| Weight | 302.458 g/mol |
|---|---|
| Formula | C20H30O2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 1 |
NORETHANDROLONE (52-78-8)
Nilevar · Ethylnortestosterone · Norethandrolone Laphal Brand
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- Cholestasis produced by the administration of norethandrolone (The American Journal of Medicine, 1959)
- II. The effect of D-thyroxine, clofibrate, and norethandrolone (Clinical Pharmacology & Therapeutics, 1967)
- Peliosis hepatis and cholestasis following administration of norethandrolone. (American Journal of Clinical Pathology, 1960)
- Changes in bile canaliculi produced by norethandrolone: electron microscopic study of human and rat liver. (Journal of Laboratory and Clinical Medicine, 1960)
- A six-month evaluation of an anabolic drug, norethandrolone, in underweight persons. II. Bromsulphalein (BSP) retention and liver function (The American Journal of Medicine, 1959)
- Effects of Norethandrolone on the Transport in Serum and Peripheral Turnover of Thyroxine (The Journal of Clinical Endocrinology and Metabolism, 1967)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Nilevar
- Ethylnortestosterone
- Norethandrolone Laphal Brand
- Ethylestrenolone
- Laphal Brand of Norethandrolone
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SMILESCCC1(CCC2C1(CCC3C2CCC4=CC(=O)CCC34)C)O
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InChIKeyZDHCJEIGTNNEMY-UHFFFAOYSA-N
- Pubchem - NORETHANDROLONE
- Wikipedia - norethandrolone
Norethandrolone, sold under the brand names Nilevar and Pronabol, is an androgen and anabolic steroid (AAS) and progestogen which has mostly been discontinued but is still used in France.
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