Page last updated: 2024-12-07

n-acetylputrescine

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

Description

N-acetylputrescine is a derivative of the polyamine putrescine, formed by the acetylation of the primary amine group. It is synthesized in various organisms, including bacteria, plants, and animals. N-acetylputrescine plays a role in regulating cell growth and differentiation, and it is involved in various biological processes, such as spermidine biosynthesis, polyamine transport, and protection against oxidative stress. N-acetylputrescine has also been studied for its potential therapeutic effects in conditions like cancer and neurodegenerative diseases. Research focuses on understanding its role in polyamine metabolism, its contribution to cellular processes, and its potential as a target for drug development.'

N-acetylputrescine : An N-monoacetylalkane-alpha,omega-diamine that is the N-monoacetyl derivative of putrescine. [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 CID122356
CHEMBL ID81241
CHEBI ID17768
SCHEMBL ID361286
MeSH IDM0086335

Synonyms (31)

Synonym
CHEMBL81241 ,
n-(4-aminobutyl)acetamide
CHEBI:17768 ,
n-acetylputrescine
5699-41-2
C02714
H12005
monoacetylputrescine
putrescine, n-acetyl-
36864054-D6F8-4927-901B-91A60738B493
A4036
n-acetylputrescinehydrochloride
AKOS005215796
n-acetyl-1,4-butanediamine
8ftm5zl5a6 ,
unii-8ftm5zl5a6
acetylputrescine
acetamide, n-(4-aminobutyl)-
bdbm50405938
4-acetylaminobutylamine
SCHEMBL361286
DTXSID80205596
mfcd10024834
NS-01048
Q27102595
n-(4-azanylbutyl)ethanamide
x5a ,
CS-0453679
Z600498842
n1-acetylputrescine
HY-W342604
[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.
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
N-substituted putrescine
N-monoacetylalkane-alpha,omega-diamineAn acetamide obtained by acetylation of one of the amino groups of any alkane-alpha,omega-diamine. AcNHCH2(CH2)nCH2NH2, where n = 0, 1, 2, etc.
[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 (2)

PathwayProteinsCompounds
Arginine and Proline metabolism ( Arginine and Proline metabolism )4255
GABA metabolism (aka GHB)1128

Protein Targets (1)

Inhibition Measurements

ProteinTaxonomyMeasurementAverageMin (ref.)Avg (ref.)Max (ref.)Bioassay(s)
Peroxisomal N(1)-acetyl-spermine/spermidine oxidaseHomo sapiens (human)Ki800.00000.10000.27670.5500AID144352
[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 (2)

Assay IDTitleYearJournalArticle
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.
AID144355In vitro inhibition of N8-Acetylspermidine deacetylase from rat liver cytosol(apparent Ki)1992Journal of medicinal chemistry, Jun-26, Volume: 35, Issue:13
Inhibition of N8-acetylspermidine deacetylase by active-site-directed metal coordinating inhibitors.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (34)

TimeframeStudies, This Drug (%)All Drugs %
pre-199015 (44.12)18.7374
1990's11 (32.35)18.2507
2000's1 (2.94)29.6817
2010's3 (8.82)24.3611
2020's4 (11.76)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 34.21

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 Index34.21 (24.57)
Research Supply Index3.61 (2.92)
Research Growth Index5.18 (4.65)
Search Engine Demand Index39.93 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (34.21)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews1 (2.78%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other35 (97.22%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]