-
Succinimide is an
organic compound with the
formula (CH2)2(CO)2NH. This
white solid is used in a
variety of
organic syntheses, as well as in some industrial...
- the epoxide. A
Mitsunobu reaction with
succinimide is performed,
followed by
acidic hydrolysis of the
succinimide protecting group,
hydrolysis of the alkyl...
- chlorinations. It is also used as a mild oxidant. NCS is
related to
succinimide, but with N-Cl in
place of N-H. The N–Cl bond is
highly reactive, and...
- the side
chain of an
asparagine or
aspartic acid residue,
forming a
succinimide intermediate (in red).
Hydrolysis of the
intermediate results in two...
-
peptide group (in
black at top
right of Figure),
forming an
asymmetric succinimide intermediate (in red). The
asymmetry of the
intermediate results in two...
- be
blocked with
certain inhibitors, such as tunicamycin.
deamidation (
succinimide formation) In this modification, an
asparagine or
aspartate side chain...
-
adverse effects on the
fetus during pregnancy.
Ethosuximide is in the
succinimide family of medications. Its
mechanism of
action is
thought to be due to...
- nicotiflorin, and biorobin. Tannins, β-sitosterol, acalyphamide, aurantiamide,
succinimide, and
flindersin (a
pyranoquinolinone alkaloid) have also been isolated...
- (2016). Etiracetam.
Levetiracetam (1999). Seletracetam. The
following are
succinimides:
Ethosuximide (1955). Phensuximide. Mesuximide.
Acetazolamide (1953)...
-
dicarboxylic acids, and
their names reflect the
parent acid.
Examples are
succinimide,
derived from
succinic acid, and phthalimide,
derived from
phthalic acid...
