3,7,10a-Trimethoxy-1,4,4a,10a-tetrahydrodibenzo-p-dioxin-1-one

Details

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Internal ID 3e2f29e6-d385-4a4b-b70c-7bb5ce38d1a0
Taxonomy Benzenoids > Phenol ethers > Anisoles
IUPAC Name 3,7,10a-trimethoxy-4,4a-dihydrodibenzo-p-dioxin-1-one
SMILES (Canonical) COC1=CC(=O)C2(C(C1)OC3=C(O2)C=CC(=C3)OC)OC
SMILES (Isomeric) COC1=CC(=O)C2(C(C1)OC3=C(O2)C=CC(=C3)OC)OC
InChI InChI=1S/C15H16O6/c1-17-9-4-5-11-12(6-9)20-14-8-10(18-2)7-13(16)15(14,19-3)21-11/h4-7,14H,8H2,1-3H3
InChI Key JHCCCGDYBWNZBF-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H16O6
Molecular Weight 292.28 g/mol
Exact Mass 292.09468823 g/mol
Topological Polar Surface Area (TPSA) 63.20 Ų
XlogP 1.60
Atomic LogP (AlogP) 1.68
H-Bond Acceptor 6
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3,7,10a-Trimethoxy-1,4,4a,10a-tetrahydrodibenzo-p-dioxin-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 + 0.9830 98.30%
Caco-2 + 0.8431 84.31%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.5644 56.44%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9254 92.54%
OATP1B3 inhibitior + 0.9533 95.33%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.5403 54.03%
P-glycoprotein inhibitior - 0.7388 73.88%
P-glycoprotein substrate - 0.8275 82.75%
CYP3A4 substrate + 0.5810 58.10%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8093 80.93%
CYP3A4 inhibition - 0.6313 63.13%
CYP2C9 inhibition - 0.9798 97.98%
CYP2C19 inhibition - 0.5594 55.94%
CYP2D6 inhibition - 0.9085 90.85%
CYP1A2 inhibition + 0.5306 53.06%
CYP2C8 inhibition - 0.7390 73.90%
CYP inhibitory promiscuity + 0.5000 50.00%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9718 97.18%
Carcinogenicity (trinary) Non-required 0.4830 48.30%
Eye corrosion - 0.9801 98.01%
Eye irritation - 0.8855 88.55%
Skin irritation - 0.6907 69.07%
Skin corrosion - 0.9642 96.42%
Ames mutagenesis + 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4829 48.29%
Micronuclear - 0.5000 50.00%
Hepatotoxicity - 0.5687 56.87%
skin sensitisation - 0.7729 77.29%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity - 0.5500 55.00%
Nephrotoxicity + 0.5172 51.72%
Acute Oral Toxicity (c) III 0.3930 39.30%
Estrogen receptor binding + 0.8495 84.95%
Androgen receptor binding + 0.6950 69.50%
Thyroid receptor binding + 0.6407 64.07%
Glucocorticoid receptor binding + 0.7890 78.90%
Aromatase binding + 0.5892 58.92%
PPAR gamma + 0.6578 65.78%
Honey bee toxicity - 0.8442 84.42%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.6500 65.00%
Fish aquatic toxicity + 0.9516 95.16%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.65% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.73% 95.56%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 92.68% 94.80%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.61% 97.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.33% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.16% 96.09%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.92% 94.00%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 88.82% 93.40%
CHEMBL5608 Q16288 NT-3 growth factor receptor 88.26% 95.89%
CHEMBL4208 P20618 Proteasome component C5 88.23% 90.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 87.26% 85.14%
CHEMBL2581 P07339 Cathepsin D 86.59% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.15% 86.33%
CHEMBL3192 Q9BY41 Histone deacetylase 8 84.69% 93.99%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 84.03% 95.71%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 83.55% 97.14%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.81% 92.62%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.09% 96.00%

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.
Hypericum reptans

Cross-Links

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PubChem 155926361
LOTUS LTS0196947
wikiData Q105127869