Weight | 210.233 g/mol |
---|---|
Formula | C10H14N2O3 |
Hydrogen Acceptors | 3 |
Hydrogen Donors | 2 |
Aromatic Rings | 0 |
Rotatable Bonds | 3 |
APROBARBITAL (77-02-1)
allylpropymal, monosodium salt · allylpropymal · aprobarbitone
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- Enhancement of hepatocarcinogenesis and induction of specific cytochrome P450-dependent monooxygenase activities by the barbiturates allobarbital, aprobarbital, pentobarbital, secobarbital and 5-phenyl- and 5-ethylbarbituric acids (Carcinogenesis, 1994)
- Experimental investigations into the effects of morphine and aprobarbital on carbon-dioxide provoked pulmonary oedema in mice. (Pharmacology & Toxicology, 2009)
- Chlorzoxazone mimics aprobarbital in Toxi-Lab Drug Screen. (Clinical Chemistry, 1984)
- Antaraksi Fisik Padatan Pada Kombinasi Senyawa Aprobarbital dan Isopropilantipirina (2009)
- Oramon poisoning in infancy and childhood. Observations on 12 aprobarbital poisonings (Das Deutsche Gesundheitswesen, 1966)
- An Unstable Modification of Aprobarbital (Nature, 1957)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - allylpropymal, monosodium salt
- allylpropymal
- aprobarbitone
-
SMILESCC(C)C1(C(=O)NC(=O)NC1=O)CC=C
-
InChIKeyUORJNBVJVRLXMQ-UHFFFAOYSA-N
- Pubchem - APROBARBITAL
- Wikipedia - aprobarbital
Aprobarbital (or aprobarbitone), sold as Oramon, Somnifaine, and Allonal, is a barbiturate derivative invented in the 1920s by Ernst Preiswerk. It has sedative, hypnotic and anticonvulsant properties, and was used primarily for the treatment of insomnia. Aprobarbital was never as widely used as more common barbiturate derivatives such as phenobarbital and is now rarely prescribed as it has been replaced by newer drugs with a better safety margin.
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