol. Estrone is synthesized from androstenedione by the aromatase enzyme system in the ovaries and placenta, and is also synthesized from estradiol by 17-hydroxy steroid dehydrogenase in the liver. Serum concentrations of estrone in premenopausal women fluctuate according to the menstral cycle and becomes the most predominant estrogen in postmenopausal women. The binding affinities of estrone to the estrogen receptors α and β are approximately 60% and 37% relative to estradiol.

• Molecular Weight :270.372
• Boiling Point :445.2±45.0 °C at 760 mmHg
• Melting Point :258-260 °C
• Purity :0.95

Molecular Formula :
C18H22O2
Canonical SMILES :
CC12CCC3C(C1CCC2=O)CCC4=C3C=CC(=C4)O
InChI :
InChI=1S/C18H22O2/c1-18-9-8-14-13-5-3-12(19)10-11(13)2-4-15(14)16(18)6-7-17(18)20/h3,5,10,14-16,19H,2,4,6-9H2,1H3/t14-,15-,16+,18+/m1/s1
InChIKey :
DNXHEGUUPJUMQT-CBZIJGRNSA-N
Solubility :
0.03 g/L
Appearance :
White crystalline powder
Synonyms :
3-Hydroxyestra-1,3,5(10)-trien-17-one; (+)-Estrone; 1,3,5(10)-Estratrien-3-ol-17-one; 3-Hydroxy-17-keto-estra-1,3,5-triene; Aquacrine; Crinovaryl; Cristallovar; Crystogen; WAY 164397; Wynestron;

More details are to be found here

Description :
Estrone is one of the three naturally occurring estrogens, the others being estradiol and estriol. Estrone is synthesized from androstenedione by the aromatase enzyme system in the ovaries and placenta, and is also synthesized from estradiol by 17-hydroxy steroid dehydrogenase in the liver. Serum concentrations of estrone in premenopausal women fluctuate according to the menstral cycle and becomes the most predominant estrogen in postmenopausal women. The binding affinities of estrone to the estrogen receptors α and β are approximately 60% and 37% relative to estradiol.

• Molecular Weight :270.372
• Boiling Point :445.2±45.0 °C at 760 mmHg
• Melting Point :258-260 °C
• Purity :0.95

Molecular Formula :
C18H22O2
Canonical SMILES :
CC12CCC3C(C1CCC2=O)CCC4=C3C=CC(=C4)O
InChI :
InChI=1S/C18H22O2/c1-18-9-8-14-13-5-3-12(19)10-11(13)2-4-15(14)16(18)6-7-17(18)20/h3,5,10,14-16,19H,2,4,6-9H2,1H3/t14-,15-,16+,18+/m1/s1
InChIKey :
DNXHEGUUPJUMQT-CBZIJGRNSA-N
Solubility :
0.03 g/L
Appearance :
White crystalline powder
Synonyms :
3-Hydroxyestra-1,3,5(10)-trien-17-one; (+)-Estrone; 1,3,5(10)-Estratrien-3-ol-17-one; 3-Hydroxy-17-keto-estra-1,3,5-triene; Aquacrine; Crinovaryl; Cristallovar; Crystogen; WAY 164397; Wynestron;

More details are to be found here

Description :
Estrone is one of the three naturally occurring estrogens, the others being estradiol and estriol. Estrone is synthesized from androstenedione by the aromatase enzyme system in the ovaries and placenta, and is also synthesized from estradiol by 17-hydroxy steroid dehydrogenase in the liver. Serum concentrations of estrone in premenopausal women fluctuate according to the menstral cycle and becomes the most predominant estrogen in postmenopausal women. The binding affinities of estrone to the estrogen receptors α and β are approximately 60% and 37% relative to estradiol.

• Molecular Weight :270.372
• Boiling Point :445.2±45.0 °C at 760 mmHg
• Melting Point :258-260 °C
• Purity :0.95

Molecular Formula :
C18H22O2
Canonical SMILES :
CC12CCC3C(C1CCC2=O)CCC4=C3C=CC(=C4)O
InChI :
InChI=1S/C18H22O2/c1-18-9-8-14-13-5-3-12(19)10-11(13)2-4-15(14)16(18)6-7-17(18)20/h3,5,10,14-16,19H,2,4,6-9H2,1H3/t14-,15-,16+,18+/m1/s1
InChIKey :
DNXHEGUUPJUMQT-CBZIJGRNSA-N
Solubility :
0.03 g/L
Appearance :
White crystalline powder
Synonyms :
3-Hydroxyestra-1,3,5(10)-trien-17-one; (+)-Estrone; 1,3,5(10)-Estratrien-3-ol-17-one; 3-Hydroxy-17-keto-estra-1,3,5-triene; Aquacrine; Crinovaryl; Cristallovar; Crystogen; WAY 164397; Wynestron;

More details are to be found here

Description :
Estrone is one of the three naturally occurring estrogens, the others being estradiol and estriol. Estrone is synthesized from androstenedione by the aromatase enzyme system in the ovaries and placenta, and is also synthesized from estradiol by 17-hydroxy steroid dehydrogenase in the liver. Serum concentrations of estrone in premenopausal women fluctuate according to the menstral cycle and becomes the most predominant estrogen in postmenopausal women. The binding affinities of estrone to the estrogen receptors α and β are approximately 60% and 37% relative to estradiol.

• Molecular Weight :270.372
• Boiling Point :445.2±45.0 °C at 760 mmHg
• Melting Point :258-260 °C
• Purity :0.95

Molecular Formula :
C18H22O2
Canonical SMILES :
CC12CCC3C(C1CCC2=O)CCC4=C3C=CC(=C4)O
InChI :
InChI=1S/C18H22O2/c1-18-9-8-14-13-5-3-12(19)10-11(13)2-4-15(14)16(18)6-7-17(18)20/h3,5,10,14-16,19H,2,4,6-9H2,1H3/t14-,15-,16+,18+/m1/s1
InChIKey :
DNXHEGUUPJUMQT-CBZIJGRNSA-N
Solubility :
0.03 g/L
Appearance :
White crystalline powder
Synonyms :
3-Hydroxyestra-1,3,5(10)-trien-17-one; (+)-Estrone; 1,3,5(10)-Estratrien-3-ol-17-one; 3-Hydroxy-17-keto-estra-1,3,5-triene; Aquacrine; Crinovaryl; Cristallovar; Crystogen; WAY 164397; Wynestron;

More details are to be found here

Description :
Estrone is one of the three naturally occurring estrogens, the others being estradiol and estriol. Estrone is synthesized from androstenedione by the aromatase enzyme system in the ovaries and placenta, and is also synthesized from estradiol by 17-hydroxy steroid dehydrogenase in the liver. Serum concentrations of estrone in premenopausal women fluctuate according to the menstral cycle and becomes the most predominant estrogen in postmenopausal women. The binding affinities of estrone to the estrogen receptors α and β are approximately 60% and 37% relative to estradiol.

• Molecular Weight :270.372
• Boiling Point :445.2±45.0 °C at 760 mmHg
• Melting Point :258-260 °C
• Purity :0.95

Molecular Formula :
C18H22O2
Canonical SMILES :
CC12CCC3C(C1CCC2=O)CCC4=C3C=CC(=C4)O
InChI :
InChI=1S/C18H22O2/c1-18-9-8-14-13-5-3-12(19)10-11(13)2-4-15(14)16(18)6-7-17(18)20/h3,5,10,14-16,19H,2,4,6-9H2,1H3/t14-,15-,16+,18+/m1/s1
InChIKey :
DNXHEGUUPJUMQT-CBZIJGRNSA-N
Solubility :
0.03 g/L
Appearance :
White crystalline powder
Synonyms :
3-Hydroxyestra-1,3,5(10)-trien-17-one; (+)-Estrone; 1,3,5(10)-Estratrien-3-ol-17-one; 3-Hydroxy-17-keto-estra-1,3,5-triene; Aquacrine; Crinovaryl; Cristallovar; Crystogen; WAY 164397; Wynestron;

More details are to be found here

Description :
Estrone is one of the three naturally occurring estrogens, the others being estradiol and estriol. Estrone is synthesized from androstenedione by the aromatase enzyme system in the ovaries and placenta, and is also synthesized from estradiol by 17-hydroxy steroid dehydrogenase in the liver. Serum concentrations of estrone in premenopausal women fluctuate according to the menstral cycle and becomes the most predominant estrogen in postmenopausal women. The binding affinities of estrone to the estrogen receptors α and β are approximately 60% and 37% relative to estradiol.

• Molecular Weight :270.372
• Boiling Point :445.2±45.0 °C at 760 mmHg
• Melting Point :258-260 °C
• Purity :0.95

Molecular Formula :
C18H22O2
Canonical SMILES :
CC12CCC3C(C1CCC2=O)CCC4=C3C=CC(=C4)O
InChI :
InChI=1S/C18H22O2/c1-18-9-8-14-13-5-3-12(19)10-11(13)2-4-15(14)16(18)6-7-17(18)20/h3,5,10,14-16,19H,2,4,6-9H2,1H3/t14-,15-,16+,18+/m1/s1
InChIKey :
DNXHEGUUPJUMQT-CBZIJGRNSA-N
Solubility :
0.03 g/L
Appearance :
White crystalline powder
Synonyms :
3-Hydroxyestra-1,3,5(10)-trien-17-one; (+)-Estrone; 1,3,5(10)-Estratrien-3-ol-17-one; 3-Hydroxy-17-keto-estra-1,3,5-triene; Aquacrine; Crinovaryl; Cristallovar; Crystogen; WAY 164397; Wynestron;

More details are to be found here

Description :
Estrone is one of the three naturally occurring estrogens, the others being estradiol and estriol. Estrone is synthesized from androstenedione by the aromatase enzyme system in the ovaries and placenta, and is also synthesized from estradiol by 17-hydroxy steroid dehydrogenase in the liver. Serum concentrations of estrone in premenopausal women fluctuate according to the menstral cycle and becomes the most predominant estrogen in postmenopausal women. The binding affinities of estrone to the estrogen receptors α and β are approximately 60% and 37% relative to estradiol.

• Molecular Weight :270.372
• Boiling Point :445.2±45.0 °C at 760 mmHg
• Melting Point :258-260 °C
• Purity :0.95

Molecular Formula :
C18H22O2
Canonical SMILES :
CC12CCC3C(C1CCC2=O)CCC4=C3C=CC(=C4)O
InChI :
InChI=1S/C18H22O2/c1-18-9-8-14-13-5-3-12(19)10-11(13)2-4-15(14)16(18)6-7-17(18)20/h3,5,10,14-16,19H,2,4,6-9H2,1H3/t14-,15-,16+,18+/m1/s1
InChIKey :
DNXHEGUUPJUMQT-CBZIJGRNSA-N
Solubility :
0.03 g/L
Appearance :
White crystalline powder
Synonyms :
3-Hydroxyestra-1,3,5(10)-trien-17-one; (+)-Estrone; 1,3,5(10)-Estratrien-3-ol-17-one; 3-Hydroxy-17-keto-estra-1,3,5-triene; Aquacrine; Crinovaryl; Cristallovar; Crystogen; WAY 164397; Wynestron;

More details are to be found here

Description :
Estrone is one of the three naturally occurring estrogens, the others being estradiol and estriol. Estrone is synthesized from androstenedione by the aromatase enzyme system in the ovaries and placenta, and is also synthesized from estradiol by 17-hydroxy steroid dehydrogenase in the liver. Serum concentrations of estrone in premenopausal women fluctuate according to the menstral cycle and becomes the most predominant estrogen in postmenopausal women. The binding affinities of estrone to the estrogen receptors α and β are approximately 60% and 37% relative to estradiol.

• Molecular Weight :270.372
• Boiling Point :445.2±45.0 °C at 760 mmHg
• Melting Point :258-260 °C
• Purity :0.95

Molecular Formula :
C18H22O2
Canonical SMILES :
CC12CCC3C(C1CCC2=O)CCC4=C3C=CC(=C4)O
InChI :
InChI=1S/C18H22O2/c1-18-9-8-14-13-5-3-12(19)10-11(13)2-4-15(14)16(18)6-7-17(18)20/h3,5,10,14-16,19H,2,4,6-9H2,1H3/t14-,15-,16+,18+/m1/s1
InChIKey :
DNXHEGUUPJUMQT-CBZIJGRNSA-N
Solubility :
0.03 g/L
Appearance :
White crystalline powder
Synonyms :
3-Hydroxyestra-1,3,5(10)-trien-17-one; (+)-Estrone; 1,3,5(10)-Estratrien-3-ol-17-one; 3-Hydroxy-17-keto-estra-1,3,5-triene; Aquacrine; Crinovaryl; Cristallovar; Crystogen; WAY 164397; Wynestron;

More details are to be found here