Methyl 2-furoate

Details

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Internal ID ca2e0c7e-c195-467c-8e5a-a37f3595cc19
Taxonomy Organoheterocyclic compounds > Furans > Furoic acid and derivatives > Furoic acid esters
IUPAC Name methyl furan-2-carboxylate
SMILES (Canonical) COC(=O)C1=CC=CO1
SMILES (Isomeric) COC(=O)C1=CC=CO1
InChI InChI=1S/C6H6O3/c1-8-6(7)5-3-2-4-9-5/h2-4H,1H3
InChI Key HDJLSECJEQSPKW-UHFFFAOYSA-N
Popularity 172 references in papers

Physical and Chemical Properties

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Molecular Formula C6H6O3
Molecular Weight 126.11 g/mol
Exact Mass 126.031694049 g/mol
Topological Polar Surface Area (TPSA) 39.40 Ų
XlogP 1.00
Atomic LogP (AlogP) 1.07
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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611-13-2
Methyl furan-2-carboxylate
Methyl 2-furancarboxylate
Methyl pyromucate
METHYL FUROATE
2-Furancarboxylic acid, methyl ester
METHYL-2-FUROATE
2-(Methoxycarbonyl)furan
2-FUROIC ACID, METHYL ESTER
Pyromucic acid methyl ester
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Methyl 2-furoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9901 99.01%
Caco-2 + 0.7755 77.55%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Mitochondria 0.7451 74.51%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9431 94.31%
OATP1B3 inhibitior + 0.9652 96.52%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9612 96.12%
P-glycoprotein inhibitior - 0.9865 98.65%
P-glycoprotein substrate - 0.9796 97.96%
CYP3A4 substrate - 0.6238 62.38%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8488 84.88%
CYP3A4 inhibition - 0.9865 98.65%
CYP2C9 inhibition - 0.8861 88.61%
CYP2C19 inhibition - 0.6955 69.55%
CYP2D6 inhibition - 0.9556 95.56%
CYP1A2 inhibition + 0.7309 73.09%
CYP2C8 inhibition - 0.8593 85.93%
CYP inhibitory promiscuity - 0.6592 65.92%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7327 73.27%
Carcinogenicity (trinary) Warning 0.4873 48.73%
Eye corrosion + 0.8907 89.07%
Eye irritation + 0.9961 99.61%
Skin irritation + 0.5226 52.26%
Skin corrosion - 0.8574 85.74%
Ames mutagenesis - 0.8700 87.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6931 69.31%
Micronuclear + 0.5400 54.00%
Hepatotoxicity - 0.5716 57.16%
skin sensitisation + 0.6386 63.86%
Respiratory toxicity - 0.6778 67.78%
Reproductive toxicity + 0.7556 75.56%
Mitochondrial toxicity - 0.8000 80.00%
Nephrotoxicity + 0.5563 55.63%
Acute Oral Toxicity (c) II 0.7705 77.05%
Estrogen receptor binding - 0.9614 96.14%
Androgen receptor binding - 0.9295 92.95%
Thyroid receptor binding - 0.8927 89.27%
Glucocorticoid receptor binding - 0.9354 93.54%
Aromatase binding - 0.8980 89.80%
PPAR gamma - 0.9241 92.41%
Honey bee toxicity - 0.9751 97.51%
Biodegradation + 0.7500 75.00%
Crustacea aquatic toxicity - 0.7300 73.00%
Fish aquatic toxicity - 0.5940 59.40%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.80% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 89.02% 94.73%
CHEMBL2581 P07339 Cathepsin D 88.07% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.61% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.35% 99.17%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 82.60% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.17% 86.33%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.01% 94.45%
CHEMBL4208 P20618 Proteasome component C5 80.56% 90.00%

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.
Actinidia chinensis
Cornus officinalis
Salvia cana

Cross-Links

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PubChem 11902
NPASS NPC48553
LOTUS LTS0002886
wikiData Q105304113