| Weight | 183.251 g/mol |
|---|---|
| Formula | C10H17NO2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 2 |
methyprylon (125-64-4)
Noludar · methprylon
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- Hypnotics and Altered Sleep-Dream Patterns: I. All-night EEG Studies of Glutethimide, Methyprylon, and Pentobarbital (Archives of General Psychiatry, 1970)
- A study of hypnotic drugs in patients with chronic diseases: Comparative efficacy of placebo; methyprylon (Noludar); meprobamate (Miltown, Equanil) pentobarbital; phenobarbital; secobarbital (Journal of Chronic Diseases, 1956)
- Methaqualone, methyprylon, and glutethimide clearance by the ACAC microcapsule artificial kidney: in vitro and in patients with acute intoxication. (Asaio Journal, 1973)
- Enhanced metabolism of methyprylon, meprobamate, and chlordiazepoxide hydrochloride after chronic feeding of a low dietary level of DDT to male and female rats (Toxicology and Applied Pharmacology, 1968)
- Fatal poisoning with methyprylon (nodular), a nonbarbiturate sedative. (The New England Journal of Medicine, 1956)
- CENTRAL DEPRESSANT EFFECTS OF METHYPRYLON (Journal of Pharmacology and Experimental Therapeutics, 1956)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Noludar
- methprylon
-
SMILESCCC1(C(=O)C(CNC1=O)C)CC
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InChIKeySIDLZWOQUZRBRU-UHFFFAOYSA-N
- Pubchem - methyprylon
- Wikipedia - methyprylon
Methyprylon (Noludar) is a sedative of the piperidinedione derivative family developed by Hoffmann-La Roche. This medicine was used for treating insomnia, but is now rarely used as it has been replaced by newer drugs with fewer side effects, such as benzodiazepines. Methyprylon was withdrawn from the US market in June 1989 and the Canadian market in September 1990.
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