| Weight | 272.388 g/mol |
|---|---|
| Formula | C18H24O2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
19-Norandrostenedione (734-32-7)
19-nor-A-dione · 19-norandrost-4-ene-3,17-dione · 19-nor-4-androstene-3,17-dione
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- The Facile Synthesis of 19-Nortestosterone and 19-Norandrostenedione from Estrone (Journal of the American Chemical Society, 1953)
- Identification and measurement of 4-oestren-3,17-dione (19-norandrostenedione) in porcine ovarian follicular fluid using high performance liquid chromatography and capillary gas chromatographymass spectrometry (Journal of Endocrinology, 1985)
- Identification of 19-Norandrostenedione in Follicular Fluid (Nature, 1960)
- Studies related to the origin of C18 neutral steroids isolated from extracts of urine from the male horse: The identification of urinary 19-oic acids and their decarboxylation to produce estr-4-en-17-ol-3-one (19-nortestosterone) and estr-4-ene-3,17-dione (19-norandrost-4-ene-3,17-dione) during sample processing (Analytica Chimica Acta, 2007)
- Formation of 4-oestrene-3,17-dione (19-norandrostenedione) by porcine granulosa cells in vitro is inhibited by the aromatase inhibitor 4-hydroxyandrostenedione and the cytochrome P-450 inhibitors aminoglutethimide phosphate and ketoconazole (Journal of Endocrinology, 1989)
- Displacement of carbon monoxide from placental cytochrome P-450 by steroids: Antagonistic effects of androstenedione and 19-norandrostenedione (Biochemical and Biophysical Research Communications, 1975)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 19-nor-A-dione
- 19-norandrost-4-ene-3,17-dione
- 19-nor-4-androstene-3,17-dione
-
SMILESCC12CCC3C(C1CCC2=O)CCC4=CC(=O)CCC34
-
InChIKeyJRIZOGLBRPZBLQ-UHFFFAOYSA-N
- Pubchem - 19-Norandrostenedione
- Wikipedia - 19-norandrostenedione
19-Norandrostenedione may refer to: Bolandione (19-nor-4-androstenedione) 19-Nor-5-androstenedione
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