2-Acetyl-4-methylfuran

Details

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Internal ID 2dfec960-f6d8-42cc-87a3-16389284ae3f
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Aryl ketones > Aryl alkyl ketones
IUPAC Name 1-(4-methylfuran-2-yl)ethanone
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C7H8O2/c1-5-3-7(6(2)8)9-4-5/h3-4H,1-2H3
InChI Key IYEVQBUAWBANLZ-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C7H8O2
Molecular Weight 124.14 g/mol
Exact Mass 124.052429494 g/mol
Topological Polar Surface Area (TPSA) 30.20 Ų
XlogP 1.40
Atomic LogP (AlogP) 1.79
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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SCHEMBL3385880
IYEVQBUAWBANLZ-UHFFFAOYSA-N

2D Structure

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2D Structure of 2-Acetyl-4-methylfuran

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9943 99.43%
Caco-2 + 0.7508 75.08%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Mitochondria 0.6535 65.35%
OATP2B1 inhibitior - 0.8731 87.31%
OATP1B1 inhibitior + 0.9484 94.84%
OATP1B3 inhibitior + 0.9578 95.78%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9139 91.39%
P-glycoprotein inhibitior - 0.9681 96.81%
P-glycoprotein substrate - 0.9852 98.52%
CYP3A4 substrate - 0.6892 68.92%
CYP2C9 substrate - 0.5878 58.78%
CYP2D6 substrate - 0.8143 81.43%
CYP3A4 inhibition - 0.9603 96.03%
CYP2C9 inhibition - 0.9167 91.67%
CYP2C19 inhibition - 0.7084 70.84%
CYP2D6 inhibition - 0.9307 93.07%
CYP1A2 inhibition + 0.5786 57.86%
CYP2C8 inhibition - 0.9690 96.90%
CYP inhibitory promiscuity - 0.6789 67.89%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7317 73.17%
Carcinogenicity (trinary) Warning 0.4847 48.47%
Eye corrosion + 0.9438 94.38%
Eye irritation + 0.9915 99.15%
Skin irritation + 0.8025 80.25%
Skin corrosion - 0.8636 86.36%
Ames mutagenesis - 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6987 69.87%
Micronuclear + 0.6600 66.00%
Hepatotoxicity + 0.7702 77.02%
skin sensitisation + 0.7987 79.87%
Respiratory toxicity - 0.7778 77.78%
Reproductive toxicity + 0.7556 75.56%
Mitochondrial toxicity - 0.6875 68.75%
Nephrotoxicity - 0.5792 57.92%
Acute Oral Toxicity (c) III 0.7959 79.59%
Estrogen receptor binding - 0.9713 97.13%
Androgen receptor binding - 0.7981 79.81%
Thyroid receptor binding - 0.8984 89.84%
Glucocorticoid receptor binding - 0.9374 93.74%
Aromatase binding - 0.8313 83.13%
PPAR gamma - 0.9264 92.64%
Honey bee toxicity - 0.9511 95.11%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity - 0.6600 66.00%
Fish aquatic toxicity - 0.7712 77.12%

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
CHEMBL3401 O75469 Pregnane X receptor 91.10% 94.73%
CHEMBL2581 P07339 Cathepsin D 88.52% 98.95%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 86.41% 93.65%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.64% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 80.19% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.18% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.12% 89.00%

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.
Gossypium hirsutum

Cross-Links

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PubChem 13237617
LOTUS LTS0191069
wikiData Q104375430