4,6-dichloro-7-(2,5-dichloro-3,6-dimethoxy-4-methylphenoxy)-5-methoxy-3H-2-benzofuran-1-one

Details

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Internal ID 7139af98-0859-4407-86fd-21ef887b3571
Taxonomy Organic oxygen compounds > Organooxygen compounds > Ethers > Diarylethers
IUPAC Name 4,6-dichloro-7-(2,5-dichloro-3,6-dimethoxy-4-methylphenoxy)-5-methoxy-3H-2-benzofuran-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C18H14Cl4O6/c1-6-9(19)16(26-4)17(11(21)13(6)24-2)28-14-8-7(5-27-18(8)23)10(20)15(25-3)12(14)22/h5H2,1-4H3
InChI Key HEVPMRDHJYOWRB-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C18H14Cl4O6
Molecular Weight 468.10 g/mol
Exact Mass 467.951499 g/mol
Topological Polar Surface Area (TPSA) 63.20 Ų
XlogP 5.70
Atomic LogP (AlogP) 6.10
H-Bond Acceptor 6
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4,6-dichloro-7-(2,5-dichloro-3,6-dimethoxy-4-methylphenoxy)-5-methoxy-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 + 0.9957 99.57%
Caco-2 + 0.6566 65.66%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.4752 47.52%
OATP2B1 inhibitior - 0.8579 85.79%
OATP1B1 inhibitior + 0.9447 94.47%
OATP1B3 inhibitior + 0.9537 95.37%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.7617 76.17%
P-glycoprotein inhibitior - 0.5266 52.66%
P-glycoprotein substrate - 0.9284 92.84%
CYP3A4 substrate + 0.5777 57.77%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8607 86.07%
CYP3A4 inhibition + 0.5138 51.38%
CYP2C9 inhibition + 0.8676 86.76%
CYP2C19 inhibition + 0.6209 62.09%
CYP2D6 inhibition - 0.8821 88.21%
CYP1A2 inhibition + 0.6627 66.27%
CYP2C8 inhibition - 0.7954 79.54%
CYP inhibitory promiscuity + 0.8817 88.17%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8249 82.49%
Carcinogenicity (trinary) Danger 0.4151 41.51%
Eye corrosion - 0.9708 97.08%
Eye irritation - 0.5918 59.18%
Skin irritation - 0.8320 83.20%
Skin corrosion - 0.9612 96.12%
Ames mutagenesis + 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4673 46.73%
Micronuclear + 0.6640 66.40%
Hepatotoxicity + 0.7875 78.75%
skin sensitisation - 0.7543 75.43%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity + 0.7667 76.67%
Mitochondrial toxicity - 0.5750 57.50%
Nephrotoxicity + 0.7775 77.75%
Acute Oral Toxicity (c) III 0.3860 38.60%
Estrogen receptor binding + 0.8729 87.29%
Androgen receptor binding - 0.6839 68.39%
Thyroid receptor binding + 0.6652 66.52%
Glucocorticoid receptor binding + 0.8490 84.90%
Aromatase binding + 0.6094 60.94%
PPAR gamma + 0.8245 82.45%
Honey bee toxicity - 0.8864 88.64%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.6500 65.00%
Fish aquatic toxicity + 0.9920 99.20%

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 95.24% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.75% 94.45%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.53% 94.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.23% 91.11%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 85.99% 96.77%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.90% 86.33%
CHEMBL1871 P10275 Androgen Receptor 84.75% 96.43%
CHEMBL3401 O75469 Pregnane X receptor 84.46% 94.73%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.12% 96.95%
CHEMBL2581 P07339 Cathepsin D 82.03% 98.95%

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 162892034
LOTUS LTS0032244
wikiData Q105027071