1-Methoxy-2-(phenylmethoxymethyl)benzene

Details

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Internal ID b720de9a-c47b-4e79-9078-20eb0270123e
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzylethers
IUPAC Name 1-methoxy-2-(phenylmethoxymethyl)benzene
SMILES (Canonical) COC1=CC=CC=C1COCC2=CC=CC=C2
SMILES (Isomeric) COC1=CC=CC=C1COCC2=CC=CC=C2
InChI InChI=1S/C15H16O2/c1-16-15-10-6-5-9-14(15)12-17-11-13-7-3-2-4-8-13/h2-10H,11-12H2,1H3
InChI Key QRRJFVCTYOZKEY-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H16O2
Molecular Weight 228.29 g/mol
Exact Mass 228.115029749 g/mol
Topological Polar Surface Area (TPSA) 18.50 Ų
XlogP 3.20
Atomic LogP (AlogP) 3.41
H-Bond Acceptor 2
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 1-Methoxy-2-(phenylmethoxymethyl)benzene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9970 99.70%
Caco-2 + 0.9392 93.92%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.8744 87.44%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9495 94.95%
OATP1B3 inhibitior + 0.9675 96.75%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.5750 57.50%
BSEP inhibitior - 0.6034 60.34%
P-glycoprotein inhibitior - 0.9290 92.90%
P-glycoprotein substrate - 0.7978 79.78%
CYP3A4 substrate - 0.5796 57.96%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.4121 41.21%
CYP3A4 inhibition - 0.9545 95.45%
CYP2C9 inhibition - 0.9324 93.24%
CYP2C19 inhibition + 0.6430 64.30%
CYP2D6 inhibition - 0.8788 87.88%
CYP1A2 inhibition + 0.8922 89.22%
CYP2C8 inhibition - 0.5834 58.34%
CYP inhibitory promiscuity + 0.8019 80.19%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6928 69.28%
Carcinogenicity (trinary) Non-required 0.4722 47.22%
Eye corrosion - 0.9381 93.81%
Eye irritation + 0.8954 89.54%
Skin irritation - 0.8119 81.19%
Skin corrosion - 0.9681 96.81%
Ames mutagenesis - 0.8100 81.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6928 69.28%
Micronuclear - 0.6018 60.18%
Hepatotoxicity + 0.5284 52.84%
skin sensitisation + 0.5519 55.19%
Respiratory toxicity - 0.8000 80.00%
Reproductive toxicity - 0.6556 65.56%
Mitochondrial toxicity - 0.9125 91.25%
Nephrotoxicity + 0.6048 60.48%
Acute Oral Toxicity (c) III 0.7305 73.05%
Estrogen receptor binding + 0.6491 64.91%
Androgen receptor binding - 0.7337 73.37%
Thyroid receptor binding - 0.6268 62.68%
Glucocorticoid receptor binding - 0.8340 83.40%
Aromatase binding + 0.6441 64.41%
PPAR gamma - 0.7435 74.35%
Honey bee toxicity - 0.7517 75.17%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.7100 71.00%
Fish aquatic toxicity + 0.8718 87.18%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.22% 96.09%
CHEMBL2581 P07339 Cathepsin D 92.50% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.93% 86.33%
CHEMBL1255126 O15151 Protein Mdm4 88.62% 90.20%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.35% 95.56%
CHEMBL221 P23219 Cyclooxygenase-1 86.88% 90.17%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.55% 99.17%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 86.15% 95.50%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 84.33% 94.03%
CHEMBL2535 P11166 Glucose transporter 82.79% 98.75%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.36% 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.
Uvaria chamae

Cross-Links

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PubChem 57052255
LOTUS LTS0192413
wikiData Q105226590