| Weight | 286.371 g/mol |
|---|---|
| Formula | C18H22O3 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 5 |
METHALLENESTRIL (517-18-0)
Vallestril · methallenestril, (+)-isomer · methallenestril, (+-)-isomer
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- Normalization of Hypercalcaemia of Primary Hyperparathyroidism by Treatment with Methallenestril, a Synthetic Oestrogen with Low Oestrogenicity (Urologia Internationalis, 1983)
- Clinical Assay of a New Synthetic Estrogen: Vallestril (The New England Journal of Medicine, 1952)
- Methallenestril, a new synthetic estrogen. (JAMA, 1956)
- The first one-pot asymmetric synthesis of esters of highly biologically active (+)- and (-)- 3-[2-(6-methoxynaphthyl)]-2,2-dimethylpentanoic acid (Vallestril) (Arkivoc, 2000)
- Clinical evaluation of a new synthetic estrogen, Vallestril. (Journal of the Japanese Obstetrical & Gynecological Society, 1954)
- Dimethyl-ethyl-allenolic acid (Vallestril) (1956)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Vallestril
- methallenestril, (+)-isomer
- methallenestril, (+-)-isomer
- methallenestril, (-)-isomer
-
SMILESCCC(C1=CC2=C(C=C1)C=C(C=C2)OC)C(C)(C)C(=O)O
-
InChIKeyKHLJKRBMZVNZOC-UHFFFAOYSA-N
- Pubchem - METHALLENESTRIL
- Wikipedia - methallenestril
Methallenestril (INN) (brand names Cur-men, Ercostrol, Geklimon, Novestrine, Vallestril), also known as methallenoestril (BAN) and as methallenestrol, as well as Horeau's acid, is a synthetic nonsteroidal estrogen and a derivative of allenolic acid and allenestrol (specifically, a methyl ether of it) that was formerly used to treat menstrual issues but is now no longer marketed. It is a seco-analogue of bisdehydrodoisynolic acid, and although methallenestril is potently estrogenic in rats, in humans it is only weakly so in comparison. Vallestril was a brand of methallenestril issued by G.
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