2,4-Dimethoxy-5-(3-phenylprop-2-enyl)phenol

Details

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Internal ID 3a131b45-e6e7-45e8-a0c6-7cb7bb377a31
Taxonomy Phenylpropanoids and polyketides > Linear 1,3-diarylpropanoids > Cinnamylphenols
IUPAC Name 2,4-dimethoxy-5-(3-phenylprop-2-enyl)phenol
SMILES (Canonical) COC1=CC(=C(C=C1CC=CC2=CC=CC=C2)O)OC
SMILES (Isomeric) COC1=CC(=C(C=C1CC=CC2=CC=CC=C2)O)OC
InChI InChI=1S/C17H18O3/c1-19-16-12-17(20-2)15(18)11-14(16)10-6-9-13-7-4-3-5-8-13/h3-9,11-12,18H,10H2,1-2H3
InChI Key BIOKFCCSNSUOLP-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C17H18O3
Molecular Weight 270.32 g/mol
Exact Mass 270.125594432 g/mol
Topological Polar Surface Area (TPSA) 38.70 Ų
XlogP 4.10
Atomic LogP (AlogP) 3.67
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2,4-Dimethoxy-5-(3-phenylprop-2-enyl)phenol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9875 98.75%
Caco-2 + 0.8755 87.55%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.8197 81.97%
OATP2B1 inhibitior - 0.7142 71.42%
OATP1B1 inhibitior - 0.6557 65.57%
OATP1B3 inhibitior + 0.9698 96.98%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.6404 64.04%
P-glycoprotein inhibitior - 0.6643 66.43%
P-glycoprotein substrate - 0.9129 91.29%
CYP3A4 substrate - 0.6214 62.14%
CYP2C9 substrate + 0.5888 58.88%
CYP2D6 substrate + 0.4021 40.21%
CYP3A4 inhibition - 0.7484 74.84%
CYP2C9 inhibition - 0.7349 73.49%
CYP2C19 inhibition + 0.8667 86.67%
CYP2D6 inhibition - 0.7222 72.22%
CYP1A2 inhibition + 0.7462 74.62%
CYP2C8 inhibition + 0.7186 71.86%
CYP inhibitory promiscuity + 0.8893 88.93%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.7621 76.21%
Carcinogenicity (trinary) Non-required 0.5785 57.85%
Eye corrosion - 0.9583 95.83%
Eye irritation + 0.8359 83.59%
Skin irritation - 0.6379 63.79%
Skin corrosion - 0.9045 90.45%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6666 66.66%
Micronuclear - 0.5367 53.67%
Hepatotoxicity - 0.6000 60.00%
skin sensitisation - 0.5830 58.30%
Respiratory toxicity - 0.8111 81.11%
Reproductive toxicity + 0.5778 57.78%
Mitochondrial toxicity - 0.7500 75.00%
Nephrotoxicity - 0.6788 67.88%
Acute Oral Toxicity (c) III 0.7544 75.44%
Estrogen receptor binding + 0.8469 84.69%
Androgen receptor binding - 0.6157 61.57%
Thyroid receptor binding - 0.5088 50.88%
Glucocorticoid receptor binding + 0.5580 55.80%
Aromatase binding - 0.4933 49.33%
PPAR gamma + 0.6297 62.97%
Honey bee toxicity - 0.9099 90.99%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.6700 67.00%
Fish aquatic toxicity + 0.9741 97.41%

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 98.50% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 96.64% 86.33%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 94.39% 96.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.12% 95.56%
CHEMBL3192 Q9BY41 Histone deacetylase 8 93.41% 93.99%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.49% 96.09%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 89.20% 89.62%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.69% 99.17%
CHEMBL2581 P07339 Cathepsin D 88.53% 98.95%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 87.97% 91.71%
CHEMBL3492 P49721 Proteasome Macropain subunit 85.53% 90.24%
CHEMBL4208 P20618 Proteasome component C5 84.74% 90.00%
CHEMBL2535 P11166 Glucose transporter 84.52% 98.75%
CHEMBL3194 P02766 Transthyretin 82.79% 90.71%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 81.96% 95.50%
CHEMBL1255126 O15151 Protein Mdm4 81.13% 90.20%
CHEMBL3401 O75469 Pregnane X receptor 80.73% 94.73%

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.
Dalbergia miscolobium

Cross-Links

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PubChem 320678
LOTUS LTS0066416
wikiData Q104936647