Methyl 3-(6,7-dimethoxy-1-benzofuran-5-yl)propanoate

Details

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Internal ID 98d399e5-59b9-4302-a09f-ccac153e8eb7
Taxonomy Organoheterocyclic compounds > Benzofurans
IUPAC Name methyl 3-(6,7-dimethoxy-1-benzofuran-5-yl)propanoate
SMILES (Canonical) COC1=C(C=C2C=COC2=C1OC)CCC(=O)OC
SMILES (Isomeric) COC1=C(C=C2C=COC2=C1OC)CCC(=O)OC
InChI InChI=1S/C14H16O5/c1-16-11(15)5-4-9-8-10-6-7-19-13(10)14(18-3)12(9)17-2/h6-8H,4-5H2,1-3H3
InChI Key BUXWKMDYYFPZLW-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C14H16O5
Molecular Weight 264.27 g/mol
Exact Mass 264.09977361 g/mol
Topological Polar Surface Area (TPSA) 57.90 Ų
XlogP 2.40
Atomic LogP (AlogP) 2.56
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 Methyl 3-(6,7-dimethoxy-1-benzofuran-5-yl)propanoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9894 98.94%
Caco-2 + 0.9034 90.34%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.6478 64.78%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9380 93.80%
OATP1B3 inhibitior + 0.9254 92.54%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.7610 76.10%
P-glycoprotein inhibitior - 0.8719 87.19%
P-glycoprotein substrate - 0.8942 89.42%
CYP3A4 substrate - 0.5980 59.80%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7195 71.95%
CYP3A4 inhibition - 0.8708 87.08%
CYP2C9 inhibition - 0.8527 85.27%
CYP2C19 inhibition + 0.5436 54.36%
CYP2D6 inhibition - 0.9416 94.16%
CYP1A2 inhibition + 0.6915 69.15%
CYP2C8 inhibition - 0.6453 64.53%
CYP inhibitory promiscuity - 0.5680 56.80%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Non-required 0.6000 60.00%
Eye corrosion - 0.9746 97.46%
Eye irritation - 0.5000 50.00%
Skin irritation - 0.7844 78.44%
Skin corrosion - 0.9440 94.40%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3601 36.01%
Micronuclear - 0.7241 72.41%
Hepatotoxicity - 0.5439 54.39%
skin sensitisation - 0.8487 84.87%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity + 0.7889 78.89%
Mitochondrial toxicity + 0.5500 55.00%
Nephrotoxicity - 0.6690 66.90%
Acute Oral Toxicity (c) III 0.4678 46.78%
Estrogen receptor binding + 0.6762 67.62%
Androgen receptor binding + 0.5250 52.50%
Thyroid receptor binding - 0.6242 62.42%
Glucocorticoid receptor binding + 0.6519 65.19%
Aromatase binding - 0.5955 59.55%
PPAR gamma + 0.5820 58.20%
Honey bee toxicity - 0.9598 95.98%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.6700 67.00%
Fish aquatic toxicity + 0.9250 92.50%

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 98.14% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 94.25% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.06% 96.09%
CHEMBL2581 P07339 Cathepsin D 88.95% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.52% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.73% 94.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 85.91% 92.62%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 85.62% 96.00%
CHEMBL3401 O75469 Pregnane X receptor 84.19% 94.73%
CHEMBL4208 P20618 Proteasome component C5 82.28% 90.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 81.70% 85.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.29% 95.56%

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.
Zanthoxylum flavum

Cross-Links

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PubChem 101515651
NPASS NPC143209
LOTUS LTS0186476
wikiData Q104946387