2-Propenylfuran

Details

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Internal ID 28826f73-8d9a-4fb6-8428-23e43960499c
Taxonomy Organoheterocyclic compounds > Heteroaromatic compounds
IUPAC Name 2-prop-1-enylfuran
SMILES (Canonical) CC=CC1=CC=CO1
SMILES (Isomeric) CC=CC1=CC=CO1
InChI InChI=1S/C7H8O/c1-2-4-7-5-3-6-8-7/h2-6H,1H3
InChI Key IGWQTPINFQSICW-UHFFFAOYSA-N
Popularity 21 references in papers

Physical and Chemical Properties

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Molecular Formula C7H8O
Molecular Weight 108.14 g/mol
Exact Mass 108.057514874 g/mol
Topological Polar Surface Area (TPSA) 13.10 Ų
XlogP 2.30
Atomic LogP (AlogP) 2.31
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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DTXSID50707638

2D Structure

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2D Structure of 2-Propenylfuran

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9948 99.48%
Caco-2 + 0.9162 91.62%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability + 0.7714 77.14%
Subcellular localzation Plasma membrane 0.3484 34.84%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9300 93.00%
OATP1B3 inhibitior + 0.9710 97.10%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9395 93.95%
P-glycoprotein inhibitior - 0.9857 98.57%
P-glycoprotein substrate - 0.9742 97.42%
CYP3A4 substrate - 0.7402 74.02%
CYP2C9 substrate + 0.6277 62.77%
CYP2D6 substrate - 0.7749 77.49%
CYP3A4 inhibition - 0.9822 98.22%
CYP2C9 inhibition - 0.8572 85.72%
CYP2C19 inhibition - 0.5670 56.70%
CYP2D6 inhibition - 0.9355 93.55%
CYP1A2 inhibition + 0.5409 54.09%
CYP2C8 inhibition - 0.9404 94.04%
CYP inhibitory promiscuity + 0.6157 61.57%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6717 67.17%
Carcinogenicity (trinary) Danger 0.4743 47.43%
Eye corrosion + 0.9626 96.26%
Eye irritation + 0.9964 99.64%
Skin irritation + 0.8565 85.65%
Skin corrosion - 0.5414 54.14%
Ames mutagenesis - 0.8400 84.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7261 72.61%
Micronuclear - 0.5900 59.00%
Hepatotoxicity + 0.5625 56.25%
skin sensitisation + 0.7982 79.82%
Respiratory toxicity - 0.7111 71.11%
Reproductive toxicity + 0.6889 68.89%
Mitochondrial toxicity - 0.6750 67.50%
Nephrotoxicity + 0.5512 55.12%
Acute Oral Toxicity (c) III 0.7432 74.32%
Estrogen receptor binding - 0.9092 90.92%
Androgen receptor binding - 0.9295 92.95%
Thyroid receptor binding - 0.8671 86.71%
Glucocorticoid receptor binding - 0.8561 85.61%
Aromatase binding - 0.8785 87.85%
PPAR gamma - 0.8971 89.71%
Honey bee toxicity - 0.9732 97.32%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.5600 56.00%
Fish aquatic toxicity - 0.5529 55.29%

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 89.82% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.40% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 89.18% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.29% 86.33%
CHEMBL2039 P27338 Monoamine oxidase B 81.99% 92.51%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.44% 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.
Basella alba

Cross-Links

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PubChem 53915682
LOTUS LTS0021419
wikiData Q82641520