7-methoxy-6-methyl-1-oxo-3H-2-benzouran-4-carbaldehyde

Details

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Internal ID c6ee4528-761c-4ae7-8a80-abd631e830a6
Taxonomy Organoheterocyclic compounds > Isocoumarans > Isobenzofuranones > Phthalides
IUPAC Name 7-methoxy-6-methyl-1-oxo-3H-2-benzofuran-4-carbaldehyde
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C11H10O4/c1-6-3-7(4-12)8-5-15-11(13)9(8)10(6)14-2/h3-4H,5H2,1-2H3
InChI Key USGIGRXDTKONAL-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C11H10O4
Molecular Weight 206.19 g/mol
Exact Mass 206.05790880 g/mol
Topological Polar Surface Area (TPSA) 52.60 Ų
XlogP 1.10
Atomic LogP (AlogP) 1.49
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 7-methoxy-6-methyl-1-oxo-3H-2-benzouran-4-carbaldehyde

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9940 99.40%
Caco-2 + 0.6271 62.71%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.6590 65.90%
OATP2B1 inhibitior - 0.8621 86.21%
OATP1B1 inhibitior + 0.9129 91.29%
OATP1B3 inhibitior + 0.9791 97.91%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.8173 81.73%
P-glycoprotein inhibitior - 0.9547 95.47%
P-glycoprotein substrate - 0.9458 94.58%
CYP3A4 substrate - 0.5440 54.40%
CYP2C9 substrate - 0.8123 81.23%
CYP2D6 substrate - 0.8484 84.84%
CYP3A4 inhibition - 0.8788 87.88%
CYP2C9 inhibition + 0.8175 81.75%
CYP2C19 inhibition + 0.5153 51.53%
CYP2D6 inhibition - 0.9261 92.61%
CYP1A2 inhibition + 0.8817 88.17%
CYP2C8 inhibition - 0.8713 87.13%
CYP inhibitory promiscuity - 0.5193 51.93%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8683 86.83%
Carcinogenicity (trinary) Non-required 0.6307 63.07%
Eye corrosion - 0.8729 87.29%
Eye irritation + 0.9701 97.01%
Skin irritation - 0.7828 78.28%
Skin corrosion - 0.9611 96.11%
Ames mutagenesis + 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6973 69.73%
Micronuclear + 0.6333 63.33%
Hepatotoxicity + 0.7500 75.00%
skin sensitisation - 0.6637 66.37%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity + 0.5222 52.22%
Mitochondrial toxicity + 0.5875 58.75%
Nephrotoxicity + 0.6113 61.13%
Acute Oral Toxicity (c) III 0.4707 47.07%
Estrogen receptor binding - 0.7027 70.27%
Androgen receptor binding - 0.5837 58.37%
Thyroid receptor binding - 0.8271 82.71%
Glucocorticoid receptor binding - 0.7276 72.76%
Aromatase binding - 0.6306 63.06%
PPAR gamma - 0.7297 72.97%
Honey bee toxicity - 0.9157 91.57%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 0.9411 94.11%

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 97.69% 95.56%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 94.71% 93.40%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.12% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.09% 86.33%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.23% 94.45%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 90.54% 98.11%
CHEMBL4208 P20618 Proteasome component C5 89.84% 90.00%
CHEMBL2581 P07339 Cathepsin D 89.66% 98.95%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 86.82% 94.80%
CHEMBL3401 O75469 Pregnane X receptor 85.55% 94.73%
CHEMBL2535 P11166 Glucose transporter 85.23% 98.75%
CHEMBL4302 P08183 P-glycoprotein 1 84.64% 92.98%

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 131853638
LOTUS LTS0025829
wikiData Q75069946