3-Heptadeca-8,11,14-trienyl-5-methoxyphenol

Details

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Internal ID 80c28a08-f856-4a32-a0f5-bbebef9e0edd
Taxonomy Benzenoids > Phenols > Methoxyphenols
IUPAC Name 3-heptadeca-8,11,14-trienyl-5-methoxyphenol
SMILES (Canonical) CCC=CCC=CCC=CCCCCCCCC1=CC(=CC(=C1)OC)O
SMILES (Isomeric) CCC=CCC=CCC=CCCCCCCCC1=CC(=CC(=C1)OC)O
InChI InChI=1S/C24H36O2/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-22-19-23(25)21-24(20-22)26-2/h4-5,7-8,10-11,19-21,25H,3,6,9,12-18H2,1-2H3
InChI Key QSAZGMNPQJKWDO-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C24H36O2
Molecular Weight 356.50 g/mol
Exact Mass 356.271530387 g/mol
Topological Polar Surface Area (TPSA) 29.50 Ų
XlogP 8.20
Atomic LogP (AlogP) 7.14
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 14

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3-Heptadeca-8,11,14-trienyl-5-methoxyphenol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9945 99.45%
Caco-2 - 0.5155 51.55%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability - 0.7571 75.71%
Subcellular localzation Mitochondria 0.7371 73.71%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior - 0.3182 31.82%
OATP1B3 inhibitior + 0.9401 94.01%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.9259 92.59%
P-glycoprotein inhibitior + 0.8214 82.14%
P-glycoprotein substrate - 0.7320 73.20%
CYP3A4 substrate + 0.5362 53.62%
CYP2C9 substrate + 0.6000 60.00%
CYP2D6 substrate + 0.3925 39.25%
CYP3A4 inhibition - 0.7477 74.77%
CYP2C9 inhibition - 0.8356 83.56%
CYP2C19 inhibition + 0.5513 55.13%
CYP2D6 inhibition - 0.8278 82.78%
CYP1A2 inhibition + 0.6186 61.86%
CYP2C8 inhibition + 0.6837 68.37%
CYP inhibitory promiscuity + 0.6531 65.31%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.6675 66.75%
Carcinogenicity (trinary) Non-required 0.6416 64.16%
Eye corrosion - 0.6858 68.58%
Eye irritation - 0.7167 71.67%
Skin irritation - 0.5737 57.37%
Skin corrosion - 0.8964 89.64%
Ames mutagenesis - 0.7200 72.00%
Human Ether-a-go-go-Related Gene inhibition + 0.9091 90.91%
Micronuclear - 0.9300 93.00%
Hepatotoxicity - 0.7717 77.17%
skin sensitisation + 0.7561 75.61%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity - 0.5047 50.47%
Mitochondrial toxicity - 0.8500 85.00%
Nephrotoxicity - 0.8371 83.71%
Acute Oral Toxicity (c) III 0.8582 85.82%
Estrogen receptor binding + 0.8825 88.25%
Androgen receptor binding + 0.5425 54.25%
Thyroid receptor binding + 0.6488 64.88%
Glucocorticoid receptor binding + 0.7241 72.41%
Aromatase binding - 0.5000 50.00%
PPAR gamma + 0.6261 62.61%
Honey bee toxicity - 0.9351 93.51%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity + 0.6662 66.62%
Fish aquatic toxicity + 0.9242 92.42%

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
CHEMBL3060 Q9Y345 Glycine transporter 2 97.21% 99.17%
CHEMBL2581 P07339 Cathepsin D 96.19% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.48% 96.09%
CHEMBL239 Q07869 Peroxisome proliferator-activated receptor alpha 95.44% 90.75%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.88% 91.11%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 90.75% 92.08%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 89.91% 92.68%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.87% 86.33%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 85.58% 96.95%
CHEMBL4208 P20618 Proteasome component C5 84.00% 90.00%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 83.72% 91.71%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.19% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 82.59% 94.73%
CHEMBL2535 P11166 Glucose transporter 81.67% 98.75%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.73% 94.45%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 80.37% 97.29%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 80.13% 95.89%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 162956802
LOTUS LTS0243313
wikiData Q105226835