Clinical data | |
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Other names | Proxibarbital, Centralgol, Ipronal, 5-Allyl-5-(β-hydroxypropyl)barbituric acid |
ATC code | |
Identifiers | |
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CAS Number | |
PubChem CID | |
ChemSpider | |
UNII | |
ChEMBL | |
CompTox Dashboard ( EPA) | |
ECHA InfoCard | 100.018.004 |
Chemical and physical data | |
Formula | C10H14N2O4 |
Molar mass | 226.232 g·mol−1 |
3D model ( JSmol) | |
| |
| |
(what is this?) (verify) |
Proxibarbital (Ipronal) is a barbiturate derivative synthesized in 1956. It has anti-anxiety properties and is, in contrast to most barbiturates, almost without hypnotic action. [1]
It was also used in the treatment of migraine headaches in a similar manner to butalbital. [2]
Valofane isomerises to Proxibarbal in vivo.
{{
cite book}}
: CS1 maint: location missing publisher (
link)
Clinical data | |
---|---|
Other names | Proxibarbital, Centralgol, Ipronal, 5-Allyl-5-(β-hydroxypropyl)barbituric acid |
ATC code | |
Identifiers | |
| |
CAS Number | |
PubChem CID | |
ChemSpider | |
UNII | |
ChEMBL | |
CompTox Dashboard ( EPA) | |
ECHA InfoCard | 100.018.004 |
Chemical and physical data | |
Formula | C10H14N2O4 |
Molar mass | 226.232 g·mol−1 |
3D model ( JSmol) | |
| |
| |
(what is this?) (verify) |
Proxibarbital (Ipronal) is a barbiturate derivative synthesized in 1956. It has anti-anxiety properties and is, in contrast to most barbiturates, almost without hypnotic action. [1]
It was also used in the treatment of migraine headaches in a similar manner to butalbital. [2]
Valofane isomerises to Proxibarbal in vivo.
{{
cite book}}
: CS1 maint: location missing publisher (
link)