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E7887

Sigma-Aldrich

17α-Ethynylestradiol 3-cyclopentyl ether

Synonym(s):

17α-Ethynyl-1,3,5(10)-estratriene-3,17β-diol 3-cyclopentyl ether, Quinestrol

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About This Item

Empirical Formula (Hill Notation):
C25H32O2
CAS Number:
152-43-2
Molecular Weight:
364.52
EC Number:
205-803-1
MDL number:
MFCD00079189
UNSPSC Code:
12352202
PubChem Substance ID:
24894659
NACRES:
NA.77
Pricing and availability is not currently available.

form

solid

Quality Level

200

shipped in

ambient

storage temp.

room temp

SMILES string

[H][C@]12CC[C@@]3(C)[C@@]([H])(CC[C@@]3(O)C#C)[C@]1([H])CCc4cc(OC5CCCC5)ccc24

InChI

1S/C25H32O2/c1-3-25(26)15-13-23-22-10-8-17-16-19(27-18-6-4-5-7-18)9-11-20(17)21(22)12-14-24(23,25)2/h1,9,11,16,18,21-23,26H,4-8,10,12-15H2,2H3/t21-,22-,23+,24+,25+/m1/s1

InChI key

PWZUUYSISTUNDW-VAFBSOEGSA-N

Gene Information

human ... ESR1(2099) , ESR2(2100)

Pictograms

Health hazardExclamation mark
GHS08,GHS07

Signal Word

Danger

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Carc. 1B - Repr. 1B

Storage Class Code

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
089F0245

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Xiao-Hui Lv et al.
Experimental animals, 60(5), 489-496 (2011-11-02)
The contraceptive effects of quinestrol in Mongolian gerbils were examined. The results showed that body weight significantly increased after quinestrol treatment, except in the group that received the highest dose. The gonadosomatic index of ovaries decreased, whereas that of uteri
Wei Shen et al.
Experimental animals, 60(5), 445-453 (2011-11-02)
The hypothesis that quinestrol exerts testicular damage via oxidative stress was investigated in male gerbils using a daily oral gavage of 3.5 mg/kg body weight for 2 weeks (the multidose-treated group) or 35 mg/kg body weight (the single-dose-treated group). The
Tao Tang et al.
Chemosphere, 89(11), 1419-1425 (2012-07-10)
Quinestrol is synthetic estrogen used in contraceptive and hormone replacement therapy and occasionally for treating breast cancer and prostate cancer. It can make its way into the environment through sewage discharge and waste disposal produced by human excretions. In this
Xiaohui Lv et al.
Reproductive biology, 12(3), 285-292 (2012-11-17)
The effects of the two sterilants, quinestrol (QE) and levonorgestrel (LNG) on serum prolactin (PRL) level in lactating Mongolian gerbils and reproductive parameters of their offspring were examined in the study. Both sterilants increased the serum PRL level in lactating
Xiaohui Lv et al.
Zoological science, 29(1), 37-42 (2012-01-12)
The effects of treatment with a combination of levonorgestrel and quinestrol (EP-1; ratio of 2:1) on reproductive hormone levels and the expression of their receptors in female Mongolian gerbils were examined. We show that serum follicle-stimulating hormone (FSH) and luteinizing
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