4-(3,4,5-Trimethoxyphenyl)phenol

Details

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Internal ID dc64f4fd-5698-45e5-b7ba-4b639a2df3c7
Taxonomy Benzenoids > Benzene and substituted derivatives > Biphenyls and derivatives
IUPAC Name 4-(3,4,5-trimethoxyphenyl)phenol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H16O4/c1-17-13-8-11(9-14(18-2)15(13)19-3)10-4-6-12(16)7-5-10/h4-9,16H,1-3H3
InChI Key BQOPGIGJYFACOV-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H16O4
Molecular Weight 260.28 g/mol
Exact Mass 260.10485899 g/mol
Topological Polar Surface Area (TPSA) 47.90 Ų
XlogP 3.10
Atomic LogP (AlogP) 3.09
H-Bond Acceptor 4
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 4-(3,4,5-Trimethoxyphenyl)phenol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9895 98.95%
Caco-2 + 0.9452 94.52%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.8847 88.47%
OATP2B1 inhibitior - 0.8602 86.02%
OATP1B1 inhibitior + 0.9369 93.69%
OATP1B3 inhibitior + 0.9386 93.86%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.6020 60.20%
P-glycoprotein inhibitior - 0.8814 88.14%
P-glycoprotein substrate - 0.9497 94.97%
CYP3A4 substrate - 0.5994 59.94%
CYP2C9 substrate - 0.7845 78.45%
CYP2D6 substrate + 0.4222 42.22%
CYP3A4 inhibition - 0.7715 77.15%
CYP2C9 inhibition - 0.9415 94.15%
CYP2C19 inhibition + 0.5994 59.94%
CYP2D6 inhibition - 0.9337 93.37%
CYP1A2 inhibition + 0.5492 54.92%
CYP2C8 inhibition + 0.9042 90.42%
CYP inhibitory promiscuity + 0.6534 65.34%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.7450 74.50%
Carcinogenicity (trinary) Non-required 0.5469 54.69%
Eye corrosion - 0.9752 97.52%
Eye irritation + 0.9186 91.86%
Skin irritation - 0.7860 78.60%
Skin corrosion - 0.9712 97.12%
Ames mutagenesis - 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3675 36.75%
Micronuclear - 0.5167 51.67%
Hepatotoxicity - 0.6519 65.19%
skin sensitisation - 0.9092 90.92%
Respiratory toxicity - 0.8556 85.56%
Reproductive toxicity + 0.6000 60.00%
Mitochondrial toxicity - 0.8500 85.00%
Nephrotoxicity - 0.5785 57.85%
Acute Oral Toxicity (c) III 0.6352 63.52%
Estrogen receptor binding + 0.6878 68.78%
Androgen receptor binding + 0.8519 85.19%
Thyroid receptor binding + 0.7259 72.59%
Glucocorticoid receptor binding + 0.5819 58.19%
Aromatase binding + 0.6459 64.59%
PPAR gamma - 0.6273 62.73%
Honey bee toxicity - 0.9063 90.63%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.6951 69.51%
Fish aquatic toxicity + 0.9600 96.00%

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
CHEMBL242 Q92731 Estrogen receptor beta 94.08% 98.35%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.20% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.30% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.77% 94.00%
CHEMBL3438 Q05513 Protein kinase C zeta 87.67% 88.48%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.07% 99.17%
CHEMBL4355 O14976 Serine/threonine-protein kinase GAK 86.74% 89.32%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.45% 91.11%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 83.34% 99.15%
CHEMBL2581 P07339 Cathepsin D 82.85% 98.95%
CHEMBL1907 P15144 Aminopeptidase N 82.03% 93.31%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.54% 95.56%

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.
Hypericum reflexum

Cross-Links

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PubChem 14757910
LOTUS LTS0253632
wikiData Q104944486