4-Oct-3-enylphenol

Details

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Internal ID edd129d9-5ce6-4e4f-8c47-c14183a943ae
Taxonomy Benzenoids > Phenols > 1-hydroxy-2-unsubstituted benzenoids
IUPAC Name 4-oct-3-enylphenol
SMILES (Canonical) CCCCC=CCCC1=CC=C(C=C1)O
SMILES (Isomeric) CCCCC=CCCC1=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/h5-6,9-12,15H,2-4,7-8H2,1H3
InChI Key UTXMWVVQOZAGKZ-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 4.70
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-3-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 + 0.9642 96.42%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability - 0.7857 78.57%
Subcellular localzation Plasma membrane 0.4545 45.45%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior - 0.3350 33.50%
OATP1B3 inhibitior + 0.9558 95.58%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.6518 65.18%
P-glycoprotein inhibitior - 0.9726 97.26%
P-glycoprotein substrate - 0.7382 73.82%
CYP3A4 substrate - 0.6101 61.01%
CYP2C9 substrate - 0.7928 79.28%
CYP2D6 substrate + 0.3567 35.67%
CYP3A4 inhibition - 0.7074 70.74%
CYP2C9 inhibition - 0.8121 81.21%
CYP2C19 inhibition - 0.6217 62.17%
CYP2D6 inhibition - 0.8964 89.64%
CYP1A2 inhibition + 0.7397 73.97%
CYP2C8 inhibition + 0.6430 64.30%
CYP inhibitory promiscuity + 0.5000 50.00%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.7211 72.11%
Carcinogenicity (trinary) Non-required 0.6586 65.86%
Eye corrosion + 0.9553 95.53%
Eye irritation + 0.9764 97.64%
Skin irritation + 0.7664 76.64%
Skin corrosion + 0.8068 80.68%
Ames mutagenesis - 0.8600 86.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5961 59.61%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.5625 56.25%
skin sensitisation + 0.9552 95.52%
Respiratory toxicity - 0.7000 70.00%
Reproductive toxicity - 0.5075 50.75%
Mitochondrial toxicity - 0.9000 90.00%
Nephrotoxicity - 0.6874 68.74%
Acute Oral Toxicity (c) III 0.8709 87.09%
Estrogen receptor binding + 0.5860 58.60%
Androgen receptor binding - 0.4819 48.19%
Thyroid receptor binding + 0.6134 61.34%
Glucocorticoid receptor binding - 0.7757 77.57%
Aromatase binding - 0.5109 51.09%
PPAR gamma + 0.8052 80.52%
Honey bee toxicity - 0.9828 98.28%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.6832 68.32%
Fish aquatic toxicity + 0.9925 99.25%

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
CHEMBL2581 P07339 Cathepsin D 96.91% 98.95%
CHEMBL242 Q92731 Estrogen receptor beta 96.37% 98.35%
CHEMBL3060 Q9Y345 Glycine transporter 2 94.62% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.66% 96.09%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 90.01% 92.08%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.08% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.30% 86.33%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 85.85% 100.00%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 84.68% 96.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.59% 94.45%
CHEMBL2996 Q05655 Protein kinase C delta 82.01% 97.79%
CHEMBL3401 O75469 Pregnane X receptor 80.84% 94.73%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 80.67% 91.71%

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 86035163
LOTUS LTS0060602
wikiData Q105279170