6-Methoxy-3-methyl-2-benzofuran-4,5-dione

Details

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Internal ID 09f95852-22a5-4cc1-8b10-a3d497518b43
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Aryl ketones
IUPAC Name 6-methoxy-3-methyl-2-benzofuran-4,5-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H8O4/c1-5-8-6(4-14-5)3-7(13-2)9(11)10(8)12/h3-4H,1-2H3
InChI Key SJJQVWSHTVOEAB-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C10H8O4
Molecular Weight 192.17 g/mol
Exact Mass 192.04225873 g/mol
Topological Polar Surface Area (TPSA) 56.50 Ų
XlogP 1.10
Atomic LogP (AlogP) 1.34
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 6-Methoxy-3-methyl-2-benzofuran-4,5-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9958 99.58%
Caco-2 + 0.6748 67.48%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability + 0.7714 77.14%
Subcellular localzation Mitochondria 0.6789 67.89%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9422 94.22%
OATP1B3 inhibitior + 0.9824 98.24%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9385 93.85%
P-glycoprotein inhibitior - 0.8994 89.94%
P-glycoprotein substrate - 0.9652 96.52%
CYP3A4 substrate - 0.5968 59.68%
CYP2C9 substrate - 0.8032 80.32%
CYP2D6 substrate - 0.8590 85.90%
CYP3A4 inhibition - 0.7315 73.15%
CYP2C9 inhibition - 0.8124 81.24%
CYP2C19 inhibition + 0.6827 68.27%
CYP2D6 inhibition - 0.9190 91.90%
CYP1A2 inhibition + 0.9132 91.32%
CYP2C8 inhibition - 0.8748 87.48%
CYP inhibitory promiscuity + 0.7989 79.89%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9043 90.43%
Carcinogenicity (trinary) Non-required 0.4978 49.78%
Eye corrosion - 0.8906 89.06%
Eye irritation + 0.8866 88.66%
Skin irritation - 0.7310 73.10%
Skin corrosion - 0.9660 96.60%
Ames mutagenesis - 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6269 62.69%
Micronuclear + 0.6700 67.00%
Hepatotoxicity + 0.6177 61.77%
skin sensitisation - 0.5654 56.54%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity + 0.6111 61.11%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity + 0.6974 69.74%
Acute Oral Toxicity (c) II 0.3592 35.92%
Estrogen receptor binding - 0.7533 75.33%
Androgen receptor binding - 0.5000 50.00%
Thyroid receptor binding - 0.7210 72.10%
Glucocorticoid receptor binding - 0.8904 89.04%
Aromatase binding - 0.5304 53.04%
PPAR gamma - 0.7829 78.29%
Honey bee toxicity - 0.8004 80.04%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.9418 94.18%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.05% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.01% 91.11%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 86.86% 96.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.54% 86.33%
CHEMBL2581 P07339 Cathepsin D 84.79% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 83.31% 94.73%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.19% 94.00%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 10261969
LOTUS LTS0253330
wikiData Q105254356