(E)-9-oxooctadec-10-enoic Acid

Details

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Internal ID 8c05389a-bd0a-43e0-a325-27da6e557f26
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Lineolic acids and derivatives
IUPAC Name (E)-9-oxooctadec-10-enoic acid
SMILES (Canonical) CCCCCCCC=CC(=O)CCCCCCCC(=O)O
SMILES (Isomeric) CCCCCCC/C=C/C(=O)CCCCCCCC(=O)O
InChI InChI=1S/C18H32O3/c1-2-3-4-5-6-8-11-14-17(19)15-12-9-7-10-13-16-18(20)21/h11,14H,2-10,12-13,15-16H2,1H3,(H,20,21)/b14-11+
InChI Key CCGQEYYMFYDMAX-SDNWHVSQSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C18H32O3
Molecular Weight 296.40 g/mol
Exact Mass 296.23514488 g/mol
Topological Polar Surface Area (TPSA) 54.40 Ų
XlogP 5.70
Atomic LogP (AlogP) 5.29
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 15

Synonyms

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Octadec-10-enoic acid, 9-oxo-, (E)-
99640-11-6
CHEMBL256146

2D Structure

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2D Structure of (E)-9-oxooctadec-10-enoic Acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9863 98.63%
Caco-2 + 0.6399 63.99%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability - 0.7857 78.57%
Subcellular localzation Mitochondria 0.7201 72.01%
OATP2B1 inhibitior - 0.8481 84.81%
OATP1B1 inhibitior + 0.7819 78.19%
OATP1B3 inhibitior + 0.8253 82.53%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.7635 76.35%
P-glycoprotein inhibitior - 0.8515 85.15%
P-glycoprotein substrate - 0.9457 94.57%
CYP3A4 substrate - 0.6276 62.76%
CYP2C9 substrate - 0.7659 76.59%
CYP2D6 substrate - 0.9025 90.25%
CYP3A4 inhibition - 0.8963 89.63%
CYP2C9 inhibition - 0.9213 92.13%
CYP2C19 inhibition - 0.9408 94.08%
CYP2D6 inhibition - 0.9466 94.66%
CYP1A2 inhibition + 0.6073 60.73%
CYP2C8 inhibition - 0.8618 86.18%
CYP inhibitory promiscuity - 0.9519 95.19%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7835 78.35%
Carcinogenicity (trinary) Non-required 0.7320 73.20%
Eye corrosion + 0.6925 69.25%
Eye irritation + 0.9099 90.99%
Skin irritation + 0.7030 70.30%
Skin corrosion - 0.5997 59.97%
Ames mutagenesis - 0.9600 96.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3733 37.33%
Micronuclear - 0.9700 97.00%
Hepatotoxicity - 0.7000 70.00%
skin sensitisation + 0.5359 53.59%
Respiratory toxicity - 0.6778 67.78%
Reproductive toxicity - 0.8522 85.22%
Mitochondrial toxicity - 0.5250 52.50%
Nephrotoxicity - 0.7165 71.65%
Acute Oral Toxicity (c) III 0.5383 53.83%
Estrogen receptor binding - 0.5585 55.85%
Androgen receptor binding - 0.7905 79.05%
Thyroid receptor binding + 0.5781 57.81%
Glucocorticoid receptor binding - 0.5828 58.28%
Aromatase binding - 0.8169 81.69%
PPAR gamma + 0.6151 61.51%
Honey bee toxicity - 0.9916 99.16%
Biodegradation + 0.9000 90.00%
Crustacea aquatic toxicity + 0.8600 86.00%
Fish aquatic toxicity + 0.9708 97.08%

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
CHEMBL230 P35354 Cyclooxygenase-2 98.97% 89.63%
CHEMBL3060 Q9Y345 Glycine transporter 2 98.03% 99.17%
CHEMBL2581 P07339 Cathepsin D 95.74% 98.95%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 94.11% 92.08%
CHEMBL221 P23219 Cyclooxygenase-1 93.03% 90.17%
CHEMBL1781 P11387 DNA topoisomerase I 91.90% 97.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.34% 96.09%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 85.40% 97.29%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 84.86% 96.95%
CHEMBL2001 Q9H244 Purinergic receptor P2Y12 84.78% 96.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.37% 91.11%
CHEMBL5285 Q99683 Mitogen-activated protein kinase kinase kinase 5 82.34% 92.26%
CHEMBL5255 O00206 Toll-like receptor 4 80.11% 92.50%

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.
Galeopsis bifida

Cross-Links

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PubChem 6443258
LOTUS LTS0240955
wikiData Q104953296