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E3750

Sigma-Aldrich

17-Epiestriol

Synonym(e):

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

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About This Item

Empirische Formel (Hill-System):
C18H24O3
CAS-Nummer:
1228-72-4
Molekulargewicht:
288.38
MDL-Nummer:
MFCD00069500
UNSPSC-Code:
12352200
PubChem Substanz-ID:
24894525
NACRES:
NA.77
Form:
powder
Assay:
≥98.00% (TLC)

Sterilität

non-sterile

Qualitätsniveau

200

Assay

≥98.00% (TLC)

Form

powder

Methode(n)

inhibition assay: suitable

Farbe

off-white to yellow

Löslichkeit

chloroform: methanol (1:1): 9.80-10.20 mg/mL, clear, colorless to faintly yellow

Versandbedingung

ambient

Lagertemp.

room temp

SMILES String

CC12CCC3C(CCc4cc(O)ccc34)C1C[C@@H](O)[C@H]2O

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/t13?,14?,15?,16-,17-,18?/m1/s1

InChIKey

PROQIPRRNZUXQM-CKMBUZLOSA-N

Biochem./physiol. Wirkung

17-epiestriol is an estradiol metabolite and a selective estrogen receptor (ER) beta agonist.

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Gloves, type N95 (US)

Hier finden Sie alle aktuellen Versionen:

Analysenzertifikate (COA)

Lot/Batch Number
038M4016V
13160105
126M4165V
075M4078V
086M4102V

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Die Dokumentenbibliothek aufrufen

Carien van der Berg et al.
Analytical biochemistry, 590, 113531-113531 (2019-12-06)
An imbalance in the estrogen metabolism has been associated with an increased risk of breast cancer development. Evaluation of the estrogen biotransformation capacity requires monitoring of various estrogen metabolites. Up to now, only some estrogen metabolites could be measured in
Marcelo O Dietrich et al.
Trends in neurosciences, 36(2), 65-73 (2013-01-16)
The past 20 years witnessed an enormous leap in understanding of the central regulation of whole-body energy metabolism. Genetic tools have enabled identification of the region-specific expression of peripheral metabolic hormone receptors and have identified neuronal circuits that mediate the
Mitsuhiro Ueda et al.
Enzyme and microbial technology, 51(6-7), 402-407 (2012-10-09)
A protein with strong removal activity against the natural estrogen estriol was purified from a culture supernatant of Pleurotus eryngii var. tuoliensis C.J. Mou. The protein was characterized as a laccase and had a molecular mass of 60kDa on SDS-PAGE.
Swastika Surujlal-Naicker et al.
Journal of environmental science and health. Part A, Toxic/hazardous substances & environmental engineering, 48(1), 37-47 (2012-10-04)
Wastewater effluents have been documented as major contributors of hormone endocrine disrupting compounds (EDCs) in to the aquatic ecosystem. The need for rapid, simple and cost effective methods to detect these EDCs has increased. The use of Radio-immunoassays (RIA) were
Maya Frank et al.
Prenatal diagnosis, 33(2), 191-195 (2013-01-08)
To compare the profile of mid gestation triple test serum markers between a cohort of women with history of pregnancy complications with hereditary versus acquired thrombophilia. All were treated with low molecular weight heparin (LMWH) prior to 12 weeks' gestation.
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