-
Barbital (or barbitone), sold
under the
brand names Veronal for the pure acid and
Medinal for the
sodium salt, was the
first commercially available barbiturate...
-
interactions [1]
calculated with
CrystalExplorer Program.
Sodium barbital and
barbital have also been used as pH
buffers for
biological research, e.g....
- Bar-Test
barasertib (INN)
barbexaclone (INN)
Barbidonna Barbita barbital sodium (INN)
barbital (INN) Barc
Liquid Bardoxolone (USAN, INN)
Baricon barixibat...
-
observations that
barbital (then
known as diethyl-barbituric acid) has
sedative properties in humans. In 1904, he
helped to
launch barbital under the brand...
- than
phenobarbital and
barbital (in
descending order). (Secobarbital >
pentobarbital >
amobarbital >
phenobarbital >
barbital) It has an LD50 in mice...
-
analogue of
barbital. It is of note that
although the drug can be
prepared by the
above route (cf e.g. thialbarbital),
reaction of
barbital with phosphorus...
-
Cosmetics Rules 1945: The list of
Schedule X drugs:
Amobarbital Amphetamine Barbital Cyclobarbital Dexamphetamine Ethchlorvynol Glutethimide Ketamine Meprobamate...
-
after him. He took his own life at the age of 35
through an
overdose of
barbital. Ryūnosuke
Akutagawa was born in Irifune, Kyōbashi,
Tokyo City (present-day...
- is a
derivative of
diethyl malonate. It can be used in the
synthesis of
barbital. As
being a
diethyl malonate derivative, it can be
combined with urea under...
-
discovered to have
medical use in 1903, when a
research at
Bayer showed barbital to be an
effective sedative for dogs. It was not
until the mid 20th century...