2-Ethenylfuran

Details

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Internal ID 5196e92f-6cf9-4b5b-ba9e-2046d847a5ae
Taxonomy Organoheterocyclic compounds > Heteroaromatic compounds
IUPAC Name 2-ethenylfuran
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C6H6O/c1-2-6-4-3-5-7-6/h2-5H,1H2
InChI Key QQBUHYQVKJQAOB-UHFFFAOYSA-N
Popularity 181 references in papers

Physical and Chemical Properties

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Molecular Formula C6H6O
Molecular Weight 94.11 g/mol
Exact Mass 94.041864811 g/mol
Topological Polar Surface Area (TPSA) 13.10 Ų
XlogP 2.00
Atomic LogP (AlogP) 1.92
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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Furan, 2-ethenyl-
2-VINYLFURAN
1487-18-9
Vinylfuran
31093-57-9
V5MN67I54D
UNII-V5MN67I54D
2-ethenyl-furan
Furan, ethenyl-
DTXSID8073261
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-Ethenylfuran

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9924 99.24%
Caco-2 + 0.9567 95.67%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability + 0.7571 75.71%
Subcellular localzation Plasma membrane 0.4325 43.25%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9619 96.19%
OATP1B3 inhibitior + 0.9625 96.25%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9490 94.90%
P-glycoprotein inhibitior - 0.9858 98.58%
P-glycoprotein substrate - 0.9945 99.45%
CYP3A4 substrate - 0.7690 76.90%
CYP2C9 substrate - 0.8086 80.86%
CYP2D6 substrate - 0.7523 75.23%
CYP3A4 inhibition - 0.9721 97.21%
CYP2C9 inhibition - 0.8862 88.62%
CYP2C19 inhibition + 0.5276 52.76%
CYP2D6 inhibition - 0.9221 92.21%
CYP1A2 inhibition - 0.5193 51.93%
CYP2C8 inhibition - 0.9169 91.69%
CYP inhibitory promiscuity + 0.5774 57.74%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6617 66.17%
Carcinogenicity (trinary) Warning 0.4232 42.32%
Eye corrosion + 0.9705 97.05%
Eye irritation + 1.0000 100.00%
Skin irritation + 0.8601 86.01%
Skin corrosion + 0.5420 54.20%
Ames mutagenesis - 0.9300 93.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7953 79.53%
Micronuclear - 0.6000 60.00%
Hepatotoxicity + 0.7375 73.75%
skin sensitisation + 0.8194 81.94%
Respiratory toxicity - 0.6889 68.89%
Reproductive toxicity + 0.7111 71.11%
Mitochondrial toxicity - 0.7375 73.75%
Nephrotoxicity + 0.5560 55.60%
Acute Oral Toxicity (c) II 0.5087 50.87%
Estrogen receptor binding - 0.8824 88.24%
Androgen receptor binding - 0.9430 94.30%
Thyroid receptor binding - 0.8620 86.20%
Glucocorticoid receptor binding - 0.8982 89.82%
Aromatase binding - 0.8910 89.10%
PPAR gamma - 0.8455 84.55%
Honey bee toxicity - 0.9261 92.61%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.5900 59.00%
Fish aquatic toxicity + 0.6521 65.21%

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 91.76% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 90.27% 91.49%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.53% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 85.23% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.61% 86.33%

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.
Basella alba

Cross-Links

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PubChem 73881
LOTUS LTS0065560
wikiData Q22028562