4-Methoxy-2(5H)-furanone

Details

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Internal ID 30279f88-da31-408b-aaf5-d89f1a3377b6
Taxonomy Organoheterocyclic compounds > Dihydrofurans > Furanones > Butenolides
IUPAC Name 3-methoxy-2H-furan-5-one
SMILES (Canonical) COC1=CC(=O)OC1
SMILES (Isomeric) COC1=CC(=O)OC1
InChI InChI=1S/C5H6O3/c1-7-4-2-5(6)8-3-4/h2H,3H2,1H3
InChI Key VOYDEHILKLSVNN-UHFFFAOYSA-N
Popularity 13 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 -0.10
Atomic LogP (AlogP) 0.07
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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69556-70-3
4-methoxyfuran-2(5H)-one
3-methoxy-2H-furan-5-one
2(5H)-Furanone,4-methoxy-
methyl tetronate
4-Methoxy-5H-furan-2-one
2(5H)-furanone, 4-methoxy-
MFCD00071565
CHEMBL370888
4-methoxy-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 4-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 + 0.9949 99.49%
Caco-2 + 0.7667 76.67%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Mitochondria 0.7193 71.93%
OATP2B1 inhibitior - 0.8609 86.09%
OATP1B1 inhibitior + 0.9709 97.09%
OATP1B3 inhibitior + 0.9638 96.38%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.8897 88.97%
P-glycoprotein inhibitior - 0.9824 98.24%
P-glycoprotein substrate - 0.9503 95.03%
CYP3A4 substrate - 0.6695 66.95%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8989 89.89%
CYP3A4 inhibition - 0.9876 98.76%
CYP2C9 inhibition - 0.9522 95.22%
CYP2C19 inhibition - 0.8330 83.30%
CYP2D6 inhibition - 0.9552 95.52%
CYP1A2 inhibition + 0.5411 54.11%
CYP2C8 inhibition - 0.9929 99.29%
CYP inhibitory promiscuity - 0.7480 74.80%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8828 88.28%
Carcinogenicity (trinary) Non-required 0.5915 59.15%
Eye corrosion + 0.4654 46.54%
Eye irritation + 0.9869 98.69%
Skin irritation - 0.5522 55.22%
Skin corrosion - 0.8806 88.06%
Ames mutagenesis - 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8365 83.65%
Micronuclear - 0.5900 59.00%
Hepatotoxicity + 0.7658 76.58%
skin sensitisation - 0.7773 77.73%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity - 0.5667 56.67%
Mitochondrial toxicity - 0.7875 78.75%
Nephrotoxicity + 0.6646 66.46%
Acute Oral Toxicity (c) III 0.4570 45.70%
Estrogen receptor binding - 0.9165 91.65%
Androgen receptor binding - 0.6507 65.07%
Thyroid receptor binding - 0.9357 93.57%
Glucocorticoid receptor binding - 0.8967 89.67%
Aromatase binding - 0.8610 86.10%
PPAR gamma - 0.8536 85.36%
Honey bee toxicity - 0.8628 86.28%
Biodegradation + 0.8500 85.00%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity - 0.5901 59.01%

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 90.04% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.46% 91.11%
CHEMBL2581 P07339 Cathepsin D 86.88% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.67% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 82.80% 85.14%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.76% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 80.91% 94.00%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 80.71% 85.30%

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 643477
LOTUS LTS0098623
wikiData Q82124269