4-(4-Hydroxybenzyl)-5-phenethylbenzene-1,3-diol

Details

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Internal ID 7adb47f4-2d0a-4107-b9f6-4011342cfcca
Taxonomy Phenylpropanoids and polyketides > Stilbenes
IUPAC Name 4-[(4-hydroxyphenyl)methyl]-5-(2-phenylethyl)benzene-1,3-diol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C21H20O3/c22-18-10-7-16(8-11-18)12-20-17(13-19(23)14-21(20)24)9-6-15-4-2-1-3-5-15/h1-5,7-8,10-11,13-14,22-24H,6,9,12H2
InChI Key POCUKQUBQBYJJX-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C21H20O3
Molecular Weight 320.40 g/mol
Exact Mass 320.14124450 g/mol
Topological Polar Surface Area (TPSA) 60.70 Ų
XlogP 5.00
Atomic LogP (AlogP) 4.18
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4-(4-Hydroxybenzyl)-5-phenethylbenzene-1,3-diol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9610 96.10%
Caco-2 - 0.8274 82.74%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.8000 80.00%
Subcellular localzation Mitochondria 0.9143 91.43%
OATP2B1 inhibitior - 0.5686 56.86%
OATP1B1 inhibitior + 0.8115 81.15%
OATP1B3 inhibitior + 0.9188 91.88%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.8902 89.02%
P-glycoprotein inhibitior - 0.7663 76.63%
P-glycoprotein substrate - 0.7938 79.38%
CYP3A4 substrate - 0.5805 58.05%
CYP2C9 substrate - 0.8036 80.36%
CYP2D6 substrate + 0.4561 45.61%
CYP3A4 inhibition - 0.5587 55.87%
CYP2C9 inhibition + 0.8302 83.02%
CYP2C19 inhibition + 0.8472 84.72%
CYP2D6 inhibition - 0.8284 82.84%
CYP1A2 inhibition + 0.5293 52.93%
CYP2C8 inhibition + 0.8937 89.37%
CYP inhibitory promiscuity + 0.7037 70.37%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.7834 78.34%
Carcinogenicity (trinary) Non-required 0.6769 67.69%
Eye corrosion - 0.9537 95.37%
Eye irritation + 0.8033 80.33%
Skin irritation + 0.5056 50.56%
Skin corrosion - 0.7523 75.23%
Ames mutagenesis - 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3754 37.54%
Micronuclear - 0.7400 74.00%
Hepatotoxicity - 0.5875 58.75%
skin sensitisation + 0.5000 50.00%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity - 0.5778 57.78%
Mitochondrial toxicity - 0.5375 53.75%
Nephrotoxicity - 0.6908 69.08%
Acute Oral Toxicity (c) III 0.6768 67.68%
Estrogen receptor binding + 0.9435 94.35%
Androgen receptor binding + 0.8920 89.20%
Thyroid receptor binding + 0.7389 73.89%
Glucocorticoid receptor binding + 0.7021 70.21%
Aromatase binding + 0.7532 75.32%
PPAR gamma + 0.9515 95.15%
Honey bee toxicity - 0.7834 78.34%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.6100 61.00%
Fish aquatic toxicity + 0.9853 98.53%

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 96.70% 91.11%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 96.44% 95.17%
CHEMBL2581 P07339 Cathepsin D 96.29% 98.95%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 94.88% 94.62%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 91.00% 95.50%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 90.39% 91.71%
CHEMBL233 P35372 Mu opioid receptor 89.48% 97.93%
CHEMBL240 Q12809 HERG 89.07% 89.76%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.18% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.67% 95.56%
CHEMBL5805 Q9NR97 Toll-like receptor 8 85.97% 96.25%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.77% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.51% 96.09%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 83.24% 99.15%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 82.19% 83.57%
CHEMBL2535 P11166 Glucose transporter 82.13% 98.75%
CHEMBL5939 Q9NZ08 Endoplasmic reticulum aminopeptidase 1 81.51% 100.00%
CHEMBL3401 O75469 Pregnane X receptor 80.49% 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.
Pleione yunnanensis

Cross-Links

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PubChem 42642928
NPASS NPC111297
LOTUS LTS0265964
wikiData Q105212344