Page last updated: 2024-12-04

n(1)-acetylspermidine

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

Description

N(1)-acetylspermidine : An acetylspermidine having the acetyl group at the N1-position. [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 CID496
CHEMBL ID176800
CHEBI ID17927
SCHEMBL ID183048
MeSH IDM0069183

Synonyms (24)

Synonym
n(1)-acetylspermidine
14278-49-0
1-n-acetylspermidine
CHEBI:17927 ,
n-{3-[(4-aminobutyl)amino]propyl}acetamide
n1-acetylspermidine
C00612
CHEMBL176800 ,
n-[3-(4-aminobutylamino)propyl]acetamide
n-(3-((4-aminobutyl)amino)propyl)-acetamide
n-(3-((4-aminobutyl)amino)propyl)acetamide
acetamide, n-(3-((4-aminobutyl)amino)propyl)-
n-acetylspermidine
bdbm50405933
SCHEMBL183048
AKOS024183045
acetamide,n-(3-((4-aminobutyl)amino)propyl)-
DTXSID80162175
acetamide, n-[3-[(4-aminobutyl)amino]propyl]-
n-{3-[(4-aminobutyl)amino]propyl}acetamide hydrochloride
Q3869337
n-(3-((4-aminobutyl)amino)propyl)acetamide 2hcl
hlg ,
A908956
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (2)

RoleDescription
metaboliteAny intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
Escherichia coli metaboliteAny bacterial metabolite produced during a metabolic reaction in Escherichia coli.
[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
acetylspermidine
[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 (8)

PathwayProteinsCompounds
Metabolism14961108
Amino acid and derivative metabolism250260
Metabolism of polyamines5621
Interconversion of polyamines313
Biological oxidations150276
Phase I - Functionalization of compounds69175
Amine Oxidase reactions419
PAOs oxidise polyamines to amines211

Protein Targets (1)

Inhibition Measurements

ProteinTaxonomyMeasurementAverageMin (ref.)Avg (ref.)Max (ref.)Bioassay(s)
Peroxisomal N(1)-acetyl-spermine/spermidine oxidaseHomo sapiens (human)Ki1,370.00000.10000.27670.5500AID144352
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Biological Processes (5)

Processvia Protein(s)Taxonomy
putrescine biosynthetic processPeroxisomal N(1)-acetyl-spermine/spermidine oxidaseHomo sapiens (human)
putrescine catabolic processPeroxisomal N(1)-acetyl-spermine/spermidine oxidaseHomo sapiens (human)
spermidine catabolic processPeroxisomal N(1)-acetyl-spermine/spermidine oxidaseHomo sapiens (human)
spermine catabolic processPeroxisomal N(1)-acetyl-spermine/spermidine oxidaseHomo sapiens (human)
positive regulation of spermidine biosynthetic processPeroxisomal N(1)-acetyl-spermine/spermidine oxidaseHomo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Molecular Functions (6)

Processvia Protein(s)Taxonomy
polyamine oxidase activityPeroxisomal N(1)-acetyl-spermine/spermidine oxidaseHomo sapiens (human)
N(1),N(12)-diacetylspermine:oxygen oxidoreductase (3-acetamidopropanal-forming) activityPeroxisomal N(1)-acetyl-spermine/spermidine oxidaseHomo sapiens (human)
spermine:oxygen oxidoreductase (spermidine-forming) activityPeroxisomal N(1)-acetyl-spermine/spermidine oxidaseHomo sapiens (human)
spermidine:oxygen oxidoreductase (3-aminopropanal-forming) activityPeroxisomal N(1)-acetyl-spermine/spermidine oxidaseHomo sapiens (human)
N1-acetylspermine:oxygen oxidoreductase (3-acetamidopropanal-forming) activityPeroxisomal N(1)-acetyl-spermine/spermidine oxidaseHomo sapiens (human)
N1-acetylspermidine:oxygen oxidoreductase (3-acetamidopropanal-forming) activityPeroxisomal N(1)-acetyl-spermine/spermidine oxidaseHomo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Ceullar Components (2)

Processvia Protein(s)Taxonomy
peroxisomal matrixPeroxisomal N(1)-acetyl-spermine/spermidine oxidaseHomo sapiens (human)
cytosolPeroxisomal N(1)-acetyl-spermine/spermidine oxidaseHomo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Bioassays (5)

Assay IDTitleYearJournalArticle
AID1210039Drug level in human HepG2 cells assessed as SSAT2-mediated compound formation treated with TETA at 1 mM for 24 hrs2013Drug metabolism and disposition: the biological fate of chemicals, Jan, Volume: 41, Issue:1
Metabolism of triethylenetetramine and 1,12-diamino-3,6,9-triazadodecane by the spermidine/spermine-N(1)-acetyltransferase and thialysine acetyltransferase.
AID1210040Drug level in human HepG2 cells assessed as SSAT1-mediated compound formation treated with SpmTrien at 100 uM for 24 hrs2013Drug metabolism and disposition: the biological fate of chemicals, Jan, Volume: 41, Issue:1
Metabolism of triethylenetetramine and 1,12-diamino-3,6,9-triazadodecane by the spermidine/spermine-N(1)-acetyltransferase and thialysine acetyltransferase.
AID144352Ability to inhibit the deacetylation of [acetyl-3H]-N8-Acetylspermidine deacetylase in rat liver.1989Journal of medicinal chemistry, May, Volume: 32, Issue:5
Design and synthesis of inhibitors of N8-acetylspermidine deacetylase.
AID704420Metabolic stability of the compound assessed as human recombinant APAO-mediated compound degradation at 0.5 to 1 mM after 5 to 60 mins in presence of benzaldehyde2011Journal of medicinal chemistry, Jul-14, Volume: 54, Issue:13
The use of novel C-methylated spermidine derivatives to investigate the regulation of polyamine metabolism.
AID704421Metabolic stability in N1,N11-diethyl-norspermine pretreated human DU145 cells expressing SSAT assessed as accumulation of acetylated derivatives of compound in medium at 100 uM after 48 hrs2011Journal of medicinal chemistry, Jul-14, Volume: 54, Issue:13
The use of novel C-methylated spermidine derivatives to investigate the regulation of polyamine metabolism.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (103)

TimeframeStudies, This Drug (%)All Drugs %
pre-199060 (58.25)18.7374
1990's28 (27.18)18.2507
2000's7 (6.80)29.6817
2010's8 (7.77)24.3611
2020's0 (0.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 9.64

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 weak demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index9.64 (24.57)
Research Supply Index4.67 (2.92)
Research Growth Index4.31 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (9.64)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews2 (1.89%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other104 (98.11%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]