1-(3,4-Dimethoxyfuran-2-yl)ethanone

Details

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Internal ID 156608be-7673-4396-b70e-03559cca3f00
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Aryl ketones > Aryl alkyl ketones
IUPAC Name 1-(3,4-dimethoxyfuran-2-yl)ethanone
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C8H10O4/c1-5(9)7-8(11-3)6(10-2)4-12-7/h4H,1-3H3
InChI Key SZUVOHPGDMWXRD-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C8H10O4
Molecular Weight 170.16 g/mol
Exact Mass 170.05790880 g/mol
Topological Polar Surface Area (TPSA) 48.70 Ų
XlogP 0.90
Atomic LogP (AlogP) 1.50
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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SCHEMBL6857897

2D Structure

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2D Structure of 1-(3,4-Dimethoxyfuran-2-yl)ethanone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9883 98.83%
Caco-2 + 0.6223 62.23%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.7287 72.87%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9574 95.74%
OATP1B3 inhibitior + 0.9787 97.87%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9117 91.17%
P-glycoprotein inhibitior - 0.9508 95.08%
P-glycoprotein substrate - 0.9794 97.94%
CYP3A4 substrate - 0.6200 62.00%
CYP2C9 substrate - 0.6230 62.30%
CYP2D6 substrate - 0.7922 79.22%
CYP3A4 inhibition - 0.8476 84.76%
CYP2C9 inhibition - 0.9548 95.48%
CYP2C19 inhibition + 0.6781 67.81%
CYP2D6 inhibition - 0.9267 92.67%
CYP1A2 inhibition + 0.8917 89.17%
CYP2C8 inhibition - 0.8996 89.96%
CYP inhibitory promiscuity + 0.6310 63.10%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Non-required 0.4741 47.41%
Eye corrosion - 0.6493 64.93%
Eye irritation + 0.9748 97.48%
Skin irritation - 0.7878 78.78%
Skin corrosion - 0.9680 96.80%
Ames mutagenesis - 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5489 54.89%
Micronuclear + 0.5759 57.59%
Hepatotoxicity + 0.6250 62.50%
skin sensitisation - 0.7756 77.56%
Respiratory toxicity - 0.8556 85.56%
Reproductive toxicity + 0.5667 56.67%
Mitochondrial toxicity - 0.7750 77.50%
Nephrotoxicity + 0.4743 47.43%
Acute Oral Toxicity (c) II 0.5258 52.58%
Estrogen receptor binding - 0.8965 89.65%
Androgen receptor binding - 0.7642 76.42%
Thyroid receptor binding - 0.7292 72.92%
Glucocorticoid receptor binding - 0.9104 91.04%
Aromatase binding - 0.8483 84.83%
PPAR gamma - 0.8977 89.77%
Honey bee toxicity - 0.8946 89.46%
Biodegradation + 0.6000 60.00%
Crustacea aquatic toxicity - 0.6855 68.55%
Fish aquatic toxicity + 0.6902 69.02%

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 92.53% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.76% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.38% 94.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.62% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.53% 86.33%

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.
Dictamnus albus

Cross-Links

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PubChem 5316662
NPASS NPC240798
LOTUS LTS0013308
wikiData Q105264424