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Chemical compound
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
Aminoacetone
Class of organic compounds
aminoaldehyde. The compound is unstable with respect to self-condensation. Aminoacetone is a prominent member of this class of compounds. It is unstable under
Aminoaldehydes and aminoketones
Aminoaldehydes_and_aminoketones
Class of enzymes
the chemical reaction (2R)-1-aminopropan-2-ol + NAD+ H+ H+ aminoacetone + NADH The two substrates of this enzyme are (2R)-1-aminopropan-2-ol
(R)-aminopropanol dehydrogenase
(R)-aminopropanol_dehydrogenase
Vitamin
several steps and a convergence of two branches, one producing 3-hydroxy-1-aminoacetone phosphate from erythrose 4-phosphate, while the other (single enzyme)
Pyridoxal_phosphate
Organic reaction of carbonyl compounds with amines to imines
cannot carry simultaneously (unprotected) aldehyde and amine groups. Aminoacetone, the simplest amino ketone, cannot be isolated as a liquid or solid,
Carbonyl_condensation
Chemical compound
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
Methylglyoxal
ligase, 2-amino-3-ketobutyrate-CoA ligase, glycine acetyltransferase, and aminoacetone synthase. This enzyme and L-threonine 3-dehydrogenase act together to
Glycine_C-acetyltransferase
Chemical compound
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
Erythrose_4-phosphate
Protein-coding gene in the species Homo sapiens
"Interaction between L-threonine dehydrogenase and aminoacetone synthetase and mechanism of aminoacetone production". The Journal of Biological Chemistry
GCAT
Class of enzymes
catalyzes the chemical reaction 1-deoxy-D-xylulose 5-phosphate + 3-hydroxy-1-aminoacetone phosphate ⇌ {\displaystyle \rightleftharpoons } pyridoxine-5'-phosphate
Pyridoxine 5'-phosphate synthase
Pyridoxine_5'-phosphate_synthase
Chemical compound
pharmaceutical drugs.[citation needed] (R)-1-aminopropan-2-ol is metabolised to aminoacetone by the enzyme (R)-aminopropanol dehydrogenase. Synthesis of Hexylcaine
1-Aminopropan-2-ol
Enzyme
catalyzes the oxidative conversion of primary amines (methylamine and aminoacetone) to aldehydes (formaldehyde and methylglyoxal) ammonium and hydrogen
AOC3
Class of enzymes
Pathway Database. Green ML, Elliott WH (1964). "The enzymic formation of aminoacetone from threonine and its further metabolism". Biochem. J. 92 (3): 537–49
L-threonine_3-dehydrogenase
Protein
(deaminating) activity copper ion binding metal ion binding quinone binding aminoacetone:oxygen oxidoreductase(deaminating) activity primary amine oxidase activity
AOC2
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