3-Methyl-2(5H)-furanone

Details

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Internal ID 165fba3f-b032-4618-a6c4-df3037ed577f
Taxonomy Organoheterocyclic compounds > Dihydrofurans > Furanones > Butenolides
IUPAC Name 4-methyl-2H-furan-5-one
SMILES (Canonical) CC1=CCOC1=O
SMILES (Isomeric) CC1=CCOC1=O
InChI InChI=1S/C5H6O2/c1-4-2-3-7-5(4)6/h2H,3H2,1H3
InChI Key VGHBEMPMIVEGJP-UHFFFAOYSA-N
Popularity 56 references in papers

Physical and Chemical Properties

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Molecular Formula C5H6O2
Molecular Weight 98.10 g/mol
Exact Mass 98.036779430 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 0.60
Atomic LogP (AlogP) 0.49
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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22122-36-7
3-Methylfuran-2(5H)-one
4-methyl-2H-furan-5-one
2(5H)-Furanone, 3-methyl-
2(5H)-Furanone, methyl-
2-Methyl-2-butenolide
UNII-N9KXQ3851K
N9KXQ3851K
.alpha.-Methyl-.gamma.-crotonolactone
3-methyl-2,5-dihydrofuran-2-one
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 3-Methyl-2(5H)-furanone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.7062 70.62%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability + 0.8143 81.43%
Subcellular localzation Mitochondria 0.4787 47.87%
OATP2B1 inhibitior - 0.8671 86.71%
OATP1B1 inhibitior + 0.9689 96.89%
OATP1B3 inhibitior + 0.9553 95.53%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.8847 88.47%
P-glycoprotein inhibitior - 0.9873 98.73%
P-glycoprotein substrate - 0.9904 99.04%
CYP3A4 substrate - 0.7247 72.47%
CYP2C9 substrate - 0.6145 61.45%
CYP2D6 substrate - 0.8990 89.90%
CYP3A4 inhibition - 0.9817 98.17%
CYP2C9 inhibition - 0.9215 92.15%
CYP2C19 inhibition - 0.8464 84.64%
CYP2D6 inhibition - 0.9427 94.27%
CYP1A2 inhibition - 0.5262 52.62%
CYP2C8 inhibition - 0.9949 99.49%
CYP inhibitory promiscuity - 0.7633 76.33%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8144 81.44%
Carcinogenicity (trinary) Non-required 0.5308 53.08%
Eye corrosion + 0.5742 57.42%
Eye irritation + 0.9932 99.32%
Skin irritation + 0.7374 73.74%
Skin corrosion - 0.6960 69.60%
Ames mutagenesis - 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7725 77.25%
Micronuclear - 0.6900 69.00%
Hepatotoxicity + 0.8250 82.50%
skin sensitisation - 0.5776 57.76%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity - 0.6889 68.89%
Mitochondrial toxicity - 0.7250 72.50%
Nephrotoxicity + 0.8163 81.63%
Acute Oral Toxicity (c) III 0.6692 66.92%
Estrogen receptor binding - 0.9644 96.44%
Androgen receptor binding - 0.8978 89.78%
Thyroid receptor binding - 0.9370 93.70%
Glucocorticoid receptor binding - 0.9492 94.92%
Aromatase binding - 0.9012 90.12%
PPAR gamma - 0.9268 92.68%
Honey bee toxicity - 0.9772 97.72%
Biodegradation + 0.8500 85.00%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity + 0.9139 91.39%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.49% 95.56%
CHEMBL2581 P07339 Cathepsin D 88.80% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 88.74% 94.73%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.47% 91.11%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Achillea ageratum
Elsholtzia bodinieri
Morithamnus crassus

Cross-Links

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PubChem 30945
NPASS NPC224693
LOTUS LTS0128074
wikiData Q27284743