3-methoxy-2(5H)-furanone

Details

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Internal ID 13e6be14-fcb8-41cc-a7e2-a5386bdd0e3b
Taxonomy Organoheterocyclic compounds > Dihydrofurans > Furanones > Butenolides
IUPAC Name 4-methoxy-2H-furan-5-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C5H6O3/c1-7-4-2-3-8-5(4)6/h2H,3H2,1H3
InChI Key LAPHJRDBCSBIPY-UHFFFAOYSA-N
Popularity 16 references in papers

Physical and Chemical Properties

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Molecular Formula C5H6O3
Molecular Weight 114.10 g/mol
Exact Mass 114.031694049 g/mol
Topological Polar Surface Area (TPSA) 35.50 Ų
XlogP 0.40
Atomic LogP (AlogP) 0.07
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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3-methoxy-2(5h)-furanone
4-methoxy-2H-furan-5-one
3-methoxyfuran-2(5h)-one
2-methoxy-2-buten-4-olide
SCHEMBL5181814
DTXSID60544677

2D Structure

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2D Structure of 3-methoxy-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 + 0.9907 99.07%
Caco-2 + 0.6453 64.53%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability + 0.7429 74.29%
Subcellular localzation Mitochondria 0.7194 71.94%
OATP2B1 inhibitior - 0.8601 86.01%
OATP1B1 inhibitior + 0.9724 97.24%
OATP1B3 inhibitior + 0.9720 97.20%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9261 92.61%
P-glycoprotein inhibitior - 0.9874 98.74%
P-glycoprotein substrate - 0.9850 98.50%
CYP3A4 substrate - 0.7003 70.03%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8806 88.06%
CYP3A4 inhibition - 0.9795 97.95%
CYP2C9 inhibition - 0.9283 92.83%
CYP2C19 inhibition - 0.8099 80.99%
CYP2D6 inhibition - 0.9571 95.71%
CYP1A2 inhibition + 0.5973 59.73%
CYP2C8 inhibition - 0.9835 98.35%
CYP inhibitory promiscuity + 0.5149 51.49%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8528 85.28%
Carcinogenicity (trinary) Non-required 0.5206 52.06%
Eye corrosion - 0.6441 64.41%
Eye irritation + 0.9926 99.26%
Skin irritation - 0.5571 55.71%
Skin corrosion - 0.8784 87.84%
Ames mutagenesis - 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7836 78.36%
Micronuclear + 0.5700 57.00%
Hepatotoxicity + 0.7250 72.50%
skin sensitisation - 0.7415 74.15%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity - 0.6111 61.11%
Mitochondrial toxicity - 0.7875 78.75%
Nephrotoxicity + 0.8181 81.81%
Acute Oral Toxicity (c) III 0.4768 47.68%
Estrogen receptor binding - 0.9731 97.31%
Androgen receptor binding - 0.8806 88.06%
Thyroid receptor binding - 0.9376 93.76%
Glucocorticoid receptor binding - 0.9562 95.62%
Aromatase binding - 0.8713 87.13%
PPAR gamma - 0.9376 93.76%
Honey bee toxicity - 0.9097 90.97%
Biodegradation + 0.8750 87.50%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity - 0.4140 41.40%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.81% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.45% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.41% 86.33%
CHEMBL2581 P07339 Cathepsin D 84.96% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.07% 96.09%
CHEMBL4208 P20618 Proteasome component C5 82.51% 90.00%
CHEMBL2535 P11166 Glucose transporter 81.18% 98.75%

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.
Narthecium ossifragum

Cross-Links

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PubChem 13597600
LOTUS LTS0050692
wikiData Q82421882