Page last updated: 2024-11-06

n,n'-4-phenylenedimaleimide

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

n,n'-4-phenylenedimaleimide is a bismaleimide monomer, a type of thermosetting resin known for its high thermal stability, good mechanical properties, and excellent electrical insulation. It is typically synthesized through a reaction of 4-phenylenediamine with maleic anhydride. This compound is of interest due to its potential applications in various fields, including aerospace, electronics, and automotive industries. Research on n,n'-4-phenylenedimaleimide focuses on improving its processability, enhancing its thermal and mechanical properties, and exploring its use in advanced composite materials.'

Cross-References

ID SourceID
PubMed CID76765
CHEMBL ID576594
SCHEMBL ID95324
MeSH IDM0057544

Synonyms (41)

Synonym
n,n'-p-phenylenedimaleimide
n,n'-4-phenylenedimaleimide
einecs 221-910-6
unii-bec7p1e6j1
bec7p1e6j1 ,
nsc 81257
dimaleimide, n,n'-p-phenylene-
nsc-81257
nsc81257
3278-31-7
n,n'-(1,4-phenylene)dimaleimide, 97%
1,1'-(1,4-phenylene)bis(1h-pyrrole-2,5-dione)
phenyl-1,4-bismaleimide
CHEMBL576594 ,
n,n'-1,4-bismaleimidobenzene
n,n'-1,4-phenylenedimaleimide
n,n'-1,4-phenylenebismaleimide
P0778
bdbm50300348
1-[4-(2,5-dioxopyrrol-1-yl)phenyl]pyrrole-2,5-dione
AKOS004115368
n,n'-(1,4-phenylene)dimaleimide
FT-0629403
p-phenylene dimaleimide
1h-pyrrole-2,5-dione, 1,1'-(1,4-phenylene)bis-
1,1'-benzene-1,4-diylbis(1h-pyrrole-2,5-dione)
SCHEMBL95324
AQGZJQNZNONGKY-UHFFFAOYSA-N
n,n'-p-phenylene bismaleimide
1,4-bis(maleimido)benzene
n,n-1,4-phenylenedimaleimide
DTXSID70186446
mfcd00005505
AS-59470
1-[4-(2,5-dioxo-2,5-dihydro-1h-pyrrol-1-yl)phenyl]-2,5-dihydro-1h-pyrrole-2,5-dione
n,n'-1,4-phenylenedimaleimide, >/=98%
J-018875
1,4-phenylene-bis-maleimide
Q27274616
D92013
1,3-phenylene bismalemide
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Protein Targets (2)

Inhibition Measurements

ProteinTaxonomyMeasurementAverageMin (ref.)Avg (ref.)Max (ref.)Bioassay(s)
Fatty-acid amide hydrolase 1Homo sapiens (human)IC50 (µMol)13.49000.00020.59827.0000AID439745
Monoglyceride lipaseHomo sapiens (human)IC50 (µMol)2.22000.00091.126810.0000AID439744
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Biological Processes (13)

Processvia Protein(s)Taxonomy
fatty acid catabolic processFatty-acid amide hydrolase 1Homo sapiens (human)
arachidonic acid metabolic processFatty-acid amide hydrolase 1Homo sapiens (human)
positive regulation of vasoconstrictionFatty-acid amide hydrolase 1Homo sapiens (human)
monoacylglycerol catabolic processFatty-acid amide hydrolase 1Homo sapiens (human)
lipid metabolic processMonoglyceride lipaseHomo sapiens (human)
fatty acid biosynthetic processMonoglyceride lipaseHomo sapiens (human)
inflammatory responseMonoglyceride lipaseHomo sapiens (human)
regulation of signal transductionMonoglyceride lipaseHomo sapiens (human)
arachidonic acid metabolic processMonoglyceride lipaseHomo sapiens (human)
triglyceride catabolic processMonoglyceride lipaseHomo sapiens (human)
acylglycerol catabolic processMonoglyceride lipaseHomo sapiens (human)
regulation of inflammatory responseMonoglyceride lipaseHomo sapiens (human)
regulation of sensory perception of painMonoglyceride lipaseHomo sapiens (human)
monoacylglycerol catabolic processMonoglyceride lipaseHomo sapiens (human)
regulation of endocannabinoid signaling pathwayMonoglyceride lipaseHomo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Molecular Functions (8)

Processvia Protein(s)Taxonomy
protein bindingFatty-acid amide hydrolase 1Homo sapiens (human)
phospholipid bindingFatty-acid amide hydrolase 1Homo sapiens (human)
fatty acid amide hydrolase activityFatty-acid amide hydrolase 1Homo sapiens (human)
identical protein bindingFatty-acid amide hydrolase 1Homo sapiens (human)
acylglycerol lipase activityFatty-acid amide hydrolase 1Homo sapiens (human)
amidase activityFatty-acid amide hydrolase 1Homo sapiens (human)
lysophospholipase activityMonoglyceride lipaseHomo sapiens (human)
protein bindingMonoglyceride lipaseHomo sapiens (human)
protein homodimerization activityMonoglyceride lipaseHomo sapiens (human)
acylglycerol lipase activityMonoglyceride lipaseHomo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Ceullar Components (6)

Processvia Protein(s)Taxonomy
endoplasmic reticulum membraneFatty-acid amide hydrolase 1Homo sapiens (human)
cytoskeletonFatty-acid amide hydrolase 1Homo sapiens (human)
organelle membraneFatty-acid amide hydrolase 1Homo sapiens (human)
endoplasmic reticulum membraneMonoglyceride lipaseHomo sapiens (human)
cytosolMonoglyceride lipaseHomo sapiens (human)
plasma membraneMonoglyceride lipaseHomo sapiens (human)
membraneMonoglyceride lipaseHomo sapiens (human)
membraneMonoglyceride lipaseHomo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Bioassays (4)

Assay IDTitleYearJournalArticle
AID439743Selectivity ratio of IC50 for human FAAH to IC50 for human MGL2009Journal of medicinal chemistry, Dec-10, Volume: 52, Issue:23
Synthesis and in vitro evaluation of N-substituted maleimide derivatives as selective monoglyceride lipase inhibitors.
AID439747Ratio of N-phenylmaleimide IC50 to compound IC50 for human recombinant MGL2009Journal of medicinal chemistry, Dec-10, Volume: 52, Issue:23
Synthesis and in vitro evaluation of N-substituted maleimide derivatives as selective monoglyceride lipase inhibitors.
AID439745Displacement of [3H]ethanolamine from human recombinant FAAH by liquid scintillation counting2009Journal of medicinal chemistry, Dec-10, Volume: 52, Issue:23
Synthesis and in vitro evaluation of N-substituted maleimide derivatives as selective monoglyceride lipase inhibitors.
AID439744Displacement of [3H]2-OG from human MGL by liquid scintillation counting2009Journal of medicinal chemistry, Dec-10, Volume: 52, Issue:23
Synthesis and in vitro evaluation of N-substituted maleimide derivatives as selective monoglyceride lipase inhibitors.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (55)

TimeframeStudies, This Drug (%)All Drugs %
pre-199021 (38.18)18.7374
1990's20 (36.36)18.2507
2000's11 (20.00)29.6817
2010's3 (5.45)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: 10.17

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 Index10.17 (24.57)
Research Supply Index4.03 (2.92)
Research Growth Index4.20 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (10.17)

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%
Other55 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]