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Merck

E7887

Sigma-Aldrich

17α-Ethynylestradiol 3-cyclopentyl ether

Synonym(e):

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

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About This Item

Empirische Formel (Hill-System):
C25H32O2
CAS-Nummer:
Molekulargewicht:
364.52
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352202
PubChem Substanz-ID:
NACRES:
NA.77

Form

solid

Qualitätsniveau

Versandbedingung

ambient

Lagertemp.

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

InChIKey

PWZUUYSISTUNDW-VAFBSOEGSA-N

Angaben zum Gen

Piktogramme

Health hazardExclamation mark

Signalwort

Danger

Gefahreneinstufungen

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

Lagerklassenschlüssel

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

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Gloves, type P3 (EN 143) respirator cartridges


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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
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
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
Dawei Wang et al.
Physiology & behavior, 104(5), 1024-1030 (2011-07-19)
The theoretical, ecological, physiological, and mathematical aspects of fertility control in mammals have already been well studied, but little attention has been given to the behavioral effects, especially in rodents. We investigated the effects of quinestrol, a synthetic estradiol analog
Xiaohui Lv et al.
Theriogenology, 77(6), 1223-1231 (2012-01-31)
Quinestrol, a synthetic estrogen with marked estrogenic effects and prolonged activity, has potential as a contraceptive for Mongolian gerbils. The objective of this study was to describe the effects of quinestrol on reproductive hormone expression, secretion, and receptor levels in

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