Methyl 7-methoxy-5-benzofurancarboxylate

Details

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Internal ID 20ed446d-de8d-4efb-a778-fe4ae4fc77e7
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzoic acids and derivatives > Methoxybenzoic acids and derivatives > M-methoxybenzoic acids and derivatives
IUPAC Name methyl 7-methoxy-1-benzofuran-5-carboxylate
SMILES (Canonical) COC1=C2C(=CC(=C1)C(=O)OC)C=CO2
SMILES (Isomeric) COC1=C2C(=CC(=C1)C(=O)OC)C=CO2
InChI InChI=1S/C11H10O4/c1-13-9-6-8(11(12)14-2)5-7-3-4-15-10(7)9/h3-6H,1-2H3
InChI Key ISIRVTHXRLKMRV-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C11H10O4
Molecular Weight 206.19 g/mol
Exact Mass 206.05790880 g/mol
Topological Polar Surface Area (TPSA) 48.70 Ų
XlogP 2.10
Atomic LogP (AlogP) 2.23
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Methyl 7-methoxy-5-benzofurancarboxylate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9930 99.30%
Caco-2 + 0.7485 74.85%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Mitochondria 0.5743 57.43%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9258 92.58%
OATP1B3 inhibitior - 0.2301 23.01%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.8582 85.82%
P-glycoprotein inhibitior - 0.9141 91.41%
P-glycoprotein substrate - 0.9400 94.00%
CYP3A4 substrate - 0.6041 60.41%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7934 79.34%
CYP3A4 inhibition - 0.7276 72.76%
CYP2C9 inhibition - 0.8365 83.65%
CYP2C19 inhibition + 0.5067 50.67%
CYP2D6 inhibition - 0.7655 76.55%
CYP1A2 inhibition + 0.9169 91.69%
CYP2C8 inhibition + 0.4814 48.14%
CYP inhibitory promiscuity - 0.5243 52.43%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8886 88.86%
Carcinogenicity (trinary) Warning 0.5137 51.37%
Eye corrosion - 0.8264 82.64%
Eye irritation + 0.8576 85.76%
Skin irritation - 0.6862 68.62%
Skin corrosion - 0.9857 98.57%
Ames mutagenesis - 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6596 65.96%
Micronuclear + 0.7774 77.74%
Hepatotoxicity + 0.5302 53.02%
skin sensitisation - 0.8030 80.30%
Respiratory toxicity - 0.6889 68.89%
Reproductive toxicity + 0.7444 74.44%
Mitochondrial toxicity - 0.5500 55.00%
Nephrotoxicity - 0.6029 60.29%
Acute Oral Toxicity (c) III 0.5522 55.22%
Estrogen receptor binding - 0.5133 51.33%
Androgen receptor binding - 0.6623 66.23%
Thyroid receptor binding - 0.7768 77.68%
Glucocorticoid receptor binding - 0.7678 76.78%
Aromatase binding - 0.5000 50.00%
PPAR gamma - 0.8479 84.79%
Honey bee toxicity - 0.9592 95.92%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity - 0.7366 73.66%
Fish aquatic toxicity + 0.9046 90.46%

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
CHEMBL3060 Q9Y345 Glycine transporter 2 92.97% 99.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.67% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.80% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.17% 86.33%
CHEMBL4208 P20618 Proteasome component C5 88.73% 90.00%
CHEMBL1255126 O15151 Protein Mdm4 83.38% 90.20%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.97% 96.09%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 81.20% 81.11%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.20% 96.00%

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.
Zanthoxylum wutaiense

Cross-Links

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PubChem 91444461
LOTUS LTS0076761
wikiData Q105119564