Methyl 5-(5-hydroxy-2-methoxyphenyl)furan-3-carboxylate

Details

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Internal ID 41fbd836-43db-4855-b5ff-382a374cc90e
Taxonomy Benzenoids > Phenols > Methoxyphenols
IUPAC Name methyl 5-(5-hydroxy-2-methoxyphenyl)furan-3-carboxylate
SMILES (Canonical) COC1=C(C=C(C=C1)O)C2=CC(=CO2)C(=O)OC
SMILES (Isomeric) COC1=C(C=C(C=C1)O)C2=CC(=CO2)C(=O)OC
InChI InChI=1S/C13H12O5/c1-16-11-4-3-9(14)6-10(11)12-5-8(7-18-12)13(15)17-2/h3-7,14H,1-2H3
InChI Key UPFAUWUMOVGSRQ-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C13H12O5
Molecular Weight 248.23 g/mol
Exact Mass 248.06847348 g/mol
Topological Polar Surface Area (TPSA) 68.90 Ų
XlogP 2.10
Atomic LogP (AlogP) 2.45
H-Bond Acceptor 5
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 Methyl 5-(5-hydroxy-2-methoxyphenyl)furan-3-carboxylate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9854 98.54%
Caco-2 + 0.7602 76.02%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.8668 86.68%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8287 82.87%
OATP1B3 inhibitior + 0.9419 94.19%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.7830 78.30%
P-glycoprotein inhibitior - 0.7371 73.71%
P-glycoprotein substrate - 0.7987 79.87%
CYP3A4 substrate + 0.5237 52.37%
CYP2C9 substrate - 0.8141 81.41%
CYP2D6 substrate - 0.8290 82.90%
CYP3A4 inhibition - 0.8413 84.13%
CYP2C9 inhibition - 0.6575 65.75%
CYP2C19 inhibition + 0.6916 69.16%
CYP2D6 inhibition - 0.9321 93.21%
CYP1A2 inhibition + 0.5554 55.54%
CYP2C8 inhibition + 0.8117 81.17%
CYP inhibitory promiscuity + 0.6354 63.54%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8051 80.51%
Carcinogenicity (trinary) Non-required 0.5290 52.90%
Eye corrosion - 0.9467 94.67%
Eye irritation + 0.8502 85.02%
Skin irritation - 0.7241 72.41%
Skin corrosion - 0.9814 98.14%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5000 50.00%
Micronuclear + 0.7359 73.59%
Hepatotoxicity + 0.5677 56.77%
skin sensitisation - 0.9336 93.36%
Respiratory toxicity - 0.7889 78.89%
Reproductive toxicity + 0.5778 57.78%
Mitochondrial toxicity - 0.6125 61.25%
Nephrotoxicity + 0.4799 47.99%
Acute Oral Toxicity (c) II 0.5418 54.18%
Estrogen receptor binding + 0.8517 85.17%
Androgen receptor binding + 0.7419 74.19%
Thyroid receptor binding + 0.5436 54.36%
Glucocorticoid receptor binding + 0.5572 55.72%
Aromatase binding + 0.7246 72.46%
PPAR gamma + 0.5552 55.52%
Honey bee toxicity - 0.9181 91.81%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.7200 72.00%
Fish aquatic toxicity + 0.9570 95.70%

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 94.21% 99.17%
CHEMBL1255126 O15151 Protein Mdm4 93.85% 90.20%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.34% 86.33%
CHEMBL2535 P11166 Glucose transporter 91.73% 98.75%
CHEMBL4208 P20618 Proteasome component C5 91.30% 90.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.05% 94.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.94% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.70% 91.11%
CHEMBL3194 P02766 Transthyretin 83.06% 90.71%
CHEMBL2581 P07339 Cathepsin D 82.59% 98.95%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 81.52% 94.42%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 80.72% 91.07%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 80.10% 90.71%

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.
Heliotropium sarmentosum

Cross-Links

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PubChem 5324825
LOTUS LTS0174121
wikiData Q105276759