2-(1,3-Benzodioxole-5-yl)-3-methyl-5-(2-oxopropyl)benzofuran

Details

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Internal ID 964210b3-3a4f-4d7f-a560-7ee4eec0238f
Taxonomy Phenylpropanoids and polyketides > 2-arylbenzofuran flavonoids
IUPAC Name 1-[2-(1,3-benzodioxol-5-yl)-3-methyl-1-benzofuran-5-yl]propan-2-one
SMILES (Canonical) CC1=C(OC2=C1C=C(C=C2)CC(=O)C)C3=CC4=C(C=C3)OCO4
SMILES (Isomeric) CC1=C(OC2=C1C=C(C=C2)CC(=O)C)C3=CC4=C(C=C3)OCO4
InChI InChI=1S/C19H16O4/c1-11(20)7-13-3-5-16-15(8-13)12(2)19(23-16)14-4-6-17-18(9-14)22-10-21-17/h3-6,8-9H,7,10H2,1-2H3
InChI Key RMYCQPGRJOLBJY-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C19H16O4
Molecular Weight 308.30 g/mol
Exact Mass 308.10485899 g/mol
Topological Polar Surface Area (TPSA) 48.70 Ų
XlogP 3.80
Atomic LogP (AlogP) 4.27
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-(1,3-Benzodioxole-5-yl)-3-methyl-5-(2-oxopropyl)benzofuran

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9925 99.25%
Caco-2 + 0.8173 81.73%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.8207 82.07%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9381 93.81%
OATP1B3 inhibitior + 0.9044 90.44%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.7950 79.50%
P-glycoprotein inhibitior + 0.7807 78.07%
P-glycoprotein substrate - 0.7885 78.85%
CYP3A4 substrate + 0.5256 52.56%
CYP2C9 substrate - 0.7953 79.53%
CYP2D6 substrate - 0.7558 75.58%
CYP3A4 inhibition + 0.8437 84.37%
CYP2C9 inhibition + 0.8375 83.75%
CYP2C19 inhibition + 0.8191 81.91%
CYP2D6 inhibition - 0.6098 60.98%
CYP1A2 inhibition + 0.7998 79.98%
CYP2C8 inhibition + 0.4707 47.07%
CYP inhibitory promiscuity + 0.9087 90.87%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8500 85.00%
Carcinogenicity (trinary) Non-required 0.4554 45.54%
Eye corrosion - 0.9852 98.52%
Eye irritation - 0.9390 93.90%
Skin irritation - 0.7309 73.09%
Skin corrosion - 0.9419 94.19%
Ames mutagenesis + 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8186 81.86%
Micronuclear + 0.5292 52.92%
Hepatotoxicity + 0.7750 77.50%
skin sensitisation + 0.5058 50.58%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity + 0.6556 65.56%
Mitochondrial toxicity - 0.5500 55.00%
Nephrotoxicity - 0.9378 93.78%
Acute Oral Toxicity (c) III 0.6882 68.82%
Estrogen receptor binding + 0.9246 92.46%
Androgen receptor binding + 0.8253 82.53%
Thyroid receptor binding + 0.6466 64.66%
Glucocorticoid receptor binding + 0.9227 92.27%
Aromatase binding + 0.7709 77.09%
PPAR gamma + 0.8692 86.92%
Honey bee toxicity - 0.8656 86.56%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity + 0.9868 98.68%

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
CHEMBL2581 P07339 Cathepsin D 97.94% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.73% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 96.11% 94.45%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 95.44% 96.77%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.66% 89.00%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 92.36% 94.80%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.94% 94.00%
CHEMBL3401 O75469 Pregnane X receptor 88.07% 94.73%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 87.93% 95.50%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 86.56% 96.95%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 86.32% 87.67%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.19% 86.33%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 85.56% 85.14%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 84.87% 92.62%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 84.44% 81.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.12% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.41% 95.56%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 82.74% 93.65%

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.
Piper aequale

Cross-Links

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PubChem 5319626
NPASS NPC36142
LOTUS LTS0095832
wikiData Q105241141