3,4-epoxy-3-methyl-1-butene has been researched along with phenobarbital in 1 studies
*Phenobarbital: A barbituric acid derivative that acts as a nonselective central nervous system depressant. It potentiates GAMMA-AMINOBUTYRIC ACID action on GABA-A RECEPTORS, and modulates chloride currents through receptor channels. It also inhibits glutamate induced depolarizations. [MeSH]
*Phenobarbital: A barbituric acid derivative that acts as a nonselective central nervous system depressant. It potentiates GAMMA-AMINOBUTYRIC ACID action on GABA-A RECEPTORS, and modulates chloride currents through receptor channels. It also inhibits glutamate induced depolarizations. [MeSH]
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Amato, G; Chiappe, C; De Rubertis, A; Gervasi, PG; Tinagli, V | 1 |
1 other study(ies) available for 3,4-epoxy-3-methyl-1-butene and phenobarbital
| Article | Year |
|---|---|
Stereochemical course of the biotransformation of isoprene monoepoxides and of the corresponding diols with liver microsomes from control and induced rats.
Topics: Animals; Biotransformation; Butadienes; Chromatography, Gas; Cytochrome P-450 Enzyme System; Enzyme Induction; Epoxy Compounds; Hemiterpenes; Male; Microsomes, Liver; Pentanes; Phenobarbital; Pyrenes; Rats; Rats, Sprague-Dawley; Stereoisomerism | 2000 |