CAS 566-75-6
:16-Cétoestradiol
- (17Beta)-3,17-Dihydroxyestra-1,3,5(10)-Trien-16-One
- (17β)-3,17-Dihydroxyestra-1,3,5(10)-trien-16-one
- (1Beta,3Alpha,5Beta,7Alpha)-1,3,7-Trihydroxycholan-24-Oic Acid
- (2R,3R)-3-hydroxy-2-methylbutanoic acid
- (3Alpha,5Beta,12Beta)-3,12-Dihydroxycholan-24-Oic Acid
- (3Beta,5Alpha,17Alpha)-Androstane-3,17-Diol
- (5R)-5-hydroxyhexanoic acid
- 1,3,5(10)-Estratriene-3,17β-diol-16-one
- 16-Oxo-17β-estradiol
- 16-Oxoestradiol
- 16-Oxoestradiol-17β
- 16-keto-17β-Estradiol
- 3,17-Beta-Dihydroxyoestra-1,3,5(10)-Trien-16-One
- 3,17β-Dihydroxyestra-1,3,5(10)-trien-16-one
- 3-Hydroxydodecanedioic Acid
- Estra-1,3,5(10)-trien-16-one, 3,17-dihydroxy-, (17β)-
- Estra-1,3,5(10)-trien-16-one, 3,17β-dihydroxy-
- NSC 51169
- Voir plus de synonymes
16-Keto-17β-estradiol-2,4,15,15,17-d5
CAS :Degré de pureté :95 atom % DCouleur et forme :White-Yellow SolidMasse moléculaire :291.4016-Oxoestradiol
CAS :Produit contrôléFormule :C18H22O3Couleur et forme :NeatMasse moléculaire :286.3716-Keto 17b-Estradiol (>85%)
CAS :Produit contrôléApplications A metabolite of Estradiol (E888000).
References Ball, P., et al.: Steroids, 33, 563 (1979), Wong, T., et al.: Clin. Chem., 38, 1830 (1992), Xu, X., et al.: J. Clin. Endocrinol. Metab., 84, 3914 (1999), Todorovic, R., et al.: Carcinogenesis, 22, 905 (2001), Travis, R., et al.: Breast Cancer Res., 5, 239 (2003),Formule :C18H22O3Degré de pureté :>85%Couleur et forme :NeatMasse moléculaire :286.3716-Keto 17beta-Estradiol-d5 (Major)
CAS :Produit contrôléApplications A labelled metabolite of Estradiol (E888000).
References Ball, P., et al.: Steroids, 33, 563 (1979), Wong, T., et al.: Clin. Chem., 38, 1830 (1992), Xu, X., et al.: J. Clin. Endocrinol. Metab., 84, 3914 (1999), Todorovic, R., et al.: Carcinogenesis, 22, 905 (2001), Travis, R., et al.: Breast Cancer Res., 5, 239 (2003),Formule :C18H17D5O3Couleur et forme :NeatMasse moléculaire :291.416-Keto-17β-estradiol
CAS :Produit contrôlé16-Keto 17b-estradiol (16KE) is a potent estrogen that binds to the estrogen receptor and inhibits the binding of other estrogens. 16KE has been shown to be effective in inhibiting the growth of Streptococcus faecalis, which is often found in urine samples or as a result of bacterial vaginosis. 16KE also has an anti-angiogenic effect, which may be due to its ability to inhibit angiogenic factors such as vascular endothelial growth factor and angiopoietin 2. 16KE also has hormonal effects on adrenocortical carcinoma cells, leading to decreased cell proliferation and increased apoptosis. This compound may also have an anti-cancer effect by inducing apoptosis and suppressing tumor growth through the inhibition of cancer cell proliferation and stimulation of cancer cell death.
Formule :C18H22O3Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :286.37 g/mol





