Weight | 387.524 g/mol |
---|---|
Formula | C22H33N3O3 |
Hydrogen Acceptors | 4 |
Hydrogen Donors | 3 |
Aromatic Rings | 1 |
Rotatable Bonds | 5 |
Barbexaclone (4388-82-3)
phenobarbital propylhexedrine salt · CHP phenobarbital · Maliasin
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- Pharmacokinetics of phenobarbital and propylhexedrine after administration of barbexaclone in the mouse (Naunyn-schmiedebergs Archives of Pharmacology, 1983)
- Ensaio clnico com barbexaclone nas epilepsias (Arquivos De Neuro-psiquiatria, 1977)
- Comparative kinetics of phenobarbital after administration of the acid and the propylhexedrine salt (barbexaclone) (European Journal of Clinical Pharmacology, 1986)
- A comparison of the anticonvulsant properties of l-propylhexedrine, phenobarbital and a salt-like complex of l-propylhexedrine and phenobarbital in mice and rats. (Archives internationales de pharmacodynamie et de thrapie, 1967)
- Ensaio clnico com um novo anti-epilptico (barbexaclone) (Arquivos De Neuro-psiquiatria, 1977)
- Reavaliao do barbexaclone em 20 pacientes epileticos (Arquivos De Neuro-psiquiatria, 1978)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - phenobarbital propylhexedrine salt
- CHP phenobarbital
- Maliasin
- BC brand of barbexaclone
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SMILESCCC1(C(=O)NC(=O)NC1=O)C2=CC=CC=C2.CC(CC1CCCCC1)NC
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InChIKeyMJCBWPMBFCUHBP-UHFFFAOYSA-N
- Pubchem - Barbexaclone
- Wikipedia - barbexaclone
Barbexaclone (Maliasin) is a salt compound of phenobarbital and levopropylhexedrine. It was introduced in 1983. It has been reported to be as effective as phenobarbital but better tolerated; however, as of 2004, these "promising results" had not yet been confirmed nor denied in controlled trials.
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