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Merck
CN

E3625

Sigma-Aldrich

16-Epiestriol

≥93% (HPLC), estradiol metbolite, powder

Synonym(s):

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

Empirical Formula (Hill Notation):
C18H24O3
CAS Number:
547-81-9
Molecular Weight:
288.38
EC Number:
208-937-9
MDL number:
MFCD00067609
UNSPSC Code:
12352202
PubChem Substance ID:
24894522
NACRES:
NA.77

Key Documents

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Product Name

16-Epiestriol, ≥93% (HPLC)

Quality Level

200

Assay

≥93% (HPLC)

form

powder

solubility

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

shipped in

ambient

storage temp.

room temp

SMILES string

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

InChI key

PROQIPRRNZUXQM-UHFFFAOYSA-N

Related Categories

Biochem/physiol Actions

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.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

涉药品监管产品
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Certificates of Analysis (COA)

Lot/Batch Number
0000419128
0000419128
0000395817
0000321141
0000321141

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Sinosh Skariyachan et al.
Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases, 82, 104314-104314 (2020-04-09)
The current study aimed to identify putative drug targets of multidrug resistant Acinetobacter baumannii (MDRAb) and study the therapeutic potential of natural epiestriol-16 by computer aided virtual screening and in vitro studies. The clinical isolates (n = 5) showed extreme dug resistance
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
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
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
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