CAS 57-63-6
:Éthinylestradiol
- (17Alpha)-17-Ethynylestra-1,3,5(10)-Triene-3,17-Diol
- (17Beta)-17-Ethynylestra-1,3,5(10)-Triene-3,17-Diol
- (17α)-19-Norpregna-1,3,5(10)-trien-20-yne-3,17-diol
- (8Alpha,13Alpha,17Beta)-17-Ethynylestra-1,3,5(10)-Triene-3,17-Diol
- (8Xi,9Xi,14Xi,17Beta)-17-Ethynylestra-1,3,5(10)-Triene-3,17-Diol
- 17-Ethinyl-3,17-estradiol
- 17-Ethinylestradiol
- 17-Ethynyl Estradiol
- 17-Ethynyl-3,17-dihydroxy-1,3,5-oestratriene
- 17-Ethynylestra-1,3,5(10)-Triene-3,17-Diol
- 17-Ethynylestra-1,3,5(10)-triene-3,17β-diol
- 17-Ethynylestradiol
- 17-Nor-17α-pregna-1,3,5-(10)-trien-20-yne-3,17-diol
- 17A-Ethynyl-1,3,5(10)-Estratriene-3,17B-Diol
- 17Alpha-Ethynyl-3,17-Dihydroxy-Delta-(Sup1,3,5)-Estratriene
- 17alpha-Ethynyl-3-hydroxy-1,3,5(10)-estratrien-17beta-ol
- 17α-Ethinyl estradiol (EE2)
- 17α-Ethinyl-1,3,5(10)-estratriene-3,17-diol
- 17α-Ethinyl-17β-estradiol
- 17α-Ethinyl-3,17-dihydroxy-Δ1,3,5-estratriene
- 17α-Ethinyl-3,17-dihydroxy-Δ<sup>1,3,5</sup>-estratriene
- 17α-Ethinylestra-1,3,5(10)-triene-3,17β-diol
- 17α-Ethinylestradiol
- 17α-Ethynylestra-1,3,5(10)-triene-3,17β-diol
- 17α-Ethynylestra-3,17β-diol
- 17α-Ethynylestradiol
- 19-Nor-17Alpha-Pregna-1,3,5(10)-Trien-20-Yne-3,17,Diol
- 19-Nor-17α-pregna-1,3,5(10)-trien-20-yne-3,17-diol
- 19-Nor-17α-pregna-1,3,5(10)-trien-20-yne-3,17β-diol
- 19-Norpregna-1,3,5(10)-trien-20-yne-3,17-diol, (17alpha)-
- 19-Norpregna-1,3,5(10)-trien-20-yne-3,17-diol, (17α)-
- 3,17Beta-Dihydroxy-17Alpha-Ethynyl-1,3,5(10)-Estratriene
- Acetylene estradiol
- Amenoron
- Anovlar
- Chee-O-Gen
- Chee-O-Genf
- Diognat-E
- Diogyn-E
- Dyloform
- EE
- Esteed
- Estigyn
- Estinyl
- Eston-E
- Estone
- Estoral
- Estoral (Orion)
- Estorals
- Estra-1,3,5(10)-Triene-3,17Beta-Diol, 17Alpha-Ethynyl-
- Estradiol, 17-ethynyl-
- Estroals
- Ethidol
- Ethinoral
- Ethinyl estradiol
- Ethinyloestradiol
- Ethynyl estradiol
- Ethynylestradiol
- Ethynyloestradiol
- Eticyclin
- Eticyclol
- Etinestrol
- Etinestryl
- Etinilestradiol
- Etinoestryl
- Etistradiol
- Feminone
- Follicoral
- Ginestrene
- Gynofen
- Inestra
- Linoral
- Lynoral
- Menolyn
- Microfollin
- Neo-Estrone
- Novestrol
- Novinet
- Nsc 10973
- Oradiol
- Orestralyn
- Palonyl
- Perovex
- Primogyn
- Primogyn C
- Primogyn C(Or M)
- Primogyn M
- Progynon C
- Prosexol
- Roldiol
- Spanestrin
- Voir plus de synonymes
Ethynyl Estradiol
CAS :Produit contrôléApplications Ethynyl Estradiol, an oral contraceptive (1), is a synthetic steroid with high oral estrogenic potency. Used in estrogen replacement therapy. (2)This compound is a contaminant of emerging concern (CECs). Drinking water contaminant candidate list 3 (CCL 3) compound as per United States Environmental Protection Agency (EPA), environmental, and food contaminants.
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package
References 1. Koetsawang, S. et al.: Contraception. 1982 March:25(3) p231-2412. Cuttler, L. et al.: J. Endocrinol. Metab. 1985 Jun;60(6):1087-92.Formule :C20H24O2Couleur et forme :NeatMasse moléculaire :296.4Ethynyl Estradiol-2,4,9,6,6,16,16-d7 (Major)
CAS :Produit contrôléApplications Isotope labelled Ethynyl Estradiol (E685100), an oral contraceptive (1), is a synthetic steroid with high oral estrogenic potency. Used in estrogen replacement therapy (2). Drinking water contaminant candidate list 3 (CCL 3) compound as per United States Environmental Protection Agency (EPA), environmental, and food contaminants.
References 1. Koetsawang, S. et al.: Contraception. 1982 March:25(3) p231-2412. Cuttler, L. et al.: J. Endocrinol. Metab. 1985 Jun;60(6):1087-92.Formule :C20H17D7O2Couleur et forme :NeatMasse moléculaire :303.45(1S,10R,11S,14R,15S)-14-ethynyl-15-methyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadeca-2(7),3,5-triene-5,14-diol
CAS :Formule :C20H24O2Degré de pureté :98%Couleur et forme :LiquidMasse moléculaire :296.41Ethynyl Estradiol-d7
CAS :Produit contrôléFormule :C20D7H17O2Couleur et forme :NeatMasse moléculaire :303.447Ethynylestradiol
CAS :Ethynylestradiol is a synthetic estrogen that is used in hormone replacement therapy. It belongs to the group of estrogens and has been shown to be a potent inhibitor of ovarian activity. Ethinyl estradiol is metabolized through catechol-O-methyltransferase (COMT) and sulfotransferases, which leads to an increased rate constant for its clearance from plasma. The drug also has interactions with other drugs, such as protease inhibitors, which may lead to disease activity or toxicity in the liver. Ethynylestradiol binds specifically to bcl-2 protein, which may be related to its anti-inflammatory properties.
Formule :C20H24O2Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :296.4 g/mol
![(1S,10R,11S,14R,15S)-14-ethynyl-15-methyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadeca-2(7),3,5-tri…](https://static.cymitquimica.com/products/10/thumb/F358085.jpg)
