1-(5-Hydroxy-1-benzofuran-6-yl)-3-phenylprop-2-en-1-one

Details

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Internal ID aef1b738-04ea-4764-aa3a-48dc835115cf
Taxonomy Phenylpropanoids and polyketides > Linear 1,3-diarylpropanoids > Chalcones and dihydrochalcones > Furanochalcones
IUPAC Name 1-(5-hydroxy-1-benzofuran-6-yl)-3-phenylprop-2-en-1-one
SMILES (Canonical) C1=CC=C(C=C1)C=CC(=O)C2=C(C=C3C=COC3=C2)O
SMILES (Isomeric) C1=CC=C(C=C1)C=CC(=O)C2=C(C=C3C=COC3=C2)O
InChI InChI=1S/C17H12O3/c18-15(7-6-12-4-2-1-3-5-12)14-11-17-13(8-9-20-17)10-16(14)19/h1-11,19H
InChI Key ABSGILSFGPQVOT-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C17H12O3
Molecular Weight 264.27 g/mol
Exact Mass 264.078644241 g/mol
Topological Polar Surface Area (TPSA) 50.40 Ų
XlogP 4.30
Atomic LogP (AlogP) 4.03
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1-(5-Hydroxy-1-benzofuran-6-yl)-3-phenylprop-2-en-1-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 + 0.5564 55.64%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.5930 59.30%
OATP2B1 inhibitior - 0.7231 72.31%
OATP1B1 inhibitior + 0.9310 93.10%
OATP1B3 inhibitior + 0.9747 97.47%
MATE1 inhibitior - 0.7200 72.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.6208 62.08%
P-glycoprotein inhibitior - 0.7597 75.97%
P-glycoprotein substrate - 0.9616 96.16%
CYP3A4 substrate - 0.6585 65.85%
CYP2C9 substrate - 0.6154 61.54%
CYP2D6 substrate - 0.8621 86.21%
CYP3A4 inhibition - 0.8283 82.83%
CYP2C9 inhibition + 0.5000 50.00%
CYP2C19 inhibition + 0.8074 80.74%
CYP2D6 inhibition - 0.8965 89.65%
CYP1A2 inhibition + 0.9541 95.41%
CYP2C8 inhibition + 0.6684 66.84%
CYP inhibitory promiscuity + 0.8016 80.16%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Warning 0.3825 38.25%
Eye corrosion - 0.9727 97.27%
Eye irritation + 0.9489 94.89%
Skin irritation + 0.7368 73.68%
Skin corrosion - 0.9872 98.72%
Ames mutagenesis - 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7106 71.06%
Micronuclear + 0.8359 83.59%
Hepatotoxicity - 0.6224 62.24%
skin sensitisation + 0.5459 54.59%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity + 0.5667 56.67%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity - 0.6940 69.40%
Acute Oral Toxicity (c) II 0.3929 39.29%
Estrogen receptor binding + 0.9554 95.54%
Androgen receptor binding + 0.9332 93.32%
Thyroid receptor binding + 0.5988 59.88%
Glucocorticoid receptor binding + 0.7403 74.03%
Aromatase binding + 0.9075 90.75%
PPAR gamma + 0.8468 84.68%
Honey bee toxicity - 0.9107 91.07%
Biodegradation - 0.9750 97.50%
Crustacea aquatic toxicity - 0.6600 66.00%
Fish aquatic toxicity + 0.9847 98.47%

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 98.38% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.77% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.66% 95.56%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 88.96% 95.50%
CHEMBL3192 Q9BY41 Histone deacetylase 8 88.40% 93.99%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.03% 99.23%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.97% 96.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.65% 99.17%
CHEMBL2581 P07339 Cathepsin D 83.89% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 83.48% 94.73%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.00% 89.00%

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.
Millettia erythrocalyx

Cross-Links

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PubChem 162947680
LOTUS LTS0206777
wikiData Q104908803