(3E)-3-(5-hydroxy-3-oxo-4-phenylfuran-2-ylidene)-1-benzofuran-2-one

Details

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Internal ID 88dba828-a170-45ee-af58-278db34dd12e
Taxonomy Organoheterocyclic compounds > Benzofurans
IUPAC Name (3E)-3-(5-hydroxy-3-oxo-4-phenylfuran-2-ylidene)-1-benzofuran-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C18H10O5/c19-15-13(10-6-2-1-3-7-10)17(20)23-16(15)14-11-8-4-5-9-12(11)22-18(14)21/h1-9,20H/b16-14+
InChI Key QQCXDZWVKTVVSR-JQIJEIRASA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C18H10O5
Molecular Weight 306.30 g/mol
Exact Mass 306.05282342 g/mol
Topological Polar Surface Area (TPSA) 72.80 Ų
XlogP 3.00
Atomic LogP (AlogP) 2.84
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (3E)-3-(5-hydroxy-3-oxo-4-phenylfuran-2-ylidene)-1-benzofuran-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 + 0.9939 99.39%
Caco-2 + 0.6582 65.82%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability + 0.7429 74.29%
Subcellular localzation Mitochondria 0.7587 75.87%
OATP2B1 inhibitior - 0.7216 72.16%
OATP1B1 inhibitior + 0.8894 88.94%
OATP1B3 inhibitior + 0.9067 90.67%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.6094 60.94%
P-glycoprotein inhibitior - 0.5591 55.91%
P-glycoprotein substrate - 0.9709 97.09%
CYP3A4 substrate - 0.5435 54.35%
CYP2C9 substrate - 0.8096 80.96%
CYP2D6 substrate - 0.8820 88.20%
CYP3A4 inhibition - 0.6798 67.98%
CYP2C9 inhibition + 0.8160 81.60%
CYP2C19 inhibition - 0.5481 54.81%
CYP2D6 inhibition - 0.9215 92.15%
CYP1A2 inhibition - 0.5134 51.34%
CYP2C8 inhibition - 0.6510 65.10%
CYP inhibitory promiscuity + 0.6062 60.62%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9443 94.43%
Carcinogenicity (trinary) Danger 0.4443 44.43%
Eye corrosion - 0.9854 98.54%
Eye irritation + 0.9694 96.94%
Skin irritation - 0.5549 55.49%
Skin corrosion - 0.9581 95.81%
Ames mutagenesis - 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7781 77.81%
Micronuclear + 0.8900 89.00%
Hepatotoxicity + 0.6250 62.50%
skin sensitisation - 0.6855 68.55%
Respiratory toxicity + 0.6889 68.89%
Reproductive toxicity + 0.6333 63.33%
Mitochondrial toxicity + 0.6750 67.50%
Nephrotoxicity + 0.7307 73.07%
Acute Oral Toxicity (c) II 0.4200 42.00%
Estrogen receptor binding + 0.6760 67.60%
Androgen receptor binding + 0.7247 72.47%
Thyroid receptor binding + 0.5212 52.12%
Glucocorticoid receptor binding - 0.5506 55.06%
Aromatase binding + 0.5337 53.37%
PPAR gamma + 0.5729 57.29%
Honey bee toxicity - 0.8592 85.92%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity + 0.9964 99.64%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.48% 95.56%
CHEMBL2581 P07339 Cathepsin D 95.54% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 93.12% 99.23%
CHEMBL1951 P21397 Monoamine oxidase A 90.97% 91.49%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.54% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.14% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.79% 89.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 81.05% 95.50%

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 3032551
LOTUS LTS0110700
wikiData Q105225750