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valofane

Known as: 2-allophenyl-2-allyl-gamma-valerolactone, valofan, allophanyl allyl valerolactone 
National Institutes of Health

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2 relations

Broader (1)

Urea
analogs & derivatives

Papers overview

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2017
2017
Degradable polyesters via ring-opening polymerization of functional valerolactones for efficient gene delivery.
Degradable polymers as gene and drug carriers are emerging as one of the most promising types of materials in the biomedical and… 
2008
2008
Why d-Valerolactone Polymerizes and ?-Butyrolactone Does Not
1987
1987
Effects of 2-allophanyl-2-allyl-4-valerolactone (valofan) on cerebral energy metabolism of rat in normoxia and hypobaric hypoxia.
The effects of an atypical barbiturate, valofan, and of a classical barbiturate, exobarbital, on the cerebral energy metabolism… 
1987
1987
Effects of an atypical barbiturate (valofan) on spontaneous and stimulated locomotor activity and on brain serotonin metabolism in mice.
The effects of an atypical barbiturate, 2-allophanyl-2-allyl-4-valerolactone (valofan), have been studied on spontaneous… 
1985
1985
Effect of an atypical barbiturate, the 2-allophanyl-2-allyl-4-valerolactone (valofan), on exploratory behaviour and brain serotonin concentrations in mice.
This study investigates, both behaviourally and biochemically, the action of 2-allophanyl-2-allyl-4-valerolactone (Valofan) in… 
1984
1984
Isomerisation and urinary excretion of proxibarbal and valofan in man; a preliminary study
SummaryProxibarbal and valofan are tautomeric drμgs which interconvert rapidly in solution. In the present study, the urinary… 
1984
1984
[Development of proxibarbal blood levels. The role of various elimination processes].
Half-lives of barbiturates are short when their lipid solubility is high but long when they are less lipophilic. Infection of… 
1979
1979
Central properties of alpha-allophanyl-alpha-allyl-gamma-valerolactone (valofan) [proceedings].
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