| Weight | 286.371 g/mol |
|---|---|
| Formula | C18H22O3 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
16-Ketoestradiol (566-75-6)
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- The Formation of Five- and Six-membered Rings by the Acyloin Condensation. V. A Novel Conversion of 16-Ketoestradiol-3-methyl Ether to Estrone (Journal of the American Chemical Society, 1957)
- The conversion of estradiol-17beta-16-C14 to radioactive 16-ketoestradiol-17beta-in man. (Journal of Biological Chemistry, 1956)
- Interconversions of 16-oxygenated estrogens. II. The metabolism of 16-ketoestradiol-17-16-C14 in man (Archives of Biochemistry and Biophysics, 1960)
- The synthesis of 16-ketoestradiol-17beta-16-C14. (Journal of Biological Chemistry, 1956)
- Steroid methoximes I: Antifertility activity of methoxime derivatives of progesterone, estrone and 16-ketoestradiol in the rat (Contraception, 1975)
- REDUCTION OF 16-KETOESTRADIOL-17-BETA 16-14C BY MAMMALIAN BLOOD. (Journal of Biological Chemistry, 1964)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC12CCC3C(C1CC(=O)C2O)CCC4=C3C=CC(=C4)O
-
InChIKeyKJDGFQJCHFJTRH-UHFFFAOYSA-N
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