Page last updated: 2024-12-04

lactaldehyde

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth Market Indicators

Description

lactaldehyde : A member of the class of propanals obtained by the reduction of the carboxylic group of lactic acid (2-hydroxypropanoic acid). [Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Cross-References

ID SourceID
PubMed CID855
CHEBI ID18419
MeSH IDM0063323

Synonyms (24)

Synonym
CHEBI:18419
propanal, 2-hydroxy- (9ci)
dl-lactaldehyde
racemic-glycerol formal
lactaldehyde (6ci,7ci,8ci)
propanal, 2-hydroxy
lactaldehyde
2-hydroxypropionaldehyde
C05999
598-35-6
2-hydroxypropanal
HYDROXYPROPANAL ,
s468fb0qe4 ,
propanal, 2-hydroxy-
propanal, 2-hydroxy-, (+-)-
unii-s468fb0qe4
AKOS015329096
BSABBBMNWQWLLU-UHFFFAOYSA-N
Q4381828
lactaldehyde, (+/-)-
lactaldehyde, dl-
DTXSID60862267
A901946
EN300-1600489

Research Excerpts

Overview

L-Lactaldehyde is a branching point in the metabolic pathway of L-fucose and L-rhamnose utilization.

ExcerptReferenceRelevance
"L-Lactaldehyde is a branching point in the metabolic pathway of L-fucose and L-rhamnose utilization. "( Metabolism of L-fucose and L-rhamnose in Escherichia coli: aerobic-anaerobic regulation of L-lactaldehyde dissimilation.
Aguilar, J; Baldomà, L, 1988
)
1.22
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (1)

RoleDescription
mouse metaboliteAny mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).
[role information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Drug Classes (2)

ClassDescription
propanalsAn aldehyde based on a propanal skeleton and its derivatives.
hydroxyaldehyde
[compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Research

Studies (32)

TimeframeStudies, This Drug (%)All Drugs %
pre-199014 (43.75)18.7374
1990's4 (12.50)18.2507
2000's8 (25.00)29.6817
2010's5 (15.63)24.3611
2020's1 (3.13)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 31.25

According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be moderate demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index31.25 (24.57)
Research Supply Index3.50 (2.92)
Research Growth Index4.53 (4.65)
Search Engine Demand Index37.30 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (31.25)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other32 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]