Methyl 18-methyl-19-oxoicosa-2,5,7,9,11,13,15,17-octaenoate

Details

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Internal ID 6d3513d3-b5f2-4946-ae55-4926892db934
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acid esters
IUPAC Name methyl 18-methyl-19-oxoicosa-2,5,7,9,11,13,15,17-octaenoate
SMILES (Canonical) CC(=CC=CC=CC=CC=CC=CC=CCC=CC(=O)OC)C(=O)C
SMILES (Isomeric) CC(=CC=CC=CC=CC=CC=CC=CCC=CC(=O)OC)C(=O)C
InChI InChI=1S/C22H26O3/c1-20(21(2)23)18-16-14-12-10-8-6-4-5-7-9-11-13-15-17-19-22(24)25-3/h4-14,16-19H,15H2,1-3H3
InChI Key XMMMGDYSHVKTBJ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C22H26O3
Molecular Weight 338.40 g/mol
Exact Mass 338.18819469 g/mol
Topological Polar Surface Area (TPSA) 43.40 Ų
XlogP 5.20
Atomic LogP (AlogP) 4.98
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 10

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Methyl 18-methyl-19-oxoicosa-2,5,7,9,11,13,15,17-octaenoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9876 98.76%
Caco-2 + 0.5912 59.12%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.8041 80.41%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8795 87.95%
OATP1B3 inhibitior + 0.9540 95.40%
MATE1 inhibitior - 0.7400 74.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.8598 85.98%
P-glycoprotein inhibitior - 0.6121 61.21%
P-glycoprotein substrate - 0.9159 91.59%
CYP3A4 substrate - 0.5213 52.13%
CYP2C9 substrate - 0.7947 79.47%
CYP2D6 substrate - 0.8998 89.98%
CYP3A4 inhibition - 0.9479 94.79%
CYP2C9 inhibition - 0.9116 91.16%
CYP2C19 inhibition - 0.9004 90.04%
CYP2D6 inhibition - 0.9526 95.26%
CYP1A2 inhibition - 0.9283 92.83%
CYP2C8 inhibition - 0.8800 88.00%
CYP inhibitory promiscuity - 0.6883 68.83%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5971 59.71%
Carcinogenicity (trinary) Non-required 0.6425 64.25%
Eye corrosion + 0.7067 70.67%
Eye irritation - 0.8172 81.72%
Skin irritation + 0.6079 60.79%
Skin corrosion - 0.9598 95.98%
Ames mutagenesis - 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8825 88.25%
Micronuclear - 0.7941 79.41%
Hepatotoxicity - 0.5224 52.24%
skin sensitisation + 0.8720 87.20%
Respiratory toxicity - 0.7111 71.11%
Reproductive toxicity - 0.9111 91.11%
Mitochondrial toxicity - 0.8500 85.00%
Nephrotoxicity + 0.6815 68.15%
Acute Oral Toxicity (c) III 0.7212 72.12%
Estrogen receptor binding + 0.7506 75.06%
Androgen receptor binding - 0.7514 75.14%
Thyroid receptor binding + 0.5430 54.30%
Glucocorticoid receptor binding + 0.6114 61.14%
Aromatase binding + 0.6651 66.51%
PPAR gamma + 0.5551 55.51%
Honey bee toxicity - 0.8276 82.76%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.7612 76.12%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.68% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.78% 91.11%
CHEMBL4040 P28482 MAP kinase ERK2 89.53% 83.82%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.49% 99.17%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 83.77% 89.34%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 83.03% 94.33%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.56% 96.00%

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 163063183
LOTUS LTS0001316
wikiData Q105331223