D3253
烯雌酚
别名:
3,4-双(4-羟苯基)-2,4-己二烯
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关于此项目
经验公式（希尔记法）:
C18H18O2
化学文摘社编号:
分子量:
266.33
EC Number:
201-519-7
UNSPSC Code:
41116107
PubChem Substance ID:
Beilstein/REAXYS Number:
2053694
MDL number:
InChI key
NFDFQCUYFHCNBW-SCGPFSFSSA-N
InChI
1S/C18H18O2/c1-3-17(13-5-9-15(19)10-6-13)18(4-2)14-7-11-16(20)12-8-14/h3-12,19-20H,1-2H3/b17-3+,18-4+
SMILES string
C\C=C(c1ccc(O)cc1)\C(=C\C)c2ccc(O)cc2
technique(s)
HPLC: suitable, gas chromatography (GC): suitable
application(s)
forensics and toxicology
veterinary
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Biochem/physiol Actions
与己烯雌酚密切相关的合成雌激素化合物
signalword
Danger
hcodes
Hazard Classifications
Carc. 1B - Repr. 2
存储类别
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 3
ppe
Eyeshields, Gloves, type P3 (EN 143) respirator cartridges
法规信息
新产品
此项目有
K Chae et al.
Steroids, 63(3), 149-157 (1998-04-29)
Diethylstilbestrol (DES) is a well-characterized carcinogen in humans and animals although its mechanisms of carcinogenicity are not yet known. While the estrogenic activity of DES is important, there is evidence that oxidative metabolism also plays an important role for its
E G Silva et al.
Gynecologic oncology, 71(2), 240-246 (1998-11-25)
We have been searching for an animal model for ovarian epithelial neoplasms. Our previous study suggested that by giving intermediate doses of testosterone to guinea pigs it is possible to induce cystadenomas in the ovaries in 6 to 10 months.
G G Kuiper et al.
Endocrinology, 138(3), 863-870 (1997-03-01)
The rat estrogen receptor (ER) exists as two subtypes, ER alpha and ER beta, which differ in the C-terminal ligand binding domain and in the N-terminal transactivation domain. In this study we investigated the messenger RNA expression of both ER
Bárbara Socas-Rodríguez et al.
Analytical and bioanalytical chemistry, 409(18), 4467-4477 (2017-06-07)
Within this study, a new method enabling monitoring of various estrogenic substances potentially occurring in milk and dairy products was proposed. Groups of compounds fairly differing in physico-chemical properties and biological activity were analyzed: four natural estrogens, four synthetic estrogens
Bárbara Socas-Rodríguez et al.
Journal of chromatography. A, 1496, 58-67 (2017-04-02)
In this work, a simple and fast methodology has been validated and applied for the analysis of a group of 22 estrogenic compounds including eight phytoestrogens (i.e. daidzein, enterodiol, glycitein, enterolactone, genistein, formononetin, prunetin, biochanin A), six mycotoxins (β-zearalanol, β-zearalenol
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