Page last updated: 2024-12-05

furaldehyde

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

Description

Furaldehyde, also known as furfural, is a heterocyclic organic compound with the formula C4H3OCHO. It is a colorless liquid that is produced from the dehydration of pentoses, such as xylose and arabinose, which are found in plant materials like corncobs, oat hulls, and rice hulls. Furaldehyde is used as a solvent, a flavoring agent, and a precursor to other chemicals. It is also used in the production of resins, polymers, and pharmaceuticals. Furaldehyde has a wide range of effects on human health and the environment. It is a known irritant to the skin, eyes, and respiratory system. It can also be toxic if ingested or inhaled in large amounts. Furaldehyde is studied for its potential use in the production of biofuels and other renewable energy sources. Its importance is further demonstrated by its use as an indicator of food quality and freshness.'

Furaldehyde: A heterocyclic compound consisting of a furan where the hydrogen at position 2 is substituted by a formyl group. [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

furfural : An aldehyde that is furan with the hydrogen at position 2 substituted by a formyl group. [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]

Cross-References

ID SourceID
PubMed CID7362
CHEMBL ID189362
CHEBI ID34768
MeSH IDM0008897

Synonyms (134)

Synonym
BIDD:ER0698
ccris 1044
hsdb 542
rcra waste number u125
fema no. 2489
2-furylcarboxaldehyde
2-formylofuran [polish]
epa pesticide chemical code 043301
quakeral
alpha-furole
2-furylmethanal
un1199
2-formyl furan
alpha-furfuraldehyde
2-furil-metanale [italian]
2-furankarbaldehyd [czech]
fufural
furfural (natural)
furfurale [italian]
einecs 202-627-7
furyl-methanal
rcra waste no. u125
ai3-04466
nsc 8841
brn 0105755
u1199
caswell no. 466
2-furylaldehyde
pyromucic aldehyde
2-furanaldehyde
2-furaldehyde
furfurole
furfural
2-furfural
wln: t5oj bvh
furancarbonal
2-furancarbonal
furaldehyde
.alpha.-furole
furfuraldehyde
98-01-1
furole
furfurylaldehyde
2-furil-metanale
fural
2-furyl-methanal
furale
2-furfuraldehyde
nsc8841
furol
2-furancarboxaldehyde
furfurale
nsc-8841
2-formylfuran
nci-c56177
inchi=1/c5h4o2/c6-4-5-2-1-3-7-5/h1-4
NCGC00091328-01
furfural, >=98%, fcc, fg
furfural, natural, >=98%, fcc, fg
furfural, acs reagent, 99%
furfural, 99%
AKOS000118907
furan-2-carbaldehyde
CHEMBL189362
chebi:34768 ,
F0073
A845786
QSPL 006
NCGC00091328-02
NCGC00091328-04
NCGC00091328-03
QSPL 102
tox21_300170
NCGC00259740-01
tox21_202191
NCGC00253954-01
dtxsid1020647 ,
cas-98-01-1
dtxcid50647
tox21_111114
furan-2-carboxaldehyde
STL283124
unii-dj1hgi319p
dj1hgi319p ,
furaldehydes
furaldehydes [un1199] [poison]
2-formylofuran
ec 202-627-7
5-17-09-00292 (beilstein handbook reference)
2-furankarbaldehyd
FT-0612462
BP-31002
AM81812
furfural [iarc]
ascorbic acid impurity a [ep impurity]
furfural [fcc]
furfural [inci]
furfural [mi]
furfural [hsdb]
furfural [fhfi]
2-furanal
furan-2 carbaldehyde
2-furan-carboxaldehyde
furan-2-aldehyde
2-furancarbaldehyde
qo furfural
STR00358
mfcd00003229
F1294-0048
furfural, saj first grade, >=99.0%
furfural, analytical reference material
bdbm50486229
furfural acs grade
2-furanocarboxyaldehyde
furfural, for synthesis, 98.0%
2-furylaldehyde xypropane
2-furaldehyde, 8ci
a-furfuraldehyde
2-furancarboxyaldehyde
a-furole
furfuralu
fema 2489
CS-0015696
Q412429
furfural 100 microg/ml in acetonitrile
furfural-d4
furfural; furfuraldehyde; furfurol; 2-furaldehyde; 2-furancarboxaldehyde; furan-2-carboxaldehyde
furan-2-carbaldehyde (furfural)
EN300-18110
fural/pyromucic aldehyde
furfuraldehydes
furfural (iarc)
alpha-furaldehyde
usepa/opp pesticide code: 043301

Research Excerpts

Toxicity

ExcerptReferenceRelevance
" cerevisiae through a variety of toxic molecular mechanisms, predominantly via damaging macromolecules and hampering the production of targeted compounds."( In-depth understanding of molecular mechanisms of aldehyde toxicity to engineer robust Saccharomyces cerevisiae.
Jayakody, LN; Jin, YS, 2021
)
0.62

Compound-Compound Interactions

ExcerptReferenceRelevance
" Honey in combination with vacuum impregnating operation may have a great potential for developing high-quality fresh-cut fruits."( Honey in combination with vacuum impregnation to prevent enzymatic browning of fresh-cut apples.
Jeon, M; Zhao, Y, 2005
)
0.33
"A novel conversion process using steam explosion combined with enzymatic digestibility was exploited to increase sugar yield."( Xylose production from corn stover biomass by steam explosion combined with enzymatic digestibility.
Chen, HZ; Liu, ZH, 2015
)
0.42
"The IPL pretreatment combined with controlled temperature and humidity for convection drying could be a suitable method to improve the quality of dried shiitake mushrooms."( Intensive pulsed light pretreatment combined with controlled temperature and humidity for convection drying to reduce browning and improve quality of dried shiitake mushrooms.
Ma, H; S Mujumdar, A; Sun, Y; Wahia, H; Yagoub, AEA; Zhang, J; Zhou, C, 2021
)
0.62
" To achieve the reutilization of the condensate, the ozonation combined with ion-exchange method was used."( Exploring the resourcing technology of condensate using ozonation combined with ion-exchange in ethanol fermentation.
Li, Z; Sheng, X; Zhang, J, 2022
)
0.72

Bioavailability

ExcerptReferenceRelevance
" The criteria on which such regulations are based include biological and chemical degradability, bioavailability (accumulation) and toxicity, the latter manifesting itself in a reduced ability of organisms to survive and reproduce."( The role of mutagenicity testing in the ecotoxicological evaluation of industrial discharges into the aquatic environment.
de Kreuk, JF; de Raat, WK; Hanstveit, AO, 1985
)
0.27
"During processing of pet food, the Maillard reaction occurs, which reduces the bioavailability of essential amino acids such as lysine and results in the formation of advanced Maillard reaction products (MRPs)."( Quantitation of Maillard reaction products in commercially available pet foods.
Alexander, L; Bosch, G; Hendriks, WH; van der Poel, AF; van Rooijen, C; Wierenga, PA, 2014
)
0.4
"The ATP-binding cassette transporter P-glycoprotein (P-gp) is known to limit both brain penetration and oral bioavailability of many chemotherapy drugs."( A High-Throughput Screen of a Library of Therapeutics Identifies Cytotoxic Substrates of P-glycoprotein.
Ambudkar, SV; Brimacombe, KR; Chen, L; Gottesman, MM; Guha, R; Hall, MD; Klumpp-Thomas, C; Lee, OW; Lee, TD; Lusvarghi, S; Robey, RW; Shen, M; Tebase, BG, 2019
)
0.51

Dosage Studied

ExcerptRelevanceReference
" Furfural was dosed by gavage at levels of 0 (control), 50, 175 and 320 mg/kg to male and female mice and 0, 5, 16."( Lack of effect of furfural on unscheduled DNA synthesis in the in vivo rat and mouse hepatocyte DNA repair assays and in precision-cut human liver slices.
Adams, TB; Beamand, JA; Edwards, AJ; Lake, BG; Phillips, BJ; Price, RJ; Renwick, AB, 2001
)
0.31
" Caged bee studies were conducted to evaluate the HMF dose-response effect on bee mortality."( Formation of hydroxymethylfurfural in domestic high-fructose corn syrup and its toxicity to the honey bee (Apis mellifera).
Cornett, C; Deeby, T; Dufault, R; Eggleston, G; LeBlanc, BW; Sammataro, D; St Cyr, E, 2009
)
0.35
" The impurity was identified as 5-hydroxymethyl furfural, which was a degradation product of lactose, one of the excipients used in the formulation of this dosage form."( A multidisciplinary approach to identify a degradation product in a pharmaceutical dosage form.
Guan, J; Lin, M; Pan, C, 2011
)
0.37
" The effects of catalyst dosage (mole ratio of catalyst to glucose units in the feedstock) and reaction temperature on HMF yields were investigated to obtain optimal process conditions."( Catalytic hydrolysis of lignocellulosic biomass into 5-hydroxymethylfurfural in ionic liquid.
Wang, P; Wang, S; Yu, H; Zhan, S, 2011
)
0.37
" Conversely, high catalyst dosage mainly accelerated the conversion of glucose to methyl levulinate."( Reaction pathways of glucose during esterification: effects of reaction parameters on the formation of humin type polymers.
Hu, X; Larcher, A; Li, CZ; Lievens, C, 2011
)
0.37
" At a dosage of 250 mg/kg, most animals died after 5-11 days due to massive damage to proximal tubules."( Toxicity studies with 5-hydroxymethylfurfural and its metabolite 5-sulphooxymethylfurfural in wild-type mice and transgenic mice expressing human sulphotransferases 1A1 and 1A2.
Bauer-Marinovic, M; Florian, S; Glatt, H; Taugner, F, 2012
)
0.38
"It revealed that the high and medium dosage of 5-HMF could increase the activity of rat hippocampal."( [Effect of 5-hydroxymethyl furfural on BCL-2 and NF-kappaB gene expression of apoptotic rat hippocampal neurons injured by H2O2].
Ding, X; Gu, H; Jiang, HY; Jiang, YB; Wang, MY; Xu, DQ; Yu, JT; Zhan, Z; Zhao, FM, 2011
)
0.37
"To detect 5-HMF from rabbit ncurolymph after given different dosage of Cornus officinalis via intragastric administration by HPLC and UPLC-MS."( [HPLC and UPLC-MS detection of 5-HMF from rabbit ncurolymph after treated with Cornus officinalis].
Gu, H; Liu, R; Liu, T; Liu, XF; Wang, MY; Zhan, Z, 2013
)
0.39
"Rabbit ncurolymph was cramped out three days after given low, medium, and high dosage of Cornus officinalis."( [HPLC and UPLC-MS detection of 5-HMF from rabbit ncurolymph after treated with Cornus officinalis].
Gu, H; Liu, R; Liu, T; Liu, XF; Wang, MY; Zhan, Z, 2013
)
0.39
" Various reaction parameters such as reaction time, reaction temperature, solvent and catalyst dosage were investigated in detail."( Efficient conversion of cellulose into biofuel precursor 5-hydroxymethylfurfural in dimethyl sulfoxide-ionic liquid mixtures.
Fang, Z; Liu, B; Wang, Y; Xiao, S; Zhang, Z, 2014
)
0.4
") approach to map, in parallel, the effect of increased dosage for >10(5) different fragments of the Escherichia coli genome onto furfural tolerance (furfural is a key toxin of lignocellulosic hydrolysate)."( Genome-wide mapping of furfural tolerance genes in Escherichia coli.
Gill, RT; Glebes, TY; Reeder, PJ; Sandoval, NR; Schilling, KD; Zhang, M, 2014
)
0.4
"2% dosage with negligible HDSs loss."( Separation and purification of hemicellulose-derived saccharides from wood hydrolysate by combined process.
Fu, Y; Jiang, J; Qin, M; Wang, X; Wang, Z; Zhuang, J, 2015
)
0.42
" This investigation focused on effects of various reaction conditions including solvent, acid catalyst, reaction temperature, residence time, water concentration, xylose loading and catalyst dosage on the dehydration of xylose to furfural."( Conversion of corn stalk into furfural using a novel heterogeneous strong acid catalyst in γ-valerolactone.
Chang, HM; Du, Z; Jameel, H; Li, W; Ma, L; Wu, H; Xu, Z, 2015
)
0.42
" The influence of the reaction time, temperature and dosage of catalyst on xylose dehydration were also investigated."( Catalytic conversion of xylose and corn stalk into furfural over carbon solid acid catalyst in γ-valerolactone.
Chang, HM; Jameel, H; Li, W; Liu, Q; Ma, L; Ma, Q; Xu, Z; Zhang, T, 2016
)
0.43
" As the pretreatment dosage of GL-H2O2 on FR increased, the proportion of lignocellulosic substrates was enhanced in the SSF of the substrate mixture of CR and FR as compared with untreated FR."( Ethanol production from a biomass mixture of furfural residues with green liquor-peroxide saccarified cassava liquid.
Ji, L; Jiang, J; Zhang, W; Zhao, P; Zheng, T, 2016
)
0.43
"1 M) was tested, obtaining that the dose-response curve is fitted by the Langmuir adsorption isotherm."( A MIP-based low-cost electrochemical sensor for 2-furaldehyde detection in beverages.
Alberti, G; Biesuz, R; Marchetti, S; Merli, D; Milanese, C; Pesavento, M, 2021
)
0.87
" The influences of reaction temperature, reaction time, catalyst dosage on the yield of 5-hydroxymethylfurfural (5-HFM) were investigated."( Novel solid acid catalyst for the production of 5-hydroxymethylfurfural with fructose dehydration.
Liu, S; Shang, D; Wang, H; Wu, J, 2022
)
0.72
" The results revealed that an increased glycylglycine dosage level enhanced both the conversion of XGG-ARP to XGG-CP and the conversion of XGG-CP to 3-deoxyosone."( Temperature-Dependent Catalysis of Glycylglycine on Its Amadori Compound Degradation to Deoxyosone.
Cui, H; Hayat, K; Ho, CT; Ma, M; Wang, Z; Zhang, X, 2022
)
0.72
"1%) at 35 °C for 12 h through in situ removal of the amino transfer by-products of the amine donor, greatly reducing amine donor dosage (from D-Ala/5-HMF = 16/1 to D-Ala/5-HMF = 2/1, mol/mol) and improving the productivity of HMFA (0."( Efficient production of hydroxymethyl-2-furfurylamine by chemoenzymatic cascade catalysis of bread waste in a sustainable approach.
Chai, H; He, YC; Li, Q; Ma, C; Wu, C, 2023
)
0.91
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (2)

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).
metaboliteAny intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
[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]

Pathways (1)

PathwayProteinsCompounds
furfural degradation517

Protein Targets (13)

Potency Measurements

ProteinTaxonomyMeasurementAverage (µ)Min (ref.)Avg (ref.)Max (ref.)Bioassay(s)
GLI family zinc finger 3Homo sapiens (human)Potency66.29430.000714.592883.7951AID1259369
AR proteinHomo sapiens (human)Potency56.82420.000221.22318,912.5098AID1259243; AID1259247; AID1259381; AID743040; AID743054
aldehyde dehydrogenase 1 family, member A1Homo sapiens (human)Potency28.18380.011212.4002100.0000AID1030
retinoic acid nuclear receptor alpha variant 1Homo sapiens (human)Potency68.48460.003041.611522,387.1992AID1159552; AID1159555
pregnane X nuclear receptorHomo sapiens (human)Potency59.08480.005428.02631,258.9301AID1346982
estrogen nuclear receptor alphaHomo sapiens (human)Potency0.04900.000229.305416,493.5996AID743075
peroxisome proliferator-activated receptor deltaHomo sapiens (human)Potency0.06310.001024.504861.6448AID588535
activating transcription factor 6Homo sapiens (human)Potency18.83980.143427.612159.8106AID1159516
Caspase-7Cricetulus griseus (Chinese hamster)Potency66.29430.006723.496068.5896AID1346980
caspase-3Cricetulus griseus (Chinese hamster)Potency66.29430.006723.496068.5896AID1346980
thyroid hormone receptor beta isoform 2Rattus norvegicus (Norway rat)Potency13.33320.000323.4451159.6830AID743065
Nuclear receptor ROR-gammaHomo sapiens (human)Potency8.41270.026622.448266.8242AID651802
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Inhibition Measurements

ProteinTaxonomyMeasurementAverageMin (ref.)Avg (ref.)Max (ref.)Bioassay(s)
Polyphenol oxidase 2Agaricus bisporusIC50 (µMol)43.00000.03403.987110.0000AID1082239
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Biological Processes (13)

Processvia Protein(s)Taxonomy
negative regulation of transcription by RNA polymerase IINuclear receptor ROR-gammaHomo sapiens (human)
xenobiotic metabolic processNuclear receptor ROR-gammaHomo sapiens (human)
regulation of glucose metabolic processNuclear receptor ROR-gammaHomo sapiens (human)
regulation of steroid metabolic processNuclear receptor ROR-gammaHomo sapiens (human)
intracellular receptor signaling pathwayNuclear receptor ROR-gammaHomo sapiens (human)
circadian regulation of gene expressionNuclear receptor ROR-gammaHomo sapiens (human)
cellular response to sterolNuclear receptor ROR-gammaHomo sapiens (human)
positive regulation of circadian rhythmNuclear receptor ROR-gammaHomo sapiens (human)
regulation of fat cell differentiationNuclear receptor ROR-gammaHomo sapiens (human)
positive regulation of DNA-templated transcriptionNuclear receptor ROR-gammaHomo sapiens (human)
adipose tissue developmentNuclear receptor ROR-gammaHomo sapiens (human)
T-helper 17 cell differentiationNuclear receptor ROR-gammaHomo sapiens (human)
regulation of transcription by RNA polymerase IINuclear receptor ROR-gammaHomo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Molecular Functions (10)

Processvia Protein(s)Taxonomy
RNA polymerase II cis-regulatory region sequence-specific DNA bindingNuclear receptor ROR-gammaHomo sapiens (human)
DNA-binding transcription factor activity, RNA polymerase II-specificNuclear receptor ROR-gammaHomo sapiens (human)
DNA-binding transcription repressor activity, RNA polymerase II-specificNuclear receptor ROR-gammaHomo sapiens (human)
DNA-binding transcription factor activityNuclear receptor ROR-gammaHomo sapiens (human)
protein bindingNuclear receptor ROR-gammaHomo sapiens (human)
oxysterol bindingNuclear receptor ROR-gammaHomo sapiens (human)
zinc ion bindingNuclear receptor ROR-gammaHomo sapiens (human)
ligand-activated transcription factor activityNuclear receptor ROR-gammaHomo sapiens (human)
sequence-specific double-stranded DNA bindingNuclear receptor ROR-gammaHomo sapiens (human)
nuclear receptor activityNuclear receptor ROR-gammaHomo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Ceullar Components (4)

Processvia Protein(s)Taxonomy
nucleusNuclear receptor ROR-gammaHomo sapiens (human)
nucleoplasmNuclear receptor ROR-gammaHomo sapiens (human)
nuclear bodyNuclear receptor ROR-gammaHomo sapiens (human)
chromatinNuclear receptor ROR-gammaHomo sapiens (human)
nucleusNuclear receptor ROR-gammaHomo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Bioassays (32)

Assay IDTitleYearJournalArticle
AID504749qHTS profiling for inhibitors of Plasmodium falciparum proliferation2011Science (New York, N.Y.), Aug-05, Volume: 333, Issue:6043
Chemical genomic profiling for antimalarial therapies, response signatures, and molecular targets.
AID1346986P-glycoprotein substrates identified in KB-3-1 adenocarcinoma cell line, qHTS therapeutic library screen2019Molecular pharmacology, 11, Volume: 96, Issue:5
A High-Throughput Screen of a Library of Therapeutics Identifies Cytotoxic Substrates of P-glycoprotein.
AID1296008Cytotoxic Profiling of Annotated Libraries Using Quantitative High-Throughput Screening2020SLAS discovery : advancing life sciences R & D, 01, Volume: 25, Issue:1
Cytotoxic Profiling of Annotated and Diverse Chemical Libraries Using Quantitative High-Throughput Screening.
AID1346987P-glycoprotein substrates identified in KB-8-5-11 adenocarcinoma cell line, qHTS therapeutic library screen2019Molecular pharmacology, 11, Volume: 96, Issue:5
A High-Throughput Screen of a Library of Therapeutics Identifies Cytotoxic Substrates of P-glycoprotein.
AID1082761Nematicidal Activity against Meloidogyne javanica (root-knot nematode) assessed as death/paralysis of nematodes at 1 day after immersion in test solution2012Journal of agricultural and food chemistry, Feb-01, Volume: 60, Issue:4
Nematicidal activity of (E,E)-2,4-decadienal and (E)-2-decenal from Ailanthus altissima against Meloidogyne javanica.
AID1081752Nematicidal activity against Meloidogyne incognita J2 (root-knot nematode) assessed as paralysis measured after 1 day at 28 degC by fumigant assay2010Journal of agricultural and food chemistry, Nov-10, Volume: 58, Issue:21
nematicidal carboxylic acids and aldehydes from Melia azedarach fruits.
AID1113017Nematicidal activity against second-stage juveniles of Meloidogyne incognita (root-knot nematode) after 1 day by inverted microscopic analysis2013Journal of agricultural and food chemistry, Feb-27, Volume: 61, Issue:8
Potent nematicidal activity of phthalaldehyde, salicylaldehyde, and cinnamic aldehyde against Meloidogyne incognita.
AID1081754Nematicidal activity against Meloidogyne incognita J2 (root-knot nematode) assessed as paralysis measured after 1 day at 28 degC2010Journal of agricultural and food chemistry, Nov-10, Volume: 58, Issue:21
nematicidal carboxylic acids and aldehydes from Melia azedarach fruits.
AID1113018Nematicidal activity against second-stage juveniles of Meloidogyne incognita (root-knot nematode) after 1 hr by inverted microscopic analysis2013Journal of agricultural and food chemistry, Feb-27, Volume: 61, Issue:8
Potent nematicidal activity of phthalaldehyde, salicylaldehyde, and cinnamic aldehyde against Meloidogyne incognita.
AID1082760Nematicidal Activity against Meloidogyne javanica (root-knot nematode) assessed as death/paralysis of nematodes at 1 hr after immersion in test solution2012Journal of agricultural and food chemistry, Feb-01, Volume: 60, Issue:4
Nematicidal activity of (E,E)-2,4-decadienal and (E)-2-decenal from Ailanthus altissima against Meloidogyne javanica.
AID1082238Inhibition of Oryctolagus cuniculus (rabbit) AOX in liver cytosol2011Journal of agricultural and food chemistry, May-11, Volume: 59, Issue:9
Neonicotinoid insecticides: oxidative stress in planta and metallo-oxidase inhibition.
AID251934Percent inhibition of sickling of sickle red blood (SS) cells under 4% oxygen was evaluated at 2 mM concentration2004Journal of medicinal chemistry, Sep-09, Volume: 47, Issue:19
Structural basis for the potent antisickling effect of a novel class of five-membered heterocyclic aldehydic compounds.
AID1082232Inhibition of xanthine oxidase at IC50 concentration2011Journal of agricultural and food chemistry, May-11, Volume: 59, Issue:9
Neonicotinoid insecticides: oxidative stress in planta and metallo-oxidase inhibition.
AID1082889Nematicidal activity against Meloidogyne incognita (root-knot nematode) juveniles J2 assessed as paralysis after 1 hr2012Journal of agricultural and food chemistry, Aug-01, Volume: 60, Issue:30
Nematicidal activity of 2-thiophenecarboxaldehyde and methylisothiocyanate from caper (Capparis spinosa) against Meloidogyne incognita.
AID251933Percent inhibition of sickling of sickle red blood (SS) cells under 4% oxygen was evaluated at 1 mM concentration2004Journal of medicinal chemistry, Sep-09, Volume: 47, Issue:19
Structural basis for the potent antisickling effect of a novel class of five-membered heterocyclic aldehydic compounds.
AID1167300Antioxidant activity assessed as DPPH radical scavenging activity incubated at room temperature for 20 mins by UV-visible spectrophotometry2014Bioorganic & medicinal chemistry letters, Nov-01, Volume: 24, Issue:21
Design, synthesis and exploring the quantitative structure-activity relationship of some antioxidant flavonoid analogues.
AID281491Inhibition of SARS coronavirus His-3C-like protease at 100 uM2007Journal of medicinal chemistry, Apr-19, Volume: 50, Issue:8
Design, synthesis, and evaluation of inhibitors for severe acute respiratory syndrome 3C-like protease based on phthalhydrazide ketones or heteroaromatic esters.
AID1766398Antileishmanial activity against intracellular Leishmania amazonensis MHOM/BR/77/LTB 0016 amastigotes infected in BALB/c mouse peritoneal macrophage assessed as reduced parasite growth incubated for 72 hrs by PANOTIC staining based assay2021ACS medicinal chemistry letters, Sep-09, Volume: 12, Issue:9
Monocyclic Nitro-heteroaryl Nitrones with Dual Mechanism of Activation: Synthesis and Antileishmanial Activity.
AID1337095Inhibition of human MPO2017ACS medicinal chemistry letters, Feb-09, Volume: 8, Issue:2
From Dynamic Combinatorial Chemistry to
AID1544945Inhibition of NO711 binding to mouse GAT1 expressed in HEK293 cell membranes assessed as residual binding at 1 uM incubated for 4 hrs in presence of NO711 by LC-ESI-MS/MS analysis relative to control2019Bioorganic & medicinal chemistry, 07-01, Volume: 27, Issue:13
Application of the concept of oxime library screening by mass spectrometry (MS) binding assays to pyrrolidine-3-carboxylic acid derivatives as potential inhibitors of γ-aminobutyric acid transporter 1 (GAT1).
AID1766397Antileishmanial activity against Leishmania amazonensis MHOM/BR/77/LTB 0016 promastigotes assessed as inhibition of parasite growth incubated for 72 hrs by resazurin dye based assay2021ACS medicinal chemistry letters, Sep-09, Volume: 12, Issue:9
Monocyclic Nitro-heteroaryl Nitrones with Dual Mechanism of Activation: Synthesis and Antileishmanial Activity.
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.
AID1766396Cytotoxicity against BALB/c mouse peritoneal macrophages assessed as reduction in cell viability incubated for 72 hrs by resazurin dye based fluorescence assay2021ACS medicinal chemistry letters, Sep-09, Volume: 12, Issue:9
Monocyclic Nitro-heteroaryl Nitrones with Dual Mechanism of Activation: Synthesis and Antileishmanial Activity.
AID1766399Antileishmanial activity against Leishmania infantum MHOM/MA/67/ITMAP-263 promastigotes assessed as inhibition of parasite growth incubated for 72 hrs by resazurin dye based assay2021ACS medicinal chemistry letters, Sep-09, Volume: 12, Issue:9
Monocyclic Nitro-heteroaryl Nitrones with Dual Mechanism of Activation: Synthesis and Antileishmanial Activity.
AID1083146Nematotoxic activity against freshly hatched Meloidogyne incognita J2 (root-knot nematode) isolated from tomato roots assessed as induction of microscopic damages in nematode body measured 24 hr after immersion in compound test solutions2012Journal of agricultural and food chemistry, Nov-28, Volume: 60, Issue:47
Nematotoxic phenolic compounds from Melia azedarach against Meloidogyne incognita.
AID1082239Inhibition of Agaricus bisporus (mushroom) tyrosinase2011Journal of agricultural and food chemistry, May-11, Volume: 59, Issue:9
Neonicotinoid insecticides: oxidative stress in planta and metallo-oxidase inhibition.
AID1082888Nematicidal activity against Meloidogyne incognita (root-knot nematode) juveniles J2 assessed as paralysis after 1 day2012Journal of agricultural and food chemistry, Aug-01, Volume: 60, Issue:30
Nematicidal activity of 2-thiophenecarboxaldehyde and methylisothiocyanate from caper (Capparis spinosa) against Meloidogyne incognita.
AID1082237Inhibition of xanthine oxidase2011Journal of agricultural and food chemistry, May-11, Volume: 59, Issue:9
Neonicotinoid insecticides: oxidative stress in planta and metallo-oxidase inhibition.
AID251935Percent inhibition of sickling of sickle red blood (SS) cells under 4% oxygen was evaluated at 5 mM concentration2004Journal of medicinal chemistry, Sep-09, Volume: 47, Issue:19
Structural basis for the potent antisickling effect of a novel class of five-membered heterocyclic aldehydic compounds.
AID1573603Inhibition of NO711 binding to mouse GAT1 expressed in HEK293 cell membranes assessed as residual binding at 1 uM preincubated for 4 hrs followed by NO711 addition and measured after 40 mins by LC-ESI-MS/MS analysis relative to control2018Journal of medicinal chemistry, 11-21, Volume: 61, Issue:22
Novel Allosteric Ligands of γ-Aminobutyric Acid Transporter 1 (GAT1) by MS Based Screening of Pseudostatic Hydrazone Libraries.
AID1081755Nematicidal activity against Meloidogyne incognita J2 (root-knot nematode) assessed as paralysis measured after 1 hr at 28 degC2010Journal of agricultural and food chemistry, Nov-10, Volume: 58, Issue:21
nematicidal carboxylic acids and aldehydes from Melia azedarach fruits.
AID1083149Nematotoxic activity against freshly hatched Meloidogyne incognita J2 (root-knot nematode) isolated from tomato roots assessed as induction of nematode paralysis measured 24 hr after immersion in compound test solutions2012Journal 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 (2,092)

TimeframeStudies, This Drug (%)All Drugs %
pre-1990314 (15.01)18.7374
1990's67 (3.20)18.2507
2000's273 (13.05)29.6817
2010's1063 (50.81)24.3611
2020's375 (17.93)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 72.09

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 Index72.09 (24.57)
Research Supply Index7.68 (2.92)
Research Growth Index5.21 (4.65)
Search Engine Demand Index129.13 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (72.09)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials10 (0.46%)5.53%
Reviews85 (3.94%)6.00%
Case Studies3 (0.14%)4.05%
Observational2 (0.09%)0.25%
Other2,059 (95.37%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]