6-Methoxy-3-methyl-8-(2-phenylethyl)-2,5-dihydro-1-benzoxepine

Details

Top
Internal ID 85c64556-face-498a-a94b-1aba0672bb17
Taxonomy Phenylpropanoids and polyketides > Stilbenes
IUPAC Name 6-methoxy-3-methyl-8-(2-phenylethyl)-2,5-dihydro-1-benzoxepine
SMILES (Canonical) CC1=CCC2=C(C=C(C=C2OC)CCC3=CC=CC=C3)OC1
SMILES (Isomeric) CC1=CCC2=C(C=C(C=C2OC)CCC3=CC=CC=C3)OC1
InChI InChI=1S/C20H22O2/c1-15-8-11-18-19(21-2)12-17(13-20(18)22-14-15)10-9-16-6-4-3-5-7-16/h3-8,12-13H,9-11,14H2,1-2H3
InChI Key UZULBFOIEGXGNE-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C20H22O2
Molecular Weight 294.40 g/mol
Exact Mass 294.161979940 g/mol
Topological Polar Surface Area (TPSA) 18.50 Ų
XlogP 4.70
Atomic LogP (AlogP) 4.36
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 6-Methoxy-3-methyl-8-(2-phenylethyl)-2,5-dihydro-1-benzoxepine

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9975 99.75%
Caco-2 + 0.8604 86.04%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.5806 58.06%
OATP2B1 inhibitior - 0.8628 86.28%
OATP1B1 inhibitior + 0.9492 94.92%
OATP1B3 inhibitior + 0.9566 95.66%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior + 0.8350 83.50%
P-glycoprotein inhibitior + 0.8079 80.79%
P-glycoprotein substrate - 0.6531 65.31%
CYP3A4 substrate + 0.5828 58.28%
CYP2C9 substrate - 0.6025 60.25%
CYP2D6 substrate + 0.5138 51.38%
CYP3A4 inhibition - 0.7254 72.54%
CYP2C9 inhibition - 0.6648 66.48%
CYP2C19 inhibition + 0.7601 76.01%
CYP2D6 inhibition - 0.7276 72.76%
CYP1A2 inhibition + 0.9089 90.89%
CYP2C8 inhibition + 0.6930 69.30%
CYP inhibitory promiscuity + 0.7989 79.89%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8900 89.00%
Carcinogenicity (trinary) Non-required 0.6744 67.44%
Eye corrosion - 0.9799 97.99%
Eye irritation - 0.7500 75.00%
Skin irritation - 0.8038 80.38%
Skin corrosion - 0.9553 95.53%
Ames mutagenesis - 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8799 87.99%
Micronuclear - 0.8200 82.00%
Hepatotoxicity + 0.5302 53.02%
skin sensitisation - 0.6597 65.97%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity + 0.7059 70.59%
Mitochondrial toxicity - 0.5375 53.75%
Nephrotoxicity + 0.6044 60.44%
Acute Oral Toxicity (c) III 0.5508 55.08%
Estrogen receptor binding + 0.7795 77.95%
Androgen receptor binding + 0.7659 76.59%
Thyroid receptor binding + 0.6487 64.87%
Glucocorticoid receptor binding + 0.6587 65.87%
Aromatase binding - 0.5532 55.32%
PPAR gamma + 0.6990 69.90%
Honey bee toxicity - 0.8722 87.22%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.7000 70.00%
Fish aquatic toxicity + 0.9955 99.55%

Targets

Top

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
CHEMBL240 Q12809 HERG 99.64% 89.76%
CHEMBL1293249 Q13887 Kruppel-like factor 5 95.39% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.57% 96.09%
CHEMBL2581 P07339 Cathepsin D 90.13% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.05% 95.56%
CHEMBL5805 Q9NR97 Toll-like receptor 8 87.59% 96.25%
CHEMBL3401 O75469 Pregnane X receptor 86.17% 94.73%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 85.66% 95.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.38% 91.11%
CHEMBL1907 P15144 Aminopeptidase N 84.65% 93.31%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 84.50% 92.62%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.50% 99.17%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 83.93% 85.14%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.45% 94.00%
CHEMBL2535 P11166 Glucose transporter 83.43% 98.75%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 82.91% 95.89%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 81.89% 97.14%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.60% 94.45%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.08% 95.89%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.95% 95.50%
CHEMBL3902 P09211 Glutathione S-transferase Pi 80.87% 93.81%
CHEMBL5939 Q9NZ08 Endoplasmic reticulum aminopeptidase 1 80.66% 100.00%

Plants that contains it

Top
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.
Radula tokiensis

Cross-Links

Top
PubChem 85962939
LOTUS LTS0181633
wikiData Q105282484