4-Oct-4-enylphenol

Details

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Internal ID dc98c402-3b70-46ef-9dd4-ba6319d9702d
Taxonomy Benzenoids > Phenols > 1-hydroxy-2-unsubstituted benzenoids
IUPAC Name 4-oct-4-enylphenol
SMILES (Canonical) CCCC=CCCCC1=CC=C(C=C1)O
SMILES (Isomeric) CCCC=CCCCC1=CC=C(C=C1)O
InChI InChI=1S/C14H20O/c1-2-3-4-5-6-7-8-13-9-11-14(15)12-10-13/h4-5,9-12,15H,2-3,6-8H2,1H3
InChI Key WHTYMTFJEIRTRO-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C14H20O
Molecular Weight 204.31 g/mol
Exact Mass 204.151415257 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 5.00
Atomic LogP (AlogP) 4.07
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4-Oct-4-enylphenol

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 + 0.9670 96.70%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability - 0.7143 71.43%
Subcellular localzation Plasma membrane 0.4672 46.72%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior - 0.3642 36.42%
OATP1B3 inhibitior + 0.9555 95.55%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.6615 66.15%
P-glycoprotein inhibitior - 0.9604 96.04%
P-glycoprotein substrate - 0.7484 74.84%
CYP3A4 substrate - 0.5920 59.20%
CYP2C9 substrate - 0.7928 79.28%
CYP2D6 substrate + 0.3567 35.67%
CYP3A4 inhibition - 0.7553 75.53%
CYP2C9 inhibition - 0.8016 80.16%
CYP2C19 inhibition - 0.6591 65.91%
CYP2D6 inhibition - 0.9177 91.77%
CYP1A2 inhibition + 0.6313 63.13%
CYP2C8 inhibition + 0.6531 65.31%
CYP inhibitory promiscuity - 0.5078 50.78%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.6911 69.11%
Carcinogenicity (trinary) Non-required 0.6087 60.87%
Eye corrosion + 0.9613 96.13%
Eye irritation + 0.9809 98.09%
Skin irritation + 0.6365 63.65%
Skin corrosion + 0.6373 63.73%
Ames mutagenesis - 0.8600 86.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5236 52.36%
Micronuclear - 0.9441 94.41%
Hepatotoxicity - 0.7000 70.00%
skin sensitisation + 0.9560 95.60%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity - 0.5974 59.74%
Mitochondrial toxicity - 0.9000 90.00%
Nephrotoxicity - 0.7002 70.02%
Acute Oral Toxicity (c) III 0.8836 88.36%
Estrogen receptor binding + 0.5638 56.38%
Androgen receptor binding - 0.5000 50.00%
Thyroid receptor binding + 0.6400 64.00%
Glucocorticoid receptor binding - 0.7909 79.09%
Aromatase binding - 0.5544 55.44%
PPAR gamma + 0.7266 72.66%
Honey bee toxicity - 0.9648 96.48%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity + 0.6400 64.00%
Fish aquatic toxicity + 0.9824 98.24%

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 95.87% 98.35%
CHEMBL2581 P07339 Cathepsin D 95.45% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 93.09% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.93% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.25% 86.33%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 85.68% 91.71%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 85.22% 96.95%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 84.81% 100.00%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 84.69% 92.08%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.52% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 81.74% 94.73%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.93% 94.45%

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.
Piper gibbilimbum

Cross-Links

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PubChem 54431478
LOTUS LTS0213790
wikiData Q105305819