9,16-Dioxooctadec-10,12,14-trienoic acid

Details

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Internal ID 9e3e6e8e-15ec-49b3-ad9f-20e2e8bb2024
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Lineolic acids and derivatives
IUPAC Name 9,16-dioxooctadeca-10,12,14-trienoic acid
SMILES (Canonical) CCC(=O)C=CC=CC=CC(=O)CCCCCCCC(=O)O
SMILES (Isomeric) CCC(=O)C=CC=CC=CC(=O)CCCCCCCC(=O)O
InChI InChI=1S/C18H26O4/c1-2-16(19)12-8-6-7-10-14-17(20)13-9-4-3-5-11-15-18(21)22/h6-8,10,12,14H,2-5,9,11,13,15H2,1H3,(H,21,22)
InChI Key PQPRTPXWQQQKJC-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C18H26O4
Molecular Weight 306.40 g/mol
Exact Mass 306.18310931 g/mol
Topological Polar Surface Area (TPSA) 71.40 Ų
XlogP 3.40
Atomic LogP (AlogP) 4.02
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 13

Synonyms

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9,16-dioxooctadec-10,12,14-trienoic acid

2D Structure

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2D Structure of 9,16-Dioxooctadec-10,12,14-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 + 0.9458 94.58%
Caco-2 - 0.5345 53.45%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.8445 84.45%
OATP2B1 inhibitior - 0.8586 85.86%
OATP1B1 inhibitior + 0.9150 91.50%
OATP1B3 inhibitior + 0.9286 92.86%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.4716 47.16%
P-glycoprotein inhibitior - 0.7550 75.50%
P-glycoprotein substrate - 0.9490 94.90%
CYP3A4 substrate - 0.6251 62.51%
CYP2C9 substrate - 0.7659 76.59%
CYP2D6 substrate - 0.9025 90.25%
CYP3A4 inhibition - 0.9255 92.55%
CYP2C9 inhibition - 0.9125 91.25%
CYP2C19 inhibition - 0.9440 94.40%
CYP2D6 inhibition - 0.9508 95.08%
CYP1A2 inhibition - 0.8070 80.70%
CYP2C8 inhibition - 0.8784 87.84%
CYP inhibitory promiscuity - 0.9707 97.07%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7735 77.35%
Carcinogenicity (trinary) Non-required 0.7436 74.36%
Eye corrosion + 0.5567 55.67%
Eye irritation - 0.5275 52.75%
Skin irritation - 0.5291 52.91%
Skin corrosion - 0.8389 83.89%
Ames mutagenesis - 0.8700 87.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6891 68.91%
Micronuclear - 0.9800 98.00%
Hepatotoxicity - 0.5875 58.75%
skin sensitisation - 0.6999 69.99%
Respiratory toxicity + 0.6889 68.89%
Reproductive toxicity - 0.8438 84.38%
Mitochondrial toxicity + 0.8000 80.00%
Nephrotoxicity - 0.7683 76.83%
Acute Oral Toxicity (c) III 0.5926 59.26%
Estrogen receptor binding + 0.7427 74.27%
Androgen receptor binding - 0.8516 85.16%
Thyroid receptor binding - 0.4922 49.22%
Glucocorticoid receptor binding - 0.4907 49.07%
Aromatase binding + 0.6737 67.37%
PPAR gamma + 0.6589 65.89%
Honey bee toxicity - 0.9827 98.27%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.8649 86.49%

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 94.41% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.56% 96.09%
CHEMBL2581 P07339 Cathepsin D 91.63% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.61% 91.11%
CHEMBL230 P35354 Cyclooxygenase-2 90.32% 89.63%
CHEMBL221 P23219 Cyclooxygenase-1 85.64% 90.17%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.61% 96.95%
CHEMBL1781 P11387 DNA topoisomerase I 80.06% 97.00%

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.
Helianthus hirsutus
Sorghum bicolor

Cross-Links

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PubChem 73450242
NPASS NPC159952
LOTUS LTS0143623
wikiData Q105213338