Phenol, 4,4'-(1,2-ethenediyl)bis-

Details

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Internal ID d47e0464-3f57-4ce5-8da4-e61a49a9444b
Taxonomy Phenylpropanoids and polyketides > Stilbenes
IUPAC Name 4-[2-(4-hydroxyphenyl)ethenyl]phenol
SMILES (Canonical) C1=CC(=CC=C1C=CC2=CC=C(C=C2)O)O
SMILES (Isomeric) C1=CC(=CC=C1C=CC2=CC=C(C=C2)O)O
InChI InChI=1S/C14H12O2/c15-13-7-3-11(4-8-13)1-2-12-5-9-14(16)10-6-12/h1-10,15-16H
InChI Key XLAIWHIOIFKLEO-UHFFFAOYSA-N
Popularity 32 references in papers

Physical and Chemical Properties

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Molecular Formula C14H12O2
Molecular Weight 212.24 g/mol
Exact Mass 212.083729621 g/mol
Topological Polar Surface Area (TPSA) 40.50 Ų
XlogP 3.50
Atomic LogP (AlogP) 3.27
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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4-[2-(4-hydroxyphenyl)ethenyl]phenol
4,4'-Stilbenediol
Stilbene-4,4'-diol
Oprea1_012705
SCHEMBL145659
DTXSID70859527
XLAIWHIOIFKLEO-UHFFFAOYSA-N
AKOS028108539
FT-0772398
(E/Z)-4-[2-(4-hydroxyphenyl)ethenyl]phenol
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Phenol, 4,4'-(1,2-ethenediyl)bis-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9969 99.69%
Caco-2 + 0.8387 83.87%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.6955 69.55%
OATP2B1 inhibitior - 0.8498 84.98%
OATP1B1 inhibitior + 0.9152 91.52%
OATP1B3 inhibitior + 0.8757 87.57%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.7691 76.91%
P-glycoprotein inhibitior - 0.9671 96.71%
P-glycoprotein substrate - 0.9921 99.21%
CYP3A4 substrate - 0.7980 79.80%
CYP2C9 substrate - 0.5955 59.55%
CYP2D6 substrate - 0.6927 69.27%
CYP3A4 inhibition - 0.6856 68.56%
CYP2C9 inhibition + 0.6038 60.38%
CYP2C19 inhibition + 0.7909 79.09%
CYP2D6 inhibition - 0.9468 94.68%
CYP1A2 inhibition + 0.8031 80.31%
CYP2C8 inhibition - 0.7766 77.66%
CYP inhibitory promiscuity + 0.7844 78.44%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.5412 54.12%
Carcinogenicity (trinary) Non-required 0.4927 49.27%
Eye corrosion - 0.9364 93.64%
Eye irritation + 0.9912 99.12%
Skin irritation + 0.5078 50.78%
Skin corrosion - 0.9512 95.12%
Ames mutagenesis - 0.8300 83.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7670 76.70%
Micronuclear - 0.6000 60.00%
Hepatotoxicity - 0.6153 61.53%
skin sensitisation + 0.9708 97.08%
Respiratory toxicity - 0.9000 90.00%
Reproductive toxicity + 0.7333 73.33%
Mitochondrial toxicity - 0.9250 92.50%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) III 0.7127 71.27%
Estrogen receptor binding + 0.8548 85.48%
Androgen receptor binding + 0.8129 81.29%
Thyroid receptor binding + 0.5414 54.14%
Glucocorticoid receptor binding + 0.6495 64.95%
Aromatase binding + 0.7021 70.21%
PPAR gamma + 0.8560 85.60%
Honey bee toxicity - 0.9475 94.75%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.5400 54.00%
Fish aquatic toxicity + 0.9585 95.85%

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 95.66% 98.35%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.78% 91.11%
CHEMBL3194 P02766 Transthyretin 90.72% 90.71%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.72% 95.56%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.02% 96.00%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 80.31% 91.71%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.06% 86.33%

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.
Paeonia suffruticosa
Yucca periculosa

Cross-Links

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PubChem 92830
LOTUS LTS0016224
wikiData Q27116022