Ethyl 2-furoate

Details

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Internal ID dfe8a87f-239f-48ca-8642-9c8798f03b9a
Taxonomy Organoheterocyclic compounds > Furans > Furoic acid and derivatives > Furoic acid esters
IUPAC Name ethyl furan-2-carboxylate
SMILES (Canonical) CCOC(=O)C1=CC=CO1
SMILES (Isomeric) CCOC(=O)C1=CC=CO1
InChI InChI=1S/C7H8O3/c1-2-9-7(8)6-4-3-5-10-6/h3-5H,2H2,1H3
InChI Key NHXSTXWKZVAVOQ-UHFFFAOYSA-N
Popularity 81 references in papers

Physical and Chemical Properties

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Molecular Formula C7H8O3
Molecular Weight 140.14 g/mol
Exact Mass 140.047344113 g/mol
Topological Polar Surface Area (TPSA) 39.40 Ų
XlogP 1.50
Atomic LogP (AlogP) 1.46
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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Ethyl furan-2-carboxylate
614-99-3
Ethyl furoate
1335-40-6
2-Furancarboxylic acid, ethyl ester
Ethyl 2-furancarboxylate
Ethyl pyromucate
Ethyl2-furoate
Ethyl-2-furoate
2-Carboethoxyfuran
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Ethyl 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 + 0.9952 99.52%
Caco-2 + 0.8415 84.15%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Mitochondria 0.7953 79.53%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9327 93.27%
OATP1B3 inhibitior + 0.9568 95.68%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.8721 87.21%
P-glycoprotein inhibitior - 0.9871 98.71%
P-glycoprotein substrate - 0.9874 98.74%
CYP3A4 substrate - 0.5863 58.63%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8660 86.60%
CYP3A4 inhibition - 0.9752 97.52%
CYP2C9 inhibition - 0.5879 58.79%
CYP2C19 inhibition - 0.5832 58.32%
CYP2D6 inhibition - 0.9442 94.42%
CYP1A2 inhibition + 0.8573 85.73%
CYP2C8 inhibition - 0.8228 82.28%
CYP inhibitory promiscuity + 0.6419 64.19%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7400 74.00%
Carcinogenicity (trinary) Warning 0.4667 46.67%
Eye corrosion + 0.6603 66.03%
Eye irritation + 0.9926 99.26%
Skin irritation + 0.5718 57.18%
Skin corrosion - 0.6881 68.81%
Ames mutagenesis - 0.8400 84.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7608 76.08%
Micronuclear - 0.6967 69.67%
Hepatotoxicity + 0.5750 57.50%
skin sensitisation + 0.7358 73.58%
Respiratory toxicity - 0.7333 73.33%
Reproductive toxicity + 0.6333 63.33%
Mitochondrial toxicity - 0.8500 85.00%
Nephrotoxicity + 0.4542 45.42%
Acute Oral Toxicity (c) III 0.8497 84.97%
Estrogen receptor binding - 0.8660 86.60%
Androgen receptor binding - 0.8944 89.44%
Thyroid receptor binding - 0.9190 91.90%
Glucocorticoid receptor binding - 0.9167 91.67%
Aromatase binding - 0.7812 78.12%
PPAR gamma - 0.9139 91.39%
Honey bee toxicity - 0.9798 97.98%
Biodegradation + 0.7250 72.50%
Crustacea aquatic toxicity - 0.7005 70.05%
Fish aquatic toxicity + 0.6599 65.99%

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 94.39% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 93.32% 94.73%
CHEMBL2581 P07339 Cathepsin D 91.23% 98.95%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 88.40% 93.65%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.56% 99.17%
CHEMBL221 P23219 Cyclooxygenase-1 86.32% 90.17%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.18% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.55% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.93% 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.
Actinidia chinensis

Cross-Links

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PubChem 11980
LOTUS LTS0157652
wikiData Q27288446