Furfuryl methyl ether

Details

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Internal ID aa2a06dc-64ba-470c-8f7d-8b05801478c9
Taxonomy Organoheterocyclic compounds > Heteroaromatic compounds
IUPAC Name 2-(methoxymethyl)furan
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C6H8O2/c1-7-5-6-3-2-4-8-6/h2-4H,5H2,1H3
InChI Key GANSPRKOWQQXPE-UHFFFAOYSA-N
Popularity 30 references in papers

Physical and Chemical Properties

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Molecular Formula C6H8O2
Molecular Weight 112.13 g/mol
Exact Mass 112.052429494 g/mol
Topological Polar Surface Area (TPSA) 22.40 Ų
XlogP 0.90
Atomic LogP (AlogP) 1.43
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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Furfuryl methyl ether
13679-46-4
Furan, 2-(methoxymethyl)-
2-Furfuryl methyl ether
Methyl furfuryl ether
furfurylmethylether
Furan, (methoxymethyl)-
FEMA No. 3159
RRM754RXFN
NSC-35554
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Furfuryl methyl ether

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9911 99.11%
Caco-2 + 0.8483 84.83%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.6069 60.69%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9279 92.79%
OATP1B3 inhibitior + 0.9526 95.26%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9562 95.62%
P-glycoprotein inhibitior - 0.9886 98.86%
P-glycoprotein substrate - 0.9729 97.29%
CYP3A4 substrate - 0.6677 66.77%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7274 72.74%
CYP3A4 inhibition - 0.9837 98.37%
CYP2C9 inhibition - 0.8285 82.85%
CYP2C19 inhibition - 0.5525 55.25%
CYP2D6 inhibition - 0.9019 90.19%
CYP1A2 inhibition + 0.5430 54.30%
CYP2C8 inhibition - 0.8069 80.69%
CYP inhibitory promiscuity - 0.6847 68.47%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7317 73.17%
Carcinogenicity (trinary) Warning 0.4069 40.69%
Eye corrosion + 0.5111 51.11%
Eye irritation + 0.9840 98.40%
Skin irritation + 0.5326 53.26%
Skin corrosion - 0.9204 92.04%
Ames mutagenesis - 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6235 62.35%
Micronuclear - 0.8067 80.67%
Hepatotoxicity - 0.5341 53.41%
skin sensitisation + 0.8980 89.80%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity + 0.6333 63.33%
Mitochondrial toxicity - 0.8000 80.00%
Nephrotoxicity + 0.6696 66.96%
Acute Oral Toxicity (c) III 0.4649 46.49%
Estrogen receptor binding - 0.9437 94.37%
Androgen receptor binding - 0.8683 86.83%
Thyroid receptor binding - 0.9011 90.11%
Glucocorticoid receptor binding - 0.8815 88.15%
Aromatase binding - 0.8926 89.26%
PPAR gamma - 0.8368 83.68%
Honey bee toxicity - 0.9522 95.22%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity + 0.6600 66.00%
Fish aquatic toxicity - 0.9099 90.99%

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 92.92% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.86% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 85.71% 94.73%
CHEMBL2581 P07339 Cathepsin D 84.47% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.28% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 82.83% 94.00%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 61661
LOTUS LTS0146020
wikiData Q27288260