2-Butyl-4-ethenylfuran

Details

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Internal ID a2da81ff-9691-494c-aa7e-cb43a01ba3a7
Taxonomy Organoheterocyclic compounds > Heteroaromatic compounds
IUPAC Name 2-butyl-4-ethenylfuran
SMILES (Canonical) CCCCC1=CC(=CO1)C=C
SMILES (Isomeric) CCCCC1=CC(=CO1)C=C
InChI InChI=1S/C10H14O/c1-3-5-6-10-7-9(4-2)8-11-10/h4,7-8H,2-3,5-6H2,1H3
InChI Key GOTQEXMDSCBZIH-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C10H14O
Molecular Weight 150.22 g/mol
Exact Mass 150.104465066 g/mol
Topological Polar Surface Area (TPSA) 13.10 Ų
XlogP 3.50
Atomic LogP (AlogP) 3.27
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-Butyl-4-ethenylfuran

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9951 99.51%
Caco-2 + 0.9463 94.63%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Plasma membrane 0.6482 64.82%
OATP2B1 inhibitior - 0.8576 85.76%
OATP1B1 inhibitior + 0.8822 88.22%
OATP1B3 inhibitior + 0.9463 94.63%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.8897 88.97%
P-glycoprotein inhibitior - 0.9846 98.46%
P-glycoprotein substrate - 0.8726 87.26%
CYP3A4 substrate - 0.6327 63.27%
CYP2C9 substrate - 0.8037 80.37%
CYP2D6 substrate - 0.7214 72.14%
CYP3A4 inhibition - 0.9295 92.95%
CYP2C9 inhibition - 0.8272 82.72%
CYP2C19 inhibition + 0.5831 58.31%
CYP2D6 inhibition - 0.9119 91.19%
CYP1A2 inhibition + 0.6708 67.08%
CYP2C8 inhibition - 0.6953 69.53%
CYP inhibitory promiscuity + 0.5568 55.68%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8300 83.00%
Carcinogenicity (trinary) Warning 0.3778 37.78%
Eye corrosion + 0.6860 68.60%
Eye irritation + 0.9204 92.04%
Skin irritation + 0.7594 75.94%
Skin corrosion - 0.8912 89.12%
Ames mutagenesis - 0.8400 84.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5825 58.25%
Micronuclear - 0.8700 87.00%
Hepatotoxicity + 0.5250 52.50%
skin sensitisation + 0.7893 78.93%
Respiratory toxicity - 0.6889 68.89%
Reproductive toxicity + 0.5222 52.22%
Mitochondrial toxicity - 0.8750 87.50%
Nephrotoxicity - 0.6442 64.42%
Acute Oral Toxicity (c) III 0.7872 78.72%
Estrogen receptor binding - 0.8848 88.48%
Androgen receptor binding - 0.6540 65.40%
Thyroid receptor binding - 0.7722 77.22%
Glucocorticoid receptor binding - 0.7941 79.41%
Aromatase binding - 0.7108 71.08%
PPAR gamma - 0.7265 72.65%
Honey bee toxicity - 0.9608 96.08%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.8089 80.89%

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
CHEMBL2581 P07339 Cathepsin D 93.58% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.38% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.99% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 91.66% 94.73%
CHEMBL240 Q12809 HERG 90.52% 89.76%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 87.82% 92.08%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.33% 94.45%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.48% 99.17%
CHEMBL2885 P07451 Carbonic anhydrase III 82.04% 87.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 80.73% 96.09%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.39% 96.00%

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.
Gossypium hirsutum

Cross-Links

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PubChem 163195750
LOTUS LTS0198551
wikiData Q105014569