E3625
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:
Molecular Weight:
288.38
NACRES:
NA.77
PubChem Substance ID:
UNSPSC Code:
12352202
EC Number:
208-937-9
MDL number:
Product Name
16-Epiestriol, ≥93% (HPLC)
Quality Level
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
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
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Regulatory Information
涉药品监管产品
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Concentration of endogenous estrogens and estrogen metabolites in the NCI-60 human tumor cell lines.
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
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
Global Trade Item Number
| SKU | GTIN |
|---|---|
| E3625-100MG | 04061835506293 |