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E3625

Sigma-Aldrich

16-Epiestriol

≥93% (HPLC)

Sinonimo/i:

1,3,5(10)-Estratriene-3,16β,17β-triol, 16β-Hydroxy-17β-estradiol, 3,16β,17β-Trihydroxy-1,3,5(10)-estratriene

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About This Item

Formula empirica (notazione di Hill):
C18H24O3
Numero CAS:
547-81-9
Peso molecolare:
288.38
Numero CE:
208-937-9
Numero MDL:
MFCD00067609
Codice UNSPSC:
12352202
ID PubChem:
24894522
NACRES:
NA.77

Livello qualitativo

200

Saggio

≥93% (HPLC)

Forma fisica

powder

Solubilità

ethanol: 0.98-1.02 mg/mL, clear, colorless to faintly yellow

Condizioni di spedizione

ambient

Temperatura di conservazione

room temp

Stringa SMILE

CC12CCC3C(CCc4cc(O)ccc34)C1CC(O)C2O

InChI

1S/C18H24O3/c1-18-7-6-13-12-5-3-11(19)8-10(12)2-4-14(13)15(18)9-16(20)17(18)21/h3,5,8,13-17,19-21H,2,4,6-7,9H2,1H3
PROQIPRRNZUXQM-UHFFFAOYSA-N

Azioni biochim/fisiol

16-Epiestriol is found naturally in various animals, plants, and fungal yeast. It potentially inhibits the growth of colistins and carbapenem-resistant A. baumannii
16-Epiestriol, an estradiol metabolite, possesses anti-inflammatory properties but no glycogenic properties.

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Gloves, type N95 (US)

Certificati d'analisi (COA)

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Xia Xu et al.
Genome medicine, 4(4), 31-31 (2012-05-02)
Endogenous estrogens and estrogen metabolites play an important role in the pathogenesis and development of human breast, endometrial, and ovarian cancers. Increasing evidence also supports their involvement in the development of certain lung, colon and prostate cancers. In this study
Roni T Falk et al.
Breast cancer research : BCR, 15(2), R34-R34 (2013-04-24)
Elevated levels of circulating estrogens are linked to breast cancer risk among postmenopausal women but little is known about the importance of estrogen metabolism. A recently developed liquid chromatography tandem mass spectrometry-based method (LC-MS/MS) measuring a panel of 15 estrogen
Cher M Dallal et al.
Medicine and science in sports and exercise, 48(3), 439-448 (2015-10-16)
Physical activity may reduce endogenous estrogens, but few studies have assessed effects on estrogen metabolism and none have evaluated sedentary behavior in relation to estrogen metabolism. We assessed relationships between accelerometer-measured physical activity and sedentary behavior and 15 urinary estrogens
Sally B Coburn et al.
Cancer causes & control : CCC, 30(1), 75-86 (2018-12-07)
The comparability between serum, plasma, and urinary measurements of estrogen metabolites via liquid chromatography-tandem mass spectrometry (LC-MS/MS) has not been largely explored, and it is unclear if urinary LC-MS/MS measurements are suitable surrogates of circulating levels. Serum, plasma (EDTA and
Jodie M Fleming et al.
BMC medicine, 8, 27-27 (2010-05-25)
Breast cancer studies frequently focus on the role of the tumor microenvironment in the promotion of cancer; however, the influence of the normal breast microenvironment on cancer cells remains relatively unknown. To investigate the role of the normal breast microenvironment
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