3,4-diphenyl-5H-furan-2-one

Details

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Internal ID a1b75ae7-91cd-42e4-8bd1-4bc3432e53b3
Taxonomy Phenylpropanoids and polyketides > Stilbenes
IUPAC Name 3,4-diphenyl-2H-furan-5-one
SMILES (Canonical) C1C(=C(C(=O)O1)C2=CC=CC=C2)C3=CC=CC=C3
SMILES (Isomeric) C1C(=C(C(=O)O1)C2=CC=CC=C2)C3=CC=CC=C3
InChI InChI=1S/C16H12O2/c17-16-15(13-9-5-2-6-10-13)14(11-18-16)12-7-3-1-4-8-12/h1-10H,11H2
InChI Key CPBAHTZRJQATEJ-UHFFFAOYSA-N
Popularity 9 references in papers

Physical and Chemical Properties

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Molecular Formula C16H12O2
Molecular Weight 236.26 g/mol
Exact Mass 236.083729621 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 3.00
Atomic LogP (AlogP) 3.15
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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5635-16-5
3,4-Diphenylfuran-2(5H)-one
3,4-diphenyl-2H-furan-5-one
3,4-diphenyl-2,5-dihydrofuran-2-one
3,4-diphenyl-2(5H)-furanone
CHEMBL1470821
NSC400730
Oprea1_147483
MLS001176843
SCHEMBL5071823
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 3,4-diphenyl-5H-furan-2-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.8624 86.24%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability + 0.7714 77.14%
Subcellular localzation Mitochondria 0.7305 73.05%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9854 98.54%
OATP1B3 inhibitior + 0.9339 93.39%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.7261 72.61%
P-glycoprotein inhibitior - 0.9320 93.20%
P-glycoprotein substrate - 0.9919 99.19%
CYP3A4 substrate - 0.7804 78.04%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8715 87.15%
CYP3A4 inhibition - 0.9638 96.38%
CYP2C9 inhibition - 0.7006 70.06%
CYP2C19 inhibition + 0.5792 57.92%
CYP2D6 inhibition - 0.9015 90.15%
CYP1A2 inhibition + 0.5359 53.59%
CYP2C8 inhibition - 0.9880 98.80%
CYP inhibitory promiscuity + 0.8574 85.74%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8128 81.28%
Carcinogenicity (trinary) Non-required 0.4786 47.86%
Eye corrosion - 0.9286 92.86%
Eye irritation + 0.9080 90.80%
Skin irritation - 0.5914 59.14%
Skin corrosion - 0.9471 94.71%
Ames mutagenesis + 0.6936 69.36%
Human Ether-a-go-go-Related Gene inhibition - 0.6972 69.72%
Micronuclear + 0.5600 56.00%
Hepatotoxicity + 0.8750 87.50%
skin sensitisation - 0.5634 56.34%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity - 0.5444 54.44%
Mitochondrial toxicity - 0.6625 66.25%
Nephrotoxicity + 0.6449 64.49%
Acute Oral Toxicity (c) III 0.5369 53.69%
Estrogen receptor binding + 0.7622 76.22%
Androgen receptor binding + 0.7796 77.96%
Thyroid receptor binding - 0.5758 57.58%
Glucocorticoid receptor binding - 0.5152 51.52%
Aromatase binding + 0.8032 80.32%
PPAR gamma + 0.7652 76.52%
Honey bee toxicity - 0.9089 90.89%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity + 0.7100 71.00%
Fish aquatic toxicity + 0.9941 99.41%

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 96.21% 90.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.47% 95.56%
CHEMBL2581 P07339 Cathepsin D 92.02% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.92% 91.11%
CHEMBL1978 P11511 Cytochrome P450 19A1 88.39% 91.76%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.10% 86.33%
CHEMBL262 P49841 Glycogen synthase kinase-3 beta 80.98% 95.72%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 344049
LOTUS LTS0129619
wikiData Q75067392