2-Phenylfuran

Details

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Internal ID 1089164e-d17f-45db-a8b8-3fdd9e779ba5
Taxonomy Benzenoids > Benzene and substituted derivatives
IUPAC Name 2-phenylfuran
SMILES (Canonical) C1=CC=C(C=C1)C2=CC=CO2
SMILES (Isomeric) C1=CC=C(C=C1)C2=CC=CO2
InChI InChI=1S/C10H8O/c1-2-5-9(6-3-1)10-7-4-8-11-10/h1-8H
InChI Key GCXNJAXHHFZVIM-UHFFFAOYSA-N
Popularity 73 references in papers

Physical and Chemical Properties

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Molecular Formula C10H8O
Molecular Weight 144.17 g/mol
Exact Mass 144.057514874 g/mol
Topological Polar Surface Area (TPSA) 13.10 Ų
XlogP 2.60
Atomic LogP (AlogP) 2.95
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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17113-33-6
2-Phenyl-furan
Furan, phenyl-
Furan, 2-phenyl-
Furan,2-phenyl-
SCHEMBL162083
GCXNJAXHHFZVIM-UHFFFAOYSA-
DTXSID00333986
GCXNJAXHHFZVIM-UHFFFAOYSA-N
MFCD00234628
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-Phenylfuran

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9941 99.41%
Caco-2 + 0.9554 95.54%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability + 0.8143 81.43%
Subcellular localzation Mitochondria 0.5613 56.13%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9680 96.80%
OATP1B3 inhibitior + 0.9592 95.92%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.8996 89.96%
P-glycoprotein inhibitior - 0.9760 97.60%
P-glycoprotein substrate - 0.9923 99.23%
CYP3A4 substrate - 0.7694 76.94%
CYP2C9 substrate - 0.8090 80.90%
CYP2D6 substrate - 0.7152 71.52%
CYP3A4 inhibition - 0.9727 97.27%
CYP2C9 inhibition - 0.8631 86.31%
CYP2C19 inhibition + 0.5091 50.91%
CYP2D6 inhibition - 0.9309 93.09%
CYP1A2 inhibition + 0.5945 59.45%
CYP2C8 inhibition - 0.7386 73.86%
CYP inhibitory promiscuity + 0.6909 69.09%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6936 69.36%
Carcinogenicity (trinary) Warning 0.5033 50.33%
Eye corrosion + 0.5697 56.97%
Eye irritation + 1.0000 100.00%
Skin irritation + 0.8131 81.31%
Skin corrosion - 0.9239 92.39%
Ames mutagenesis - 0.8500 85.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7482 74.82%
Micronuclear - 0.6141 61.41%
Hepatotoxicity + 0.8000 80.00%
skin sensitisation + 0.6046 60.46%
Respiratory toxicity - 0.7111 71.11%
Reproductive toxicity + 0.7111 71.11%
Mitochondrial toxicity - 0.7750 77.50%
Nephrotoxicity + 0.5941 59.41%
Acute Oral Toxicity (c) III 0.7604 76.04%
Estrogen receptor binding - 0.5434 54.34%
Androgen receptor binding - 0.6376 63.76%
Thyroid receptor binding - 0.7721 77.21%
Glucocorticoid receptor binding - 0.7817 78.17%
Aromatase binding - 0.5517 55.17%
PPAR gamma - 0.7334 73.34%
Honey bee toxicity - 0.9296 92.96%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.7600 76.00%
Fish aquatic toxicity + 0.6633 66.33%

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
CHEMBL221 P23219 Cyclooxygenase-1 91.30% 90.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.25% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.68% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.92% 86.33%
CHEMBL2954 P25774 Cathepsin S 82.35% 95.60%

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.
Monosis parishii
Persea americana

Cross-Links

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PubChem 519363
LOTUS LTS0054872
wikiData Q82099595