3913-64-2
3913-64-2
Chemical Structure
L-Lactaldehyde
Synonym(s): (2S)-Hydroxypropanal
- CAS No.: 3913-64-2
- Formula:C3H6O2
- Molecular Weight:74.08
InChIKey: BSABBBMNWQWLLU-VKHMYHEASA-N
SMILES: O=C[C@@H](O)C
Biological Activity: L-Lactaldehyde ((2S)-Hydroxypropanal) is a chiral aldehyde, metabolic intermediate, and enzyme substrate. L-Lactaldehyde is oxidized to L-lactate by NAD-dependent lactaldehyde dehydrogenase. L-Lactaldehyde is reduced to L-1,2-propanediol by NADH/NADPH-dependent oxidoreductases. L-Lactaldehyde is used in studies of microbial sugar metabolism and carbonyl metabolism[1][2][3].
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L-Lactaldehyde | L-Lactaldehyde ((2S)-Hydroxypropanal) is a chiral aldehyde, metabolic intermediate, and enzyme substrate. L-Lactaldehyde is oxidized to L-lactate by NAD-dependent lactaldehyde dehydrogenase. L-Lactaldehyde is reduced to L-1,2-propanediol by NADH/NADPH-dependent oxidoreductases. L-Lactaldehyde is used in studies of microbial sugar metabolism and carbonyl metabolism. | |||||||||||||||||||||
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References
- [1]. Sato K, et al. Purification and characterization of dimeric dihydrodiol dehydrogenase from dog liver. Journal of biochemistry. 1994 Sep;116(3):711-7. [Content Brief]
- [2]. Boronat A, et al. Rhamnose-induced propanediol oxidoreductase in Escherichia coli: purification, properties, and comparison with the fucose-induced enzyme. Journal of bacteriology. 1979 Nov;140(2):320-6. [Content Brief]
- [3]. Inoue Y, et al. Metabolism of 2-oxoaldehydes in yeasts. Purification and characterization of lactaldehyde dehydrogenase from Saccharomyces cerevisiae. European journal of biochemistry. 1985 Dec 02;153(2):243-7. [Content Brief]
