6-hydroxy-4-methoxy-3-(6-methyl-4-oxopyran-3-yl)-3H-2-benzofuran-1-one

Details

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Internal ID 93eb279e-9112-4a03-964f-b281d04b2b48
Taxonomy Organoheterocyclic compounds > Benzofurans > Benzofuranones
IUPAC Name 6-hydroxy-4-methoxy-3-(6-methyl-4-oxopyran-3-yl)-3H-2-benzofuran-1-one
SMILES (Canonical) CC1=CC(=O)C(=CO1)C2C3=C(C=C(C=C3OC)O)C(=O)O2
SMILES (Isomeric) CC1=CC(=O)C(=CO1)C2C3=C(C=C(C=C3OC)O)C(=O)O2
InChI InChI=1S/C15H12O6/c1-7-3-11(17)10(6-20-7)14-13-9(15(18)21-14)4-8(16)5-12(13)19-2/h3-6,14,16H,1-2H3
InChI Key PNHOLPCUUGWDNK-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H12O6
Molecular Weight 288.25 g/mol
Exact Mass 288.06338810 g/mol
Topological Polar Surface Area (TPSA) 82.10 Ų
XlogP 1.20
Atomic LogP (AlogP) 1.92
H-Bond Acceptor 6
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 6-hydroxy-4-methoxy-3-(6-methyl-4-oxopyran-3-yl)-3H-2-benzofuran-1-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9809 98.09%
Caco-2 - 0.6100 61.00%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.8154 81.54%
OATP2B1 inhibitior - 0.8635 86.35%
OATP1B1 inhibitior + 0.8604 86.04%
OATP1B3 inhibitior + 0.9301 93.01%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.8446 84.46%
P-glycoprotein inhibitior - 0.7593 75.93%
P-glycoprotein substrate - 0.7995 79.95%
CYP3A4 substrate + 0.6149 61.49%
CYP2C9 substrate - 0.5848 58.48%
CYP2D6 substrate - 0.8679 86.79%
CYP3A4 inhibition - 0.6286 62.86%
CYP2C9 inhibition + 0.8595 85.95%
CYP2C19 inhibition + 0.5193 51.93%
CYP2D6 inhibition - 0.7607 76.07%
CYP1A2 inhibition + 0.5879 58.79%
CYP2C8 inhibition + 0.5152 51.52%
CYP inhibitory promiscuity + 0.5119 51.19%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Danger 0.4812 48.12%
Eye corrosion - 0.9872 98.72%
Eye irritation - 0.5447 54.47%
Skin irritation - 0.7616 76.16%
Skin corrosion - 0.9684 96.84%
Ames mutagenesis + 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5281 52.81%
Micronuclear + 0.8900 89.00%
Hepatotoxicity + 0.5375 53.75%
skin sensitisation - 0.9261 92.61%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity + 0.7889 78.89%
Mitochondrial toxicity + 0.6500 65.00%
Nephrotoxicity + 0.6303 63.03%
Acute Oral Toxicity (c) II 0.5002 50.02%
Estrogen receptor binding - 0.5404 54.04%
Androgen receptor binding + 0.7177 71.77%
Thyroid receptor binding - 0.5867 58.67%
Glucocorticoid receptor binding + 0.6286 62.86%
Aromatase binding + 0.5323 53.23%
PPAR gamma + 0.6205 62.05%
Honey bee toxicity - 0.8194 81.94%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity + 0.9671 96.71%

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 94.64% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.04% 91.11%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.80% 89.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.56% 94.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.69% 99.23%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.46% 86.33%
CHEMBL2535 P11166 Glucose transporter 87.27% 98.75%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.14% 99.17%
CHEMBL2581 P07339 Cathepsin D 86.62% 98.95%
CHEMBL4208 P20618 Proteasome component C5 85.92% 90.00%
CHEMBL3401 O75469 Pregnane X receptor 84.92% 94.73%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 83.27% 85.14%
CHEMBL3231 Q13464 Rho-associated protein kinase 1 80.13% 95.55%

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 162917002
LOTUS LTS0230435
wikiData Q105211939