3-(1,3-Benzodioxol-5-yl)-1-(4-methoxy-1-benzofuran-5-yl)propan-1-one

Details

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Internal ID de67732e-4f6c-46c9-9d3e-234973158a5c
Taxonomy Benzenoids > Benzene and substituted derivatives > Butyrophenones
IUPAC Name 3-(1,3-benzodioxol-5-yl)-1-(4-methoxy-1-benzofuran-5-yl)propan-1-one
SMILES (Canonical) COC1=C(C=CC2=C1C=CO2)C(=O)CCC3=CC4=C(C=C3)OCO4
SMILES (Isomeric) COC1=C(C=CC2=C1C=CO2)C(=O)CCC3=CC4=C(C=C3)OCO4
InChI InChI=1S/C19H16O5/c1-21-19-13(4-7-16-14(19)8-9-22-16)15(20)5-2-12-3-6-17-18(10-12)24-11-23-17/h3-4,6-10H,2,5,11H2,1H3
InChI Key VZQKDAAIVCVSSU-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C19H16O5
Molecular Weight 324.30 g/mol
Exact Mass 324.09977361 g/mol
Topological Polar Surface Area (TPSA) 57.90 Ų
XlogP 3.70
Atomic LogP (AlogP) 3.99
H-Bond Acceptor 5
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3-(1,3-Benzodioxol-5-yl)-1-(4-methoxy-1-benzofuran-5-yl)propan-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 + 0.9909 99.09%
Caco-2 + 0.8660 86.60%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.8157 81.57%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9291 92.91%
OATP1B3 inhibitior + 0.9704 97.04%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.7145 71.45%
P-glycoprotein inhibitior + 0.8453 84.53%
P-glycoprotein substrate - 0.7822 78.22%
CYP3A4 substrate + 0.5265 52.65%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7529 75.29%
CYP3A4 inhibition + 0.8205 82.05%
CYP2C9 inhibition + 0.8718 87.18%
CYP2C19 inhibition + 0.9479 94.79%
CYP2D6 inhibition + 0.6624 66.24%
CYP1A2 inhibition + 0.7821 78.21%
CYP2C8 inhibition + 0.5221 52.21%
CYP inhibitory promiscuity + 0.8811 88.11%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.3864 38.64%
Eye corrosion - 0.9728 97.28%
Eye irritation - 0.8702 87.02%
Skin irritation - 0.7953 79.53%
Skin corrosion - 0.9618 96.18%
Ames mutagenesis - 0.5164 51.64%
Human Ether-a-go-go-Related Gene inhibition + 0.8121 81.21%
Micronuclear - 0.5149 51.49%
Hepatotoxicity - 0.6091 60.91%
skin sensitisation - 0.6698 66.98%
Respiratory toxicity + 0.6556 65.56%
Reproductive toxicity + 0.7556 75.56%
Mitochondrial toxicity - 0.5375 53.75%
Nephrotoxicity - 0.9124 91.24%
Acute Oral Toxicity (c) III 0.7018 70.18%
Estrogen receptor binding + 0.9665 96.65%
Androgen receptor binding + 0.7362 73.62%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding + 0.8248 82.48%
Aromatase binding + 0.6494 64.94%
PPAR gamma + 0.7370 73.70%
Honey bee toxicity - 0.8173 81.73%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.6955 69.55%
Fish aquatic toxicity + 0.8676 86.76%

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
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 99.08% 96.77%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 98.75% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.80% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.38% 96.09%
CHEMBL2581 P07339 Cathepsin D 95.30% 98.95%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 94.95% 94.80%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.65% 85.14%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.26% 99.17%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 91.55% 92.62%
CHEMBL2535 P11166 Glucose transporter 90.47% 98.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.62% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.75% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.39% 95.56%
CHEMBL4208 P20618 Proteasome component C5 83.95% 90.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.65% 96.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 82.27% 95.50%
CHEMBL3401 O75469 Pregnane X receptor 80.95% 94.73%

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.
Lonchocarpus subglaucescens

Cross-Links

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PubChem 101995341
LOTUS LTS0054601
wikiData Q105299931