3-(4-Hydroxyphenyl)prop-2-enyl octadeca-9,12-dienoate

Details

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Internal ID d33ff787-77ca-41b5-818c-490e8f864cd6
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Lineolic acids and derivatives
IUPAC Name 3-(4-hydroxyphenyl)prop-2-enyl octadeca-9,12-dienoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C27H40O3/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-19-27(29)30-24-17-18-25-20-22-26(28)23-21-25/h6-7,9-10,17-18,20-23,28H,2-5,8,11-16,19,24H2,1H3
InChI Key HGWQWDQGDCAJEH-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C27H40O3
Molecular Weight 412.60 g/mol
Exact Mass 412.29774513 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 8.70
Atomic LogP (AlogP) 7.76
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 17

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3-(4-Hydroxyphenyl)prop-2-enyl octadeca-9,12-dienoate

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 - 0.6237 62.37%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability - 0.8000 80.00%
Subcellular localzation Mitochondria 0.6896 68.96%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior - 0.3276 32.76%
OATP1B3 inhibitior + 0.9282 92.82%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.9233 92.33%
P-glycoprotein inhibitior + 0.6646 66.46%
P-glycoprotein substrate - 0.8396 83.96%
CYP3A4 substrate + 0.5435 54.35%
CYP2C9 substrate - 0.8027 80.27%
CYP2D6 substrate - 0.8420 84.20%
CYP3A4 inhibition - 0.7322 73.22%
CYP2C9 inhibition - 0.8905 89.05%
CYP2C19 inhibition + 0.6531 65.31%
CYP2D6 inhibition - 0.8436 84.36%
CYP1A2 inhibition + 0.7271 72.71%
CYP2C8 inhibition + 0.7448 74.48%
CYP inhibitory promiscuity - 0.7184 71.84%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.8023 80.23%
Carcinogenicity (trinary) Non-required 0.6570 65.70%
Eye corrosion - 0.9661 96.61%
Eye irritation - 0.7105 71.05%
Skin irritation - 0.7872 78.72%
Skin corrosion - 0.9847 98.47%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3621 36.21%
Micronuclear - 0.9700 97.00%
Hepatotoxicity + 0.5159 51.59%
skin sensitisation + 0.4849 48.49%
Respiratory toxicity - 0.8111 81.11%
Reproductive toxicity - 0.8179 81.79%
Mitochondrial toxicity - 0.9750 97.50%
Nephrotoxicity - 0.5949 59.49%
Acute Oral Toxicity (c) III 0.6434 64.34%
Estrogen receptor binding + 0.7845 78.45%
Androgen receptor binding - 0.4815 48.15%
Thyroid receptor binding - 0.5352 53.52%
Glucocorticoid receptor binding + 0.5937 59.37%
Aromatase binding - 0.5131 51.31%
PPAR gamma - 0.6153 61.53%
Honey bee toxicity - 0.9642 96.42%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity + 0.8878 88.78%
Fish aquatic toxicity + 0.9948 99.48%

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 98.86% 99.17%
CHEMBL2581 P07339 Cathepsin D 96.45% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.22% 96.09%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 91.87% 96.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.83% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.62% 86.33%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 91.22% 92.08%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 90.24% 91.71%
CHEMBL230 P35354 Cyclooxygenase-2 88.17% 89.63%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.78% 95.56%
CHEMBL4227 P25090 Lipoxin A4 receptor 82.09% 100.00%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 81.53% 100.00%
CHEMBL242 Q92731 Estrogen receptor beta 81.00% 98.35%
CHEMBL3194 P02766 Transthyretin 80.80% 90.71%
CHEMBL3401 O75469 Pregnane X receptor 80.69% 94.73%

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.
Cydonia oblonga

Cross-Links

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PubChem 163000064
LOTUS LTS0068324
wikiData Q105028012