2-Ethylfuran

Details

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Internal ID 953a054f-943f-458c-95ec-8d9567108bb8
Taxonomy Organoheterocyclic compounds > Heteroaromatic compounds
IUPAC Name 2-ethylfuran
SMILES (Canonical) CCC1=CC=CO1
SMILES (Isomeric) CCC1=CC=CO1
InChI InChI=1S/C6H8O/c1-2-6-4-3-5-7-6/h3-5H,2H2,1H3
InChI Key HLPIHRDZBHXTFJ-UHFFFAOYSA-N
Popularity 222 references in papers

Physical and Chemical Properties

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Molecular Formula C6H8O
Molecular Weight 96.13 g/mol
Exact Mass 96.057514874 g/mol
Topological Polar Surface Area (TPSA) 13.10 Ų
XlogP 2.40
Atomic LogP (AlogP) 1.84
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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3208-16-0
Furan, 2-ethyl-
alpha-Ethylfuran
2-Ethyloxole
2-ETHYL FURAN
FEMA No. 3673
CCRIS 4387
2-ethyl-furan
2-Ethyl furane
Furan, .alpha.-ethyl-
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 2-Ethylfuran

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9945 99.45%
Caco-2 + 0.9106 91.06%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability + 0.8000 80.00%
Subcellular localzation Mitochondria 0.4650 46.50%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9111 91.11%
OATP1B3 inhibitior + 0.9616 96.16%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9487 94.87%
P-glycoprotein inhibitior - 0.9892 98.92%
P-glycoprotein substrate - 0.9591 95.91%
CYP3A4 substrate - 0.7751 77.51%
CYP2C9 substrate - 0.8046 80.46%
CYP2D6 substrate - 0.6668 66.68%
CYP3A4 inhibition - 0.9745 97.45%
CYP2C9 inhibition - 0.8109 81.09%
CYP2C19 inhibition + 0.5439 54.39%
CYP2D6 inhibition - 0.9223 92.23%
CYP1A2 inhibition + 0.5566 55.66%
CYP2C8 inhibition - 0.9177 91.77%
CYP inhibitory promiscuity + 0.5126 51.26%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6300 63.00%
Carcinogenicity (trinary) Warning 0.5057 50.57%
Eye corrosion + 0.9165 91.65%
Eye irritation + 0.9819 98.19%
Skin irritation + 0.8152 81.52%
Skin corrosion - 0.8201 82.01%
Ames mutagenesis - 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6603 66.03%
Micronuclear - 0.7500 75.00%
Hepatotoxicity + 0.6250 62.50%
skin sensitisation + 0.7727 77.27%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity + 0.5889 58.89%
Mitochondrial toxicity - 0.8125 81.25%
Nephrotoxicity + 0.4670 46.70%
Acute Oral Toxicity (c) III 0.7432 74.32%
Estrogen receptor binding - 0.9380 93.80%
Androgen receptor binding - 0.9035 90.35%
Thyroid receptor binding - 0.8794 87.94%
Glucocorticoid receptor binding - 0.8214 82.14%
Aromatase binding - 0.7837 78.37%
PPAR gamma - 0.8469 84.69%
Honey bee toxicity - 0.9768 97.68%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity + 0.6000 60.00%
Fish aquatic toxicity - 0.8367 83.67%

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 88.18% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.80% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 87.22% 94.73%
CHEMBL2581 P07339 Cathepsin D 86.56% 98.95%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 84.20% 93.65%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.99% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.31% 95.56%

Plants that contains it

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Cross-Links

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PubChem 18554
NPASS NPC156768
LOTUS LTS0137610
wikiData Q17989420