2-Allyl-5-ethoxy-4-methoxyphenol

Details

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Internal ID 9971d91f-ef68-4119-a89e-e673f5e6b3c9
Taxonomy Benzenoids > Phenols > Methoxyphenols
IUPAC Name 5-ethoxy-4-methoxy-2-prop-2-enylphenol
SMILES (Canonical) CCOC1=C(C=C(C(=C1)O)CC=C)OC
SMILES (Isomeric) CCOC1=C(C=C(C(=C1)O)CC=C)OC
InChI InChI=1S/C12H16O3/c1-4-6-9-7-11(14-3)12(15-5-2)8-10(9)13/h4,7-8,13H,1,5-6H2,2-3H3
InChI Key ZGDJSXKWCOVQEY-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C12H16O3
Molecular Weight 208.25 g/mol
Exact Mass 208.109944368 g/mol
Topological Polar Surface Area (TPSA) 38.70 Ų
XlogP 2.90
Atomic LogP (AlogP) 2.53
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

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522598-84-1
DTXSID10344442
ZGDJSXKWCOVQEY-UHFFFAOYSA-N

2D Structure

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2D Structure of 2-Allyl-5-ethoxy-4-methoxyphenol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9953 99.53%
Caco-2 + 0.7105 71.05%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.8652 86.52%
OATP2B1 inhibitior - 0.8601 86.01%
OATP1B1 inhibitior + 0.8761 87.61%
OATP1B3 inhibitior + 0.9775 97.75%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.7344 73.44%
P-glycoprotein inhibitior - 0.9501 95.01%
P-glycoprotein substrate - 0.9092 90.92%
CYP3A4 substrate - 0.5871 58.71%
CYP2C9 substrate + 0.6000 60.00%
CYP2D6 substrate + 0.4334 43.34%
CYP3A4 inhibition - 0.7345 73.45%
CYP2C9 inhibition - 0.8863 88.63%
CYP2C19 inhibition - 0.6253 62.53%
CYP2D6 inhibition - 0.9117 91.17%
CYP1A2 inhibition + 0.6250 62.50%
CYP2C8 inhibition - 0.5915 59.15%
CYP inhibitory promiscuity - 0.5687 56.87%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8483 84.83%
Carcinogenicity (trinary) Non-required 0.6732 67.32%
Eye corrosion - 0.8435 84.35%
Eye irritation + 0.8768 87.68%
Skin irritation - 0.5685 56.85%
Skin corrosion - 0.8808 88.08%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5396 53.96%
Micronuclear - 0.7534 75.34%
Hepatotoxicity + 0.7250 72.50%
skin sensitisation + 0.7174 71.74%
Respiratory toxicity - 0.8333 83.33%
Reproductive toxicity + 0.5889 58.89%
Mitochondrial toxicity - 0.8125 81.25%
Nephrotoxicity + 0.4696 46.96%
Acute Oral Toxicity (c) III 0.8488 84.88%
Estrogen receptor binding + 0.6181 61.81%
Androgen receptor binding - 0.8251 82.51%
Thyroid receptor binding - 0.6300 63.00%
Glucocorticoid receptor binding - 0.7798 77.98%
Aromatase binding - 0.6598 65.98%
PPAR gamma - 0.6166 61.66%
Honey bee toxicity - 0.8469 84.69%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity + 0.9505 95.05%

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 94.23% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.77% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.60% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.49% 86.33%
CHEMBL241 Q14432 Phosphodiesterase 3A 90.09% 92.94%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 85.63% 89.62%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 84.63% 96.95%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.53% 96.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.86% 95.56%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.80% 92.62%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 82.77% 94.00%
CHEMBL3401 O75469 Pregnane X receptor 82.60% 94.73%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 82.49% 97.21%
CHEMBL1937 Q92769 Histone deacetylase 2 82.24% 94.75%
CHEMBL4208 P20618 Proteasome component C5 81.68% 90.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 81.25% 93.99%
CHEMBL2535 P11166 Glucose transporter 80.63% 98.75%

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.
Acorus calamus
Acorus calamus var. angustatus
Acorus gramineus

Cross-Links

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PubChem 596924
NPASS NPC244966