Page last updated: 2024-11-05

5-methyl-2-furfural

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

Description

5-Methyl-2-furfural (5-MF) is a heterocyclic organic compound. It is a colorless liquid that is soluble in water, ethanol, and ether. 5-MF is found in a wide variety of food products, including coffee, honey, and baked goods. It is produced during the thermal processing of food, such as roasting, baking, and frying. 5-MF is a potent antioxidant that has been shown to protect against oxidative damage in cells. It has also been shown to have anti-inflammatory and anti-cancer properties. 5-MF is of interest to researchers because of its potential health benefits. It is also being studied for its use as a biofuel and as a precursor to other valuable chemicals.'

5-methyl-2-furfural: RN given refers to cpd with locants as specified [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID12097
CHEMBL ID2230304
CHEBI ID2091
SCHEMBL ID51606
SCHEMBL ID11096252
MeSH IDM0138508

Synonyms (82)

Synonym
5-methyl-furan-2-carbaldehyde
2-furaldehyde, 5-methyl-
2-furancarboxaldehyde, 5-methyl-
5-methylfurfuraldehyde
5-methylfurfural
5-methyl-2-furancarboxaldehyde
2-methyl-5-formylfuran
ai3-36591
ccris 2921
einecs 210-622-6
brn 0106895
2-formyl-5-methylfuran
5-methyl-2-furfuraldehyde
5-methylfuran-2-carbaldehyde
fema no. 2702
5-methylfuran-2-al
5-methyl furfural
5-methylfuran-2-aldehyde
5-methyl-2-furaldehyde
620-02-0
5-methyl-2-furfural
5-methylfurfural, >=98%, fg
5-methylfurfural, reagentplus(r), 99%
inchi=1/c6h6o2/c1-5-2-3-6(4-7)8-5/h2-4h,1h3
oudfnzmqxziljd-uhfffaoysa-
M0254
AKOS000119751
A833524
QSPL 010
S9381
4482bzc72d ,
5-17-09-00404 (beilstein handbook reference)
unii-4482bzc72d
FT-0620652
SCHEMBL51606
CHEMBL2230304
chebi:2091 ,
5-methyl-2-furfurylaldehyde
methyl furfural, 5-
methyl-5-furaldehyde
2-formyl-5-methyltetrahydrofuran
5-methyl furfural [fcc]
5-methyl furfural [fhfi]
5-methyl-furfural
5-methyl-2-furancarbaldehyde
5-methyl furfuraldehyde
5-methyl furaldehyde
2-methylfuran-5-aldehyde
5-methylfuran-2-carboxaldehyde
5-methylfuran-2 carbaldehyde
SCHEMBL11096252
DTXSID1060714
J-640041
STR02593
AC-34339
Q-100716
5-methyifurfural
5-methyl-2-furanaldehyde
furfural, 5-methyl-
HY-Y0543
F2190-0577
5-methylfurfural, analytical reference material
mfcd00003232
GEO-01838
5-methylfurfural, vetec(tm) reagent grade, 98%
5-methyl-2-furfural; 5-methylfuran-2-carbaldehyde
BP-30242
5-methyl-2-furancarboxyaldehyde
methyl-5-furfural
fema 2702
alpha-methylfurfural
CS-W020103
SY001535
Z56899216
Q22830264
AMY23296
5-methylfuran-2-carbaldehyde;5-methyl-2-furaldehyde
BCP31055
CCG-266047
AC7802
PD087963
EN300-17263
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (4)

RoleDescription
Maillard reaction productAny thermal degradation product obtained as a result of a chemical reaction between an amino acid and a reducing sugar (Maillard reaction, a non-enzymatic browning procedure that usually imparts flavour to starch-based food products).
human metaboliteAny mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens).
EC 2.2.1.6 (acetolactate synthase) inhibitorAn EC 2.2.1.* (transketolase/transaldolase) inhibitor that interferes with the action of acetolactate synthase (EC 2.2.1.6).
flavouring agentA food additive that is used to added improve the taste or odour of a food.
[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
furansCompounds containing at least one furan ring.
aldehydeA compound RC(=O)H, in which a carbonyl group is bonded to one hydrogen atom and to one R group.
[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]

Bioassays (1)

Assay IDTitleYearJournalArticle
AID1083150Nematotoxic activity against Meloidogyne incognita (root-knot nematode)2012Journal of agricultural and food chemistry, Nov-28, Volume: 60, Issue:47
Nematotoxic phenolic compounds from Melia azedarach against Meloidogyne incognita.
[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-19902 (5.88)18.7374
1990's4 (11.76)18.2507
2000's7 (20.59)29.6817
2010's12 (35.29)24.3611
2020's9 (26.47)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 26.17

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 moderate demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index26.17 (24.57)
Research Supply Index3.56 (2.92)
Research Growth Index5.05 (4.65)
Search Engine Demand Index29.35 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (26.17)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews1 (2.94%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other33 (97.06%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]