4-[2-(2-Hydroxyphenyl)ethyl]-2-[4-[2-(3-hydroxyphenyl)ethyl]phenoxy]phenol

Details

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Internal ID 682beb63-03bb-4651-9bf3-ecbb7eb3b784
Taxonomy Lignans, neolignans and related compounds
IUPAC Name 4-[2-(2-hydroxyphenyl)ethyl]-2-[4-[2-(3-hydroxyphenyl)ethyl]phenoxy]phenol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C28H26O4/c29-24-6-3-4-21(18-24)9-8-20-11-15-25(16-12-20)32-28-19-22(13-17-27(28)31)10-14-23-5-1-2-7-26(23)30/h1-7,11-13,15-19,29-31H,8-10,14H2
InChI Key MSUFSHDVARWZEI-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C28H26O4
Molecular Weight 426.50 g/mol
Exact Mass 426.18310931 g/mol
Topological Polar Surface Area (TPSA) 69.90 Ų
XlogP 6.80
Atomic LogP (AlogP) 6.17
H-Bond Acceptor 4
H-Bond Donor 3
Rotatable Bonds 8

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4-[2-(2-Hydroxyphenyl)ethyl]-2-[4-[2-(3-hydroxyphenyl)ethyl]phenoxy]phenol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9302 93.02%
Caco-2 - 0.8529 85.29%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.7286 72.86%
Subcellular localzation Mitochondria 0.9038 90.38%
OATP2B1 inhibitior - 0.5734 57.34%
OATP1B1 inhibitior + 0.9316 93.16%
OATP1B3 inhibitior + 0.8998 89.98%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.8624 86.24%
P-glycoprotein inhibitior + 0.8577 85.77%
P-glycoprotein substrate - 0.6068 60.68%
CYP3A4 substrate + 0.5622 56.22%
CYP2C9 substrate - 0.8019 80.19%
CYP2D6 substrate + 0.4102 41.02%
CYP3A4 inhibition - 0.8582 85.82%
CYP2C9 inhibition + 0.8285 82.85%
CYP2C19 inhibition + 0.8521 85.21%
CYP2D6 inhibition - 0.8942 89.42%
CYP1A2 inhibition + 0.8031 80.31%
CYP2C8 inhibition + 0.8983 89.83%
CYP inhibitory promiscuity + 0.6998 69.98%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.7123 71.23%
Carcinogenicity (trinary) Non-required 0.5472 54.72%
Eye corrosion - 0.9555 95.55%
Eye irritation - 0.6907 69.07%
Skin irritation - 0.6360 63.60%
Skin corrosion - 0.9322 93.22%
Ames mutagenesis - 0.5000 50.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8476 84.76%
Micronuclear - 0.6341 63.41%
Hepatotoxicity - 0.7199 71.99%
skin sensitisation - 0.5686 56.86%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity + 0.5556 55.56%
Mitochondrial toxicity - 0.5875 58.75%
Nephrotoxicity - 0.5566 55.66%
Acute Oral Toxicity (c) III 0.8417 84.17%
Estrogen receptor binding + 0.9174 91.74%
Androgen receptor binding + 0.8369 83.69%
Thyroid receptor binding + 0.6369 63.69%
Glucocorticoid receptor binding + 0.8001 80.01%
Aromatase binding + 0.6312 63.12%
PPAR gamma + 0.8737 87.37%
Honey bee toxicity - 0.6656 66.56%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.5851 58.51%
Fish aquatic toxicity + 0.9566 95.66%

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 98.65% 91.11%
CHEMBL1966 Q02127 Dihydroorotate dehydrogenase 96.33% 96.09%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 95.27% 99.15%
CHEMBL240 Q12809 HERG 93.77% 89.76%
CHEMBL3060 Q9Y345 Glycine transporter 2 93.38% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.21% 86.33%
CHEMBL2581 P07339 Cathepsin D 92.59% 98.95%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 91.87% 83.57%
CHEMBL2535 P11166 Glucose transporter 91.28% 98.75%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.22% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.63% 96.09%
CHEMBL5939 Q9NZ08 Endoplasmic reticulum aminopeptidase 1 88.89% 100.00%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 87.47% 96.95%
CHEMBL226 P30542 Adenosine A1 receptor 87.13% 95.93%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.26% 94.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 85.75% 95.50%
CHEMBL3194 P02766 Transthyretin 85.25% 90.71%
CHEMBL1255126 O15151 Protein Mdm4 84.91% 90.20%
CHEMBL264 Q9Y5N1 Histamine H3 receptor 84.25% 91.43%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 84.08% 95.89%
CHEMBL3902 P09211 Glutathione S-transferase Pi 83.79% 93.81%
CHEMBL3401 O75469 Pregnane X receptor 83.62% 94.73%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 83.59% 92.62%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 83.53% 92.67%
CHEMBL4208 P20618 Proteasome component C5 83.06% 90.00%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 81.22% 94.62%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.09% 95.89%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 81.01% 91.71%
CHEMBL3192 Q9BY41 Histone deacetylase 8 80.67% 93.99%
CHEMBL3761 Q9HCG7 Beta-glucosidase 80.48% 99.00%

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.
Pellia epiphylla

Cross-Links

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PubChem 101712296
LOTUS LTS0031933
wikiData Q105171419