Phenol, (Z)-

Details

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Internal ID 7247a52d-ca92-4e15-9c75-e124deb3a8b6
Taxonomy Phenylpropanoids and polyketides > Stilbenes
IUPAC Name 4-[(Z)-2-(3-methoxyphenyl)ethenyl]phenol
SMILES (Canonical) COC1=CC=CC(=C1)C=CC2=CC=C(C=C2)O
SMILES (Isomeric) COC1=CC=CC(=C1)/C=C\C2=CC=C(C=C2)O
InChI InChI=1S/C15H14O2/c1-17-15-4-2-3-13(11-15)6-5-12-7-9-14(16)10-8-12/h2-11,16H,1H3/b6-5-
InChI Key ZVJLZUWCAUTTBS-WAYWQWQTSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C15H14O2
Molecular Weight 226.27 g/mol
Exact Mass 226.099379685 g/mol
Topological Polar Surface Area (TPSA) 29.50 Ų
XlogP 4.00
Atomic LogP (AlogP) 3.57
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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Phenol, (Z)-
(Z)-3'-Methoxystilben-4-ol
CHEMBL476677
NSC-684913

2D Structure

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2D Structure of Phenol, (Z)-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.7523 75.23%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.7791 77.91%
OATP2B1 inhibitior - 0.8602 86.02%
OATP1B1 inhibitior + 0.8869 88.69%
OATP1B3 inhibitior + 0.9711 97.11%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.6127 61.27%
P-glycoprotein inhibitior - 0.9115 91.15%
P-glycoprotein substrate - 0.9373 93.73%
CYP3A4 substrate - 0.5820 58.20%
CYP2C9 substrate - 0.5963 59.63%
CYP2D6 substrate - 0.6581 65.81%
CYP3A4 inhibition - 0.8046 80.46%
CYP2C9 inhibition - 0.7619 76.19%
CYP2C19 inhibition + 0.8173 81.73%
CYP2D6 inhibition - 0.9341 93.41%
CYP1A2 inhibition + 0.8988 89.88%
CYP2C8 inhibition + 0.6791 67.91%
CYP inhibitory promiscuity + 0.6186 61.86%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.5767 57.67%
Carcinogenicity (trinary) Non-required 0.4638 46.38%
Eye corrosion - 0.9757 97.57%
Eye irritation + 0.9804 98.04%
Skin irritation - 0.7079 70.79%
Skin corrosion - 0.9650 96.50%
Ames mutagenesis - 0.6900 69.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6841 68.41%
Micronuclear - 0.6800 68.00%
Hepatotoxicity - 0.6201 62.01%
skin sensitisation + 0.7744 77.44%
Respiratory toxicity - 0.8889 88.89%
Reproductive toxicity - 0.5889 58.89%
Mitochondrial toxicity - 0.8625 86.25%
Nephrotoxicity - 0.7132 71.32%
Acute Oral Toxicity (c) III 0.7763 77.63%
Estrogen receptor binding + 0.8990 89.90%
Androgen receptor binding + 0.8178 81.78%
Thyroid receptor binding + 0.5816 58.16%
Glucocorticoid receptor binding + 0.6464 64.64%
Aromatase binding + 0.7991 79.91%
PPAR gamma + 0.8671 86.71%
Honey bee toxicity - 0.9269 92.69%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.6700 67.00%
Fish aquatic toxicity + 0.9143 91.43%

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 96.86% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.78% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.66% 86.33%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 93.07% 96.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 92.63% 93.99%
CHEMBL242 Q92731 Estrogen receptor beta 89.98% 98.35%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.20% 96.09%
CHEMBL2535 P11166 Glucose transporter 88.15% 98.75%
CHEMBL3194 P02766 Transthyretin 86.16% 90.71%
CHEMBL2581 P07339 Cathepsin D 86.09% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 86.07% 94.73%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 84.91% 91.71%
CHEMBL2146302 O94925 Glutaminase kidney isoform, mitochondrial 84.23% 100.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.56% 99.17%
CHEMBL4208 P20618 Proteasome component C5 82.89% 90.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 82.54% 99.15%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 82.35% 95.50%
CHEMBL2487 P05067 Beta amyloid A4 protein 80.21% 96.74%

Cross-Links

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PubChem 5469252
NPASS NPC12987