Page last updated: 2024-12-08

n-(1-oxyl-2,2,5,5-tetramethyl-3-pyrrolidinyl)maleimide

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

Description

N-(1-oxyl-2,2,5,5-tetramethyl-3-pyrrolidinyl)maleimide: structure in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID165311
CHEBI ID187890
MeSH IDM0082814

Synonyms (23)

Synonym
AKOS015842152
3-maleimido-proxyl, free radical
3-maleimidoproxyl
5389-27-5
[3-(2,5-dioxo-2,5-dihydro-1h-pyrrol-1-yl)-2,2,5,5-tetramethylpyrrolidin-1-yl]oxidanyl
3-maleimido-2,2,5,5-tetramethyl-1-pyrrolidinyloxy
3-(maleimidomethyl)-2,2,5,5-tetramethyl-1-pyrrolidinyloxyl
3-maleimido-proxyl
proxyl-maleimide
n-(3-(2,2,5,5-tetramethyl-1-pyrrolidinyloxy))maleimide
n-(1-oxyl-2,2,5,5-tetramethyl-3-pyrrolidinyl)maleimide
CHEBI:187890
mal-3
n-1-otpm
mal-5
3-maleimido-1-oxyl-2,2,5,5-tetramethylpyrrolidine
nem-110
1-pyrrolidinyloxy, 3-(2,5-dihydro-2,5-dioxo-1h-pyrrol-1-yl)-2,2,5,5-tetramethyl-
2,2',5,5'-tetramethyl-3-maleimidopyrrolidinyl-n-oxyl
5-msl
3-maleimido-2,2,5,5-tetramethyl-1-pyrrolidinyloxy, free radical
DTXSID50968666
3-(2,5-dihydro-2,5-dioxo-1h-pyrrol-1-yl)-2,2,5,5-tetramethyl-1-pyrrolidinyloxy
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (4)

ClassDescription
aminoxylsRadicals derived from hydroxylamines by removal of the hydrogen atom from the hydroxy group. The synonymous terms nitroxyl radicals and nitroxides erroneously suggest the presence of a nitro group.
maleimidesCompounds containing a cyclic dicarboximide skeleton in which the two carboacyl groups on nitrogen together with the nitrogen itself form a 1H-pyrrole-2,5-dione structure.
pyrrolidinesAny of a class of heterocyclic amines having a saturated five-membered ring.
dicarboximideAn imide in which the two acyl substituents on nitrogen are carboacyl groups.
[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 (34)

TimeframeStudies, This Drug (%)All Drugs %
pre-199021 (61.76)18.7374
1990's5 (14.71)18.2507
2000's3 (8.82)29.6817
2010's5 (14.71)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: 10.84

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 Index10.84 (24.57)
Research Supply Index3.64 (2.92)
Research Growth Index4.48 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (10.84)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies1 (2.70%)4.05%
Observational0 (0.00%)0.25%
Other36 (97.30%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]