Page last updated: 2024-11-05

methyl malonate

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

Description

methyl malonate: do not confuse with methylmalonate, i.e., malonic acid substituted with a methyl group on C2; structure [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID7943
CHEMBL ID1986332
SCHEMBL ID53913
MeSH IDM0046628

Synonyms (62)

Synonym
EN300-15469
1,3-dimethyl propanedioate
propanedioic acid, dimethyl ester
nsc-620046
nsc620046
NCI60_005924
methyl malonate
dimethyl propanedioate
dimethyl 1,3-propanedioate
einecs 203-597-8
ccris 8981
propanedioic acid,dimethyl ester (malonic acid,dimethyl ester)
dimethyl malonate ,
inchi=1/c5h8o4/c1-8-4(6)3-5(7)9-2/h3h2,1-2h
malonic acid, dimethyl ester
dimethyl malonate, >=99%
dimethyl malonate, 98%
108-59-8
M0030
malonic acid dimethyl ester
AKOS001426594
NCGC00248011-02
NCGC00248011-01
tox21_300375
dtxsid4029145 ,
dtxcid309145
NCGC00254271-01
NCGC00259157-01
cas-108-59-8
tox21_201608
BBL011438
STL146546
ec 203-597-8
propanedioic acid, 1,3-dimethyl ester
unii-em8y79998c
em8y79998c ,
FT-0625086
BP-31034
SCHEMBL53913
methyl malonate [mi]
ch2(coome)2
ch2(co2ch3)2
malonic acid dimethylester
propanedioic acid dimethyl ester
dimethyl ester of malonic acid
CHEMBL1986332
STR00450
CS-0019394
J-002165
F0001-0174
75238-25-4
mfcd00008460
dimethyl malonate, analytical standard
dimethyl malonate, purum, >=96.0% (gc)
D72530
dimethyl malonate, vetec(tm) reagent grade, 98%
malonic acid-dimethyl ester
Q4263082
AMY10014
malonic acid dimethyl ester (1,1,1,7,7,7-d6)
HY-Y1787
Z18909219

Research Excerpts

Overview

Dimethyl malonate (DMM) is a competitive inhibitor of SI dehydrogenase. DMM has been shown to reduce SI accumulation and protect against reperfusion injury.

ExcerptReferenceRelevance
"Dimethyl malonate (DMM) is a competitive inhibitor of SI dehydrogenase, which has been shown to reduce SI accumulation and protect against reperfusion injury."( Dimethyl malonate slows succinate accumulation and preserves cardiac function in a swine model of hemorrhagic shock.
Abdullah, S; Aras, OAZ; Bitonti, N; Cotton-Betteridge, A; Drury, RH; Duchesne, J; Jackson-Weaver, O; Karim, M; Kosowski, EM; Packer, J; Shaheen, F; Taghavi, S; Toraih, E, 2022
)
2

Actions

ExcerptReferenceRelevance
"Methyl malonate was used to inhibit activity of the mitochondrial respiratory chain."( Toxicity of dopamine to striatal neurons in vitro and potentiation of cell death by a mitochondrial inhibitor.
Chesselet, MF; Erecińska, M; McLaughlin, BA; Nelson, D, 1998
)
1.02

Toxicity

ExcerptReferenceRelevance
" Our results suggest that dopamine causes primarily apoptotic death of striatal neurons in culture without damaging cells by an early adverse action on oxidative phosphorylation."( Toxicity of dopamine to striatal neurons in vitro and potentiation of cell death by a mitochondrial inhibitor.
Chesselet, MF; Erecińska, M; McLaughlin, BA; Nelson, D, 1998
)
0.3

Dosage Studied

ExcerptRelevanceReference
" Initially, a curve time- and dose-response to MMA (1-10 mM), MA (1-10 mM) and IP (63-500 μM) was performed."( Ilex paraguariensis Attenuates Changes in Mortality, Behavioral and Biochemical Parameters Associated to Methyl Malonate or Malonate Exposure in Drosophila melanogaster.
Bianchini, MC; Boligon, AA; Carriço, MRS; de Gomes, MG; Hassan, W; Portela, JL; Puntel, RL; Roehrs, R; Soares, FAA, 2019
)
0.73
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Protein Targets (5)

Potency Measurements

ProteinTaxonomyMeasurementAverage (µ)Min (ref.)Avg (ref.)Max (ref.)Bioassay(s)
SMAD family member 2Homo sapiens (human)Potency45.47360.173734.304761.8120AID1346859
SMAD family member 3Homo sapiens (human)Potency45.47360.173734.304761.8120AID1346859
retinoic acid nuclear receptor alpha variant 1Homo sapiens (human)Potency56.70640.003041.611522,387.1992AID1159552; AID1159555
pregnane X nuclear receptorHomo sapiens (human)Potency47.63860.005428.02631,258.9301AID1346982
peroxisome proliferator activated receptor gammaHomo sapiens (human)Potency64.23320.001019.414170.9645AID743094
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (56)

TimeframeStudies, This Drug (%)All Drugs %
pre-199013 (23.21)18.7374
1990's10 (17.86)18.2507
2000's13 (23.21)29.6817
2010's14 (25.00)24.3611
2020's6 (10.71)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 72.41

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 very strong demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index72.41 (24.57)
Research Supply Index4.08 (2.92)
Research Growth Index4.64 (4.65)
Search Engine Demand Index122.12 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (72.41)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials1 (1.75%)5.53%
Reviews1 (1.75%)6.00%
Case Studies4 (7.02%)4.05%
Observational0 (0.00%)0.25%
Other51 (89.47%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]