-
Aminoacetone is the
organic compound with the
formula CH3C(O)CH2NH2.
Although stable in the
gaseous form, once
condensed it
reacts with itself. The protonated...
- aminoaldehyde. The
compound is
unstable with
respect to self-condensation
Aminoacetone is a
prominent member of this
class of compounds. It is
unstable under...
-
several steps and a
convergence of two branches, one
producing 3-hydroxy-1-
aminoacetone phosphate from
erythrose 4-phosphate,
while the
other (single enzyme)...
-
cannot carry simultaneously (unprotected)
aldehyde and
amine groups.
Aminoacetone, the
simplest amino ketone,
cannot be
isolated as a
liquid or solid,...
- "Interaction
between L-threonine
dehydrogenase and
aminoacetone synthetase and
mechanism of
aminoacetone production". The
Journal of
Biological Chemistry...
- to 231 μg/mg of
kidney protein in
poisoned mice. It may form from 3-
aminoacetone,
which is an
intermediate of
threonine catabolism, as well as through...
-
pharmaceutical drugs.[citation needed] (R)-1-aminopropan-2-ol is
metabolised to
aminoacetone by the
enzyme (R)-aminopropanol dehydrogenase.
Synthesis of Hexylcaine...
-
reaction catalyzed by the
enzyme DAHP synthase. It also used in 3-hydroxy-1-
aminoacetone phosphate biosynthesis,
which is a
precursor of
vitamin B6 in DXP-dependent...
- \rightleftharpoons }
aminoacetone + NADH + H+ Thus, the two
substrates of this
enzyme are (R)-1-aminopropan-2-ol and NAD+,
whereas its 3
products are
aminoacetone, NADH...
- 2DFV, and 2DQ4.
Green ML,
Elliott WH (1964). "The
enzymic formation of
aminoacetone from
threonine and its
further metabolism". Biochem. J. 92 (3): 537–49...
