2-Methoxy-2-(4-methoxyphenyl)ethanol

Details

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Internal ID ca2b5b9e-f588-4d4c-9124-66a903d480c6
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzylethers
IUPAC Name 2-methoxy-2-(4-methoxyphenyl)ethanol
SMILES (Canonical) COC1=CC=C(C=C1)C(CO)OC
SMILES (Isomeric) COC1=CC=C(C=C1)C(CO)OC
InChI InChI=1S/C10H14O3/c1-12-9-5-3-8(4-6-9)10(7-11)13-2/h3-6,10-11H,7H2,1-2H3
InChI Key DEFGMDWGWVECKE-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C10H14O3
Molecular Weight 182.22 g/mol
Exact Mass 182.094294304 g/mol
Topological Polar Surface Area (TPSA) 38.70 Ų
XlogP 0.90
Atomic LogP (AlogP) 1.37
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-Methoxy-2-(4-methoxyphenyl)ethanol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9946 99.46%
Caco-2 + 0.8540 85.40%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.8746 87.46%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9394 93.94%
OATP1B3 inhibitior + 0.9406 94.06%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.9339 93.39%
P-glycoprotein inhibitior - 0.9764 97.64%
P-glycoprotein substrate - 0.9308 93.08%
CYP3A4 substrate - 0.7076 70.76%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.3624 36.24%
CYP3A4 inhibition - 0.8693 86.93%
CYP2C9 inhibition - 0.9791 97.91%
CYP2C19 inhibition - 0.8339 83.39%
CYP2D6 inhibition - 0.9539 95.39%
CYP1A2 inhibition - 0.7380 73.80%
CYP2C8 inhibition - 0.9814 98.14%
CYP inhibitory promiscuity - 0.9018 90.18%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.7967 79.67%
Carcinogenicity (trinary) Non-required 0.7091 70.91%
Eye corrosion - 0.8655 86.55%
Eye irritation - 0.5663 56.63%
Skin irritation + 0.5000 50.00%
Skin corrosion - 0.9722 97.22%
Ames mutagenesis - 0.8600 86.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6474 64.74%
Micronuclear - 0.9060 90.60%
Hepatotoxicity - 0.6822 68.22%
skin sensitisation + 0.5068 50.68%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity - 0.7111 71.11%
Mitochondrial toxicity - 0.8625 86.25%
Nephrotoxicity - 0.6879 68.79%
Acute Oral Toxicity (c) III 0.7782 77.82%
Estrogen receptor binding - 0.6549 65.49%
Androgen receptor binding - 0.6327 63.27%
Thyroid receptor binding - 0.7640 76.40%
Glucocorticoid receptor binding - 0.8962 89.62%
Aromatase binding - 0.7733 77.33%
PPAR gamma - 0.7774 77.74%
Honey bee toxicity - 0.9666 96.66%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity - 0.6996 69.96%

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 96.39% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.15% 91.11%
CHEMBL4208 P20618 Proteasome component C5 89.38% 90.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.26% 95.56%
CHEMBL2581 P07339 Cathepsin D 84.49% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.20% 99.17%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.20% 96.00%
CHEMBL1907 P15144 Aminopeptidase N 82.16% 93.31%

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.
Dystaenia takesimana

Cross-Links

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PubChem 88713017
LOTUS LTS0248149
wikiData Q104977138