Page last updated: 2024-11-06

dimethyl suberimidate

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

Description

Dimethyl suberimidate, also known as DMS, is a bifunctional cross-linking reagent that forms covalent bonds between primary amines, such as those found in proteins. DMS is synthesized by reacting suberic acid with thionyl chloride to form suberoyl chloride, which is then reacted with dimethylamine. DMS is a popular reagent for cross-linking proteins, as it is relatively stable and reacts readily with primary amines. DMS has been used in a variety of research applications, including the study of protein-protein interactions, the stabilization of protein structures, and the development of new biomaterials. DMS has been shown to be effective in cross-linking proteins, resulting in the formation of stable protein complexes. This property has been exploited in a variety of applications, including the development of new biomaterials, the study of protein-protein interactions, and the stabilization of protein structures. DMS is an important tool for researchers studying protein structure and function, as it allows for the investigation of protein interactions in a controlled manner.'

Dimethyl Suberimidate: The methyl imidoester of suberic acid used to produce cross links in proteins. Each end of the imidoester will react with an amino group in the protein molecule to form an amidine. [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID34750
SCHEMBL ID44286
MeSH IDM0006455

Synonyms (14)

Synonym
DIMETHYLSUBERIMIDATE ,
dimethyl octanediimidate
dimethyl suberimidate
AKOS005173945
unii-x85gk42zu9
29878-26-0
bismethyl suberimidate
octanediimidic acid, dimethyl ester
x85gk42zu9 ,
dimethyl octanebis(imidoate) dihydrochloride
SCHEMBL44286
dimethyl octanediimidoate #
dimethyl octanebis(imidate)
octanediimidic acid, 1,8-dimethyl ester

Research Excerpts

Overview

Dimethyl suberimidate is a bifunctional reagent. It is used for cross-linking the protein components of oligomeric macromolecules.

ExcerptReferenceRelevance
"Dimethyl suberimidate is a bifunctional reagent that is used for cross-linking the protein components of oligomeric macromolecules. "( Dimethyl suberimidate cross-linking of oligo(dT) to DNA-binding proteins.
Dodson, MS,
)
3.02

Effects

ExcerptReferenceRelevance
"Dimethyl suberimidate has been used to study the proximity relations between E. "( [Nearest-neighbor relationships among 50S ribosomal proteins of E. coli].
Barritault, D; Expert-Bezançon, A; Milet, M, 1975
)
1.7

Treatment

Treatment with dimethyl suberimidate, a cross-linking bifunctional agent, showed that Sm1 and Sm2 nucleases of Serratia marcescens B10M1 are polydisperse in solution. Treatment with the agent resulted in a complex consisting of Uf and the associated polypeptides.

ExcerptReferenceRelevance
"Treatment with dimethyl suberimidate, a cross-linking bifunctional agent, showed that Sm1 and Sm2 nucleases of Serratia marcescens B10M1 are polydisperse in solution and consist of monomers and dimers at the level of pH optimal for the enzyme activity. "( [Polydispersity of Serratia marcescens nuclease at optimal pH values].
Benedik, MJ; Filimonova, MN; Leshchinskaia, IB; Urazov, NG,
)
0.48
"Treatment with dimethyl suberimidate, however, results in a cross-linked complex (Mr approximately 82,000) consisting of Uf and the associated polypeptides."( Isolation and characterization of a high molecular weight stable pink form of uteroferrin from uterine secretions and allantoic fluid of pigs.
Baumbach, GA; Bazer, FW; Ketcham, CM; Richardson, DE; Roberts, RM, 1986
)
0.61
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Pathways (1)

PathwayProteinsCompounds
queuosine biosynthesis521

Research

Studies (306)

TimeframeStudies, This Drug (%)All Drugs %
pre-1990217 (70.92)18.7374
1990's72 (23.53)18.2507
2000's11 (3.59)29.6817
2010's6 (1.96)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: 22.72

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 Index22.72 (24.57)
Research Supply Index5.75 (2.92)
Research Growth Index4.15 (4.65)
Search Engine Demand Index24.72 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (22.72)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews2 (0.64%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other310 (99.36%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]