CAS 54024-17-8
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7 produits concernés.
(8S,9S,10R,14S)-13-Ethyl-11-methylene-7,8,9,10,11,12,13,14,15,16-decahydro-1H-cyclopenta[a]phenanthrene-3,17(2H,6H)-dione
CAS :Formule :C20H26O2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :298.4192Etonogestrel EP Impurity D (Etonogestrel USP Related Compound A)
CAS :Formule :C20H26O2Masse moléculaire :298.4318-Methyl-11-methyleneestr-4-ene-3,17-dione
CAS :Produit contrôléFormule :C20H26O2Couleur et forme :NeatMasse moléculaire :298.42Etonogestrel
CAS :Produit contrôlé<p>Nomegestrol acetate (NET) is a synthetic progestin that is used in combination with an estrogen as hormone replacement therapy in women. It is also used in combination with levonorgestrel to prevent pregnancy. Nomegestrol acetate has been shown to be effective in the treatment of infectious diseases, such as HIV, by reducing viral load and increasing CD4+ T-cell counts. This drug also has contraceptive effects by inhibiting ovulation, thickening cervical mucus, and decreasing the motility of sperm cells. Nomegestrol acetate may cause side-effects such as bleeding and breast tenderness. These side effects are usually temporary but can be severe enough to require discontinuation of the medication. Nomegestrol acetate binds to human serum albumin, which prevents it from being metabolized by cytochrome P450 enzymes, making it a useful tool for detection of these enzymes in blood samples. The drug is also subject to extensive hepatic metabolism</p>Formule :C20H26O2Degré de pureté :Min. 95%Masse moléculaire :298.4 g/molEtonogestrel Related Compound A (13-Ethyl-11-methylenegon-4-ene-3,17-dione)
CAS :Cyclanic, cyclenic or cycloterpenic ketones without other oxygen function, nesoiFormule :C20H26O2Couleur et forme :White PowderMasse moléculaire :298.19328
