(9E,11Z,13S,15Z)-13-hydroperoxyoctadeca-9,11,15-trienoic acid

Details

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Internal ID d9d72af7-e956-40a7-8a20-e65024ed9514
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Lineolic acids and derivatives
IUPAC Name (9E,11Z,13S,15Z)-13-hydroperoxyoctadeca-9,11,15-trienoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C18H30O4/c1-2-3-11-14-17(22-21)15-12-9-7-5-4-6-8-10-13-16-18(19)20/h3,7,9,11-12,15,17,21H,2,4-6,8,10,13-14,16H2,1H3,(H,19,20)/b9-7+,11-3-,15-12-/t17-/m0/s1
InChI Key UYQGVDXDXBAABN-XICOYCALSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C18H30O4
Molecular Weight 310.40 g/mol
Exact Mass 310.21440943 g/mol
Topological Polar Surface Area (TPSA) 66.80 Ų
XlogP 4.80
Atomic LogP (AlogP) 5.13
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 14

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (9E,11Z,13S,15Z)-13-hydroperoxyoctadeca-9,11,15-trienoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8983 89.83%
Caco-2 - 0.5731 57.31%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability - 0.7429 74.29%
Subcellular localzation Mitochondria 0.7485 74.85%
OATP2B1 inhibitior - 0.8546 85.46%
OATP1B1 inhibitior + 0.8026 80.26%
OATP1B3 inhibitior + 0.9237 92.37%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.5000 50.00%
P-glycoprotein inhibitior - 0.6703 67.03%
P-glycoprotein substrate - 0.8749 87.49%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 0.5853 58.53%
CYP2D6 substrate - 0.8797 87.97%
CYP3A4 inhibition - 0.9272 92.72%
CYP2C9 inhibition - 0.8864 88.64%
CYP2C19 inhibition - 0.8965 89.65%
CYP2D6 inhibition - 0.9243 92.43%
CYP1A2 inhibition - 0.7572 75.72%
CYP2C8 inhibition - 0.7630 76.30%
CYP inhibitory promiscuity - 0.8700 87.00%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.6235 62.35%
Carcinogenicity (trinary) Non-required 0.6684 66.84%
Eye corrosion - 0.7103 71.03%
Eye irritation - 0.7456 74.56%
Skin irritation - 0.7728 77.28%
Skin corrosion - 0.7764 77.64%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7124 71.24%
Micronuclear - 0.8700 87.00%
Hepatotoxicity - 0.5196 51.96%
skin sensitisation - 0.6127 61.27%
Respiratory toxicity + 0.6889 68.89%
Reproductive toxicity - 0.8255 82.55%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity - 0.8101 81.01%
Acute Oral Toxicity (c) III 0.5208 52.08%
Estrogen receptor binding + 0.7113 71.13%
Androgen receptor binding - 0.6836 68.36%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding - 0.6368 63.68%
Aromatase binding - 0.5300 53.00%
PPAR gamma + 0.8039 80.39%
Honey bee toxicity - 0.9054 90.54%
Biodegradation + 0.5500 55.00%
Crustacea aquatic toxicity + 0.5700 57.00%
Fish aquatic toxicity + 0.8760 87.60%

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 97.89% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.35% 96.09%
CHEMBL2581 P07339 Cathepsin D 95.45% 98.95%
CHEMBL5285 Q99683 Mitogen-activated protein kinase kinase kinase 5 89.15% 92.26%
CHEMBL1781 P11387 DNA topoisomerase I 85.46% 97.00%
CHEMBL3359 P21462 Formyl peptide receptor 1 85.44% 93.56%
CHEMBL221 P23219 Cyclooxygenase-1 84.29% 90.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.88% 91.11%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.58% 96.95%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.40% 96.00%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 82.42% 97.29%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 81.59% 100.00%
CHEMBL2072 P35499 Sodium channel protein type IV alpha subunit 81.21% 92.32%

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 163000024
LOTUS LTS0102144
wikiData Q105281827