Page last updated: 2024-12-04

succinic semialdehyde

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

Description

succinic semialdehyde: structure [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID1112
CHEMBL ID1615238
CHEBI ID16265
SCHEMBL ID59553
MeSH IDM0053939

Synonyms (47)

Synonym
SSN ,
3-formylpropanoic acid
4-oxobutanoic acid
succinic acid semialdehyde
CHEBI:16265 ,
beta-formylpropionic acid
semialdehyde succinique
succinaldehydic acid
3-formylpropionic acid
brn 1745187
succinic semialdehyde monomer
butryaldehydic acid
semi-aldehyde succinique [french]
4-03-00-01554 (beilstein handbook reference)
butanoic acid, 4-oxo-
gamma-oxybutyric acid
4-oxobutyric acid
succinate semialdehyde
succinic semialdehyde
692-29-5
C00232 ,
75002101-E68F-401B-8773-972512002B60
LMFA06000118
4-oxo-butanoic acid
4-oxo-butyric acid
CHEMBL1615238
AKOS006223730
m73bx3cpmu ,
semi-aldehyde succinique
unii-m73bx3cpmu
FT-0632816
SCHEMBL59553
4-ketobutyric acid
UIUJIQZEACWQSV-UHFFFAOYSA-N
DTXSID00219231
HY-104071
CS-0028111
beta-formylpropionate
succinaldehydate
butryaldehydate
3-formylpropanoate
gamma-oxybutyrate
Q4602542
succinaldehydicacid
4-oxobutanoicacid
EN300-66985
PD026754

Research Excerpts

[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (2)

RoleDescription
Escherichia coli metaboliteAny bacterial metabolite produced during a metabolic reaction in Escherichia coli.
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 (1)

ClassDescription
aldehydic acidA monocarboxylic acid derived from any dicarboxylic acid that has a retained name by the formal reduction of one of the carboxy groups to a formyl group. The resulting structure, also known as a semialdehyde, may be named by replacing the ending '...ic acid' of the retained name of the dicarboxylic acid by the ending '...aldehydic acid'. Aldehydic acids therefore contain one carboxy group and one aldehyde group.
[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]

Pathways (22)

PathwayProteinsCompounds
Glutamate Metabolism2244
4-Hydroxybutyric Aciduria/Succinic Semialdehyde Dehydrogenase Deficiency2244
Homocarnosinosis2244
Hyperinsulinism-Hyperammonemia Syndrome2244
2-Hydroxyglutric Aciduria (D and L Form)2244
Succinic Semialdehyde Dehydrogenase Deficiency2244
Arginine Metabolism2848
Ornithine Metabolism1631
4-Aminobutanoate Degradation I39
4-Aminobutanoate Degradation29
Glutamic Acid Metabolism1317
Butanoate Metabolism922
2-Oxo-glutaric acid + 4-Amino-butanoic acid = L-Glutamic acid + Succinate semialdehyde ( Glutamic acid and Glutamine metabolism )14
Glutamic acid and Glutamine metabolism ( Glutamic acid and Glutamine metabolism )1926
NAD+ + Succinate semialdehyde + H2O = NADH + Succinic acid ( Glutamic acid and Glutamine metabolism )15
superpathway of 4-aminobutyrate degradation011
4-aminobutyrate degradation I09
4-aminobutyrate degradation II09
superpathway of arginine and ornithine degradation027
superpathway of arginine, putrescine, and 4-aminobutyrate degradation026
GABA degradation09
Biochemical pathways: part I0466

Research

Studies (82)

TimeframeStudies, This Drug (%)All Drugs %
pre-199034 (41.46)18.7374
1990's5 (6.10)18.2507
2000's18 (21.95)29.6817
2010's23 (28.05)24.3611
2020's2 (2.44)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 52.13

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 very strong demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index52.13 (24.57)
Research Supply Index4.50 (2.92)
Research Growth Index4.76 (4.65)
Search Engine Demand Index79.60 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (52.13)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials1 (1.14%)5.53%
Reviews2 (2.27%)6.00%
Case Studies2 (2.27%)4.05%
Observational0 (0.00%)0.25%
Other83 (94.32%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]