(10E,14Z)-9-oxooctadeca-10,14-dien-12-ynoic acid

Details

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Internal ID 873e0b64-7cd9-49e6-a332-1da4a7ea4467
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acids and conjugates > Long-chain fatty acids
IUPAC Name (10E,14Z)-9-oxooctadeca-10,14-dien-12-ynoic acid
SMILES (Canonical) CCCC=CC#CC=CC(=O)CCCCCCCC(=O)O
SMILES (Isomeric) CCC/C=C\C#C/C=C/C(=O)CCCCCCCC(=O)O
InChI InChI=1S/C18H26O3/c1-2-3-4-5-6-8-11-14-17(19)15-12-9-7-10-13-16-18(20)21/h4-5,11,14H,2-3,7,9-10,12-13,15-16H2,1H3,(H,20,21)/b5-4-,14-11+
InChI Key SNUNXDVKYBQMPJ-UZWKOAOVSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C18H26O3
Molecular Weight 290.40 g/mol
Exact Mass 290.18819469 g/mol
Topological Polar Surface Area (TPSA) 54.40 Ų
XlogP 4.60
Atomic LogP (AlogP) 4.29
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 11

Synonyms

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SCHEMBL20548572
BDBM50365803

2D Structure

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2D Structure of (10E,14Z)-9-oxooctadeca-10,14-dien-12-ynoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9757 97.57%
Caco-2 - 0.5584 55.84%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.7000 70.00%
Subcellular localzation Mitochondria 0.7060 70.60%
OATP2B1 inhibitior - 0.8534 85.34%
OATP1B1 inhibitior + 0.8570 85.70%
OATP1B3 inhibitior + 0.8962 89.62%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.7338 73.38%
P-glycoprotein inhibitior - 0.7978 79.78%
P-glycoprotein substrate - 0.9171 91.71%
CYP3A4 substrate - 0.5496 54.96%
CYP2C9 substrate - 0.7887 78.87%
CYP2D6 substrate - 0.8850 88.50%
CYP3A4 inhibition - 0.8360 83.60%
CYP2C9 inhibition - 0.8289 82.89%
CYP2C19 inhibition - 0.8879 88.79%
CYP2D6 inhibition - 0.9428 94.28%
CYP1A2 inhibition + 0.5172 51.72%
CYP2C8 inhibition - 0.8034 80.34%
CYP inhibitory promiscuity - 0.9347 93.47%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7235 72.35%
Carcinogenicity (trinary) Non-required 0.6787 67.87%
Eye corrosion + 0.5923 59.23%
Eye irritation - 0.7713 77.13%
Skin irritation + 0.6213 62.13%
Skin corrosion - 0.5304 53.04%
Ames mutagenesis - 0.9100 91.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3871 38.71%
Micronuclear - 0.9300 93.00%
Hepatotoxicity - 0.7000 70.00%
skin sensitisation + 0.5375 53.75%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity - 0.8057 80.57%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity - 0.6994 69.94%
Acute Oral Toxicity (c) II 0.4189 41.89%
Estrogen receptor binding - 0.4764 47.64%
Androgen receptor binding - 0.8470 84.70%
Thyroid receptor binding + 0.5820 58.20%
Glucocorticoid receptor binding + 0.6694 66.94%
Aromatase binding - 0.6193 61.93%
PPAR gamma + 0.6320 63.20%
Honey bee toxicity - 0.9652 96.52%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity + 0.5500 55.00%
Fish aquatic toxicity + 0.9444 94.44%

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 95.71% 99.17%
CHEMBL230 P35354 Cyclooxygenase-2 93.77% 89.63%
CHEMBL221 P23219 Cyclooxygenase-1 92.21% 90.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.03% 96.09%
CHEMBL2581 P07339 Cathepsin D 91.07% 98.95%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 87.08% 92.08%
CHEMBL1781 P11387 DNA topoisomerase I 86.75% 97.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.01% 91.11%
CHEMBL4040 P28482 MAP kinase ERK2 82.57% 83.82%
CHEMBL5285 Q99683 Mitogen-activated protein kinase kinase kinase 5 82.40% 92.26%
CHEMBL5255 O00206 Toll-like receptor 4 80.89% 92.50%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.74% 96.95%

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 57345550
LOTUS LTS0164180
wikiData Q105256690