- ammonia". The
cyclic structure of
hydantoins was
confirmed by
Dorothy Hahn 1913. Of
practical importance,
hydantoins are
obtained by
condensation of a...
-
mechanistically related to them. The
phenylureides are also
closely related to the
hydantoins, such as phenytoin, and may be
considered ring-opened
analogues of them...
-
hydantoin is an
organic compound belonging to a
class of
compounds known as
hydantoins. It is used in the
cosmetics industry and
found in
products like shampoos...
- or
cyanohydrins with
ammonium carbonate and pot****ium
cyanide to give
hydantoins. The
reaction is
named after Hans
Theodor Bucherer.
Following condensation...
- analgesic, anticonvulsant, and
anxiolytic effects. The
following are
hydantoins:
Ethotoin (1957).
Phenytoin (1938). Mephenytoin.
Fosphenytoin (1996)....
- The
Urech hydantoin synthesis is the
chemical reaction of
amino acids with pot****ium
cyanate and
hydrochloric acid to give
hydantoins. Bucherer–Bergs...
-
Fetal hydantoin syndrome, also
called fetal dilantin syndrome, is a
group of
defects caused to the
developing fetus by
exposure to
teratogenic effects...
- ring-opened
analogue of
phenytoin (a
hydantoin), and is
structurally related to the
barbiturates and to
other hydantoins.
Phenacemide was
introduced in 1949...
- any
other hydantoin derivatives are used, then
cardiac monitoring is
necessary if they are
administered intravenously.
Because the
hydantoins take 15–30...
-
Hydantoin racemase (EC 5.1.99.5, 5'-monosubstituted-
hydantoin racemase, HyuA, HyuE) is an
enzyme with
systematic name D-5-monosubstituted-
hydantoin racemase...
