Methyl 10-methoxy-8-oxooctadec-9-enoate

Details

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Internal ID 96f574d1-499f-4732-ba10-d2507977d57c
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Lineolic acids and derivatives
IUPAC Name methyl 10-methoxy-8-oxooctadec-9-enoate
SMILES (Canonical) CCCCCCCCC(=CC(=O)CCCCCCC(=O)OC)OC
SMILES (Isomeric) CCCCCCCCC(=CC(=O)CCCCCCC(=O)OC)OC
InChI InChI=1S/C20H36O4/c1-4-5-6-7-8-12-15-19(23-2)17-18(21)14-11-9-10-13-16-20(22)24-3/h17H,4-16H2,1-3H3
InChI Key YJUGEDOVVZWVQY-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C20H36O4
Molecular Weight 340.50 g/mol
Exact Mass 340.26135963 g/mol
Topological Polar Surface Area (TPSA) 52.60 Ų
XlogP 5.60
Atomic LogP (AlogP) 5.35
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 16

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Methyl 10-methoxy-8-oxooctadec-9-enoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9829 98.29%
Caco-2 + 0.8749 87.49%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability - 0.7286 72.86%
Subcellular localzation Mitochondria 0.6707 67.07%
OATP2B1 inhibitior - 0.8500 85.00%
OATP1B1 inhibitior + 0.9100 91.00%
OATP1B3 inhibitior + 0.9489 94.89%
MATE1 inhibitior - 0.5800 58.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.7933 79.33%
P-glycoprotein inhibitior - 0.4628 46.28%
P-glycoprotein substrate - 0.8306 83.06%
CYP3A4 substrate - 0.5382 53.82%
CYP2C9 substrate - 0.5733 57.33%
CYP2D6 substrate - 0.8912 89.12%
CYP3A4 inhibition - 0.8993 89.93%
CYP2C9 inhibition - 0.8832 88.32%
CYP2C19 inhibition - 0.7995 79.95%
CYP2D6 inhibition - 0.9444 94.44%
CYP1A2 inhibition - 0.7832 78.32%
CYP2C8 inhibition - 0.8152 81.52%
CYP inhibitory promiscuity - 0.7994 79.94%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6023 60.23%
Carcinogenicity (trinary) Non-required 0.6764 67.64%
Eye corrosion - 0.7451 74.51%
Eye irritation + 0.7737 77.37%
Skin irritation - 0.7578 75.78%
Skin corrosion - 0.9897 98.97%
Ames mutagenesis - 0.9400 94.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4628 46.28%
Micronuclear - 0.9400 94.00%
Hepatotoxicity - 0.5359 53.59%
skin sensitisation - 0.8967 89.67%
Respiratory toxicity - 0.9222 92.22%
Reproductive toxicity - 0.9778 97.78%
Mitochondrial toxicity - 0.8875 88.75%
Nephrotoxicity + 0.6124 61.24%
Acute Oral Toxicity (c) III 0.6159 61.59%
Estrogen receptor binding - 0.7239 72.39%
Androgen receptor binding - 0.6399 63.99%
Thyroid receptor binding - 0.5669 56.69%
Glucocorticoid receptor binding - 0.6108 61.08%
Aromatase binding - 0.8063 80.63%
PPAR gamma - 0.5752 57.52%
Honey bee toxicity - 0.9630 96.30%
Biodegradation + 0.6750 67.50%
Crustacea aquatic toxicity + 0.8693 86.93%
Fish aquatic toxicity + 0.9779 97.79%

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 98.90% 89.63%
CHEMBL3060 Q9Y345 Glycine transporter 2 97.69% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.75% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.10% 91.11%
CHEMBL2581 P07339 Cathepsin D 92.05% 98.95%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 91.40% 92.08%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 90.98% 97.29%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 89.43% 96.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.63% 94.45%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 85.85% 89.34%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 85.32% 94.33%
CHEMBL256 P0DMS8 Adenosine A3 receptor 84.65% 95.93%
CHEMBL299 P17252 Protein kinase C alpha 84.30% 98.03%
CHEMBL5255 O00206 Toll-like receptor 4 84.14% 92.50%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 83.02% 92.86%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.06% 96.00%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 81.57% 95.17%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 81.31% 91.81%
CHEMBL4227 P25090 Lipoxin A4 receptor 80.89% 100.00%
CHEMBL2664 P23526 Adenosylhomocysteinase 80.04% 86.67%
CHEMBL4374 Q9Y5X4 Photoreceptor-specific nuclear receptor 80.02% 85.00%

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.
Hibiscus rosa-sinensis

Cross-Links

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PubChem 162995324
LOTUS LTS0274589
wikiData Q105349484