Page last updated: 2024-12-05

2-methylbutanal

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

Description

2-methylbutanal: structure in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

2-methylbutanal : A methylbutanal in which the methyl substituent is at position 2. [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 CID7284
CHEMBL ID2270060
CHEBI ID16182
MeSH IDM0543591

Synonyms (69)

Synonym
CHEBI:16182 ,
ccris 2944
einecs 202-485-6
alpha-methylbutyraldehyde
2-ethylpropanal
alpha-2-methyl-n-butanal
ai3-33276
2-methylbutyraldehyde (natural)
alpha-methylbutanal
methyl ethyl acetaldehyde
alpha-methylbutyric aldehyde
brn 1633540
nsc 77077
fema no. 2691
2-methylbutyric aldehyde
nsc77077
.alpha.-methylbutyric aldehyde
butyraldehyde, 2-methyl-
.alpha.-methylbutanal
2-methyl-1-butanal
methylethylacetaldehyde
wln: vhy2&1
.alpha.-methylbutyraldehyde
2-formylbutane
acetaldehyde, ethylmethyl-
butanal, 2-methyl-
nsc-77077
C02223
96-17-3
2-methylbutanal
2-methylbutyraldehyde
2-methylbutyraldehyde, 95%
2-methylbutyraldehyde, >=95%, fg
M0166
NCGC00249003-01
3-01-00-02813 (beilstein handbook reference)
unii-47h597m1yy
ec 202-485-6
47h597m1yy ,
dtxcid201818
NCGC00256324-01
dtxsid2021818 ,
tox21_302866
cas-96-17-3
NCGC00258794-01
tox21_201242
AKOS009107038
FT-0613025
CHEMBL2270060
(rs)-2-methylbutanal
acetaldehyde, methylethyl-
2-methyl butanal [fcc]
(+/-)-2-methylbutyraldehyde
2-methylbutyraldehyde [fhfi]
2-methyl butanal
2-methylbutan-1-al
2-methyl-butyraldehyde
(.+/-.)-2-methylbutanal
sec-c4h9cho
mfcd00006984
2-methyl butyraldehyde
2-methylbutyraldehyde, analytical standard
2-methylbutyraldehyde, natural, 98%
(+/-)-2-methylbutanal
Q15633241
STR03931
rs)-2-methylbutanal
EN300-26307
F71422
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (3)

RoleDescription
volatile oil componentAny plant metabolite that is found naturally as a component of a volatile oil.
plant metaboliteAny eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
Saccharomyces cerevisiae metaboliteAny fungal metabolite produced during a metabolic reaction in Baker's yeast (Saccharomyces cerevisiae).
[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
methylbutanalAny member of the class of butanals carrying a methyl substituent at an unspecified position.
2-methyl-branched fatty aldehyde
[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 (3)

PathwayProteinsCompounds
Isoleucine Degradation79
L-isoleucine degradation II1212
isoleucine degradation II1312

Protein Targets (6)

Potency Measurements

ProteinTaxonomyMeasurementAverage (µ)Min (ref.)Avg (ref.)Max (ref.)Bioassay(s)
estrogen receptor 2 (ER beta)Homo sapiens (human)Potency4.32330.000657.913322,387.1992AID1259377
retinoic acid nuclear receptor alpha variant 1Homo sapiens (human)Potency48.50840.003041.611522,387.1992AID1159552; AID1159555
estrogen-related nuclear receptor alphaHomo sapiens (human)Potency11.67510.001530.607315,848.9004AID1224841; AID1224842
estrogen nuclear receptor alphaHomo sapiens (human)Potency2.72530.000229.305416,493.5996AID1259383; AID743069
thyroid stimulating hormone receptorHomo sapiens (human)Potency2.89840.001628.015177.1139AID1224843; AID1224895; AID1259385
thyroid hormone receptor beta isoform 2Rattus norvegicus (Norway rat)Potency35.38310.000323.4451159.6830AID743065; AID743067
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Bioassays (9)

Assay IDTitleYearJournalArticle
AID1101114Insecticidal activity against Pseudococcus affinis 2000Journal of agricultural and food chemistry, Sep, Volume: 48, Issue:9
Volatile aldehydes are promising broad-spectrum postharvest insecticides.
AID1101113Insecticidal activity against Bemisia sp.2000Journal of agricultural and food chemistry, Sep, Volume: 48, Issue:9
Volatile aldehydes are promising broad-spectrum postharvest insecticides.
AID1101115Insecticidal activity against Pseudococcus viburni 2000Journal of agricultural and food chemistry, Sep, Volume: 48, Issue:9
Volatile aldehydes are promising broad-spectrum postharvest insecticides.
AID1101148Insecticidal activity against Myzus persicae (green peach aphid) placed under third leaf of naked Iceburg lettuce heads and after compound application for 2 hr through two-tier reduced pressure fumigation at 30 mmHg for 0.5 hr and then 760 mmHg for 1.5 hr2000Journal of agricultural and food chemistry, Sep, Volume: 48, Issue:9
Volatile aldehydes are promising broad-spectrum postharvest insecticides.
AID1101111Insecticidal activity against Brevicoryne brassicae (cabbage aphids)2000Journal of agricultural and food chemistry, Sep, Volume: 48, Issue:9
Volatile aldehydes are promising broad-spectrum postharvest insecticides.
AID1101110Insecticidal activity against Tetranychus urticae (two-spotted spider mite)2000Journal of agricultural and food chemistry, Sep, Volume: 48, Issue:9
Volatile aldehydes are promising broad-spectrum postharvest insecticides.
AID1101147Phytotoxicity in naked Lactuca sativa (lettuce) assessed as residual aldehyde odor after compound application through two-tier reduced pressure fumigation at 30 mmHg for 0.5 hr and then 760 mmHg for 1.5 hr at 23 +/- 1 degC after 2 hr2000Journal of agricultural and food chemistry, Sep, Volume: 48, Issue:9
Volatile aldehydes are promising broad-spectrum postharvest insecticides.
AID1101153Phytotoxicity in naked Lactuca sativa (lettuce) assessed as change in visual quality after compound application through two-tier reduced pressure fumigation at 30 mmHg for 0.5 hr and then 760 mmHg for 1.5 hr at 23 +/- 1 degC after 2 hr2000Journal of agricultural and food chemistry, Sep, Volume: 48, Issue:9
Volatile aldehydes are promising broad-spectrum postharvest insecticides.
AID1101112Insecticidal activity against Frankliniella occidentalis (western flower thrips)2000Journal of agricultural and food chemistry, Sep, Volume: 48, Issue:9
Volatile aldehydes are promising broad-spectrum postharvest insecticides.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (23)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's2 (8.70)29.6817
2010's17 (73.91)24.3611
2020's4 (17.39)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 59.72

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

MetricThis Compound (vs All)
Research Demand Index59.72 (24.57)
Research Supply Index3.22 (2.92)
Research Growth Index5.43 (4.65)
Search Engine Demand Index92.65 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (59.72)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews1 (4.17%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other23 (95.83%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]