18-Methyl-19-oxoicosa-2,5,7,9,11,13,15,17-octaenoic acid

Details

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Internal ID 2ea507ab-132c-4856-9e74-dcbe48137fb0
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acids and conjugates > Long-chain fatty acids
IUPAC Name 18-methyl-19-oxoicosa-2,5,7,9,11,13,15,17-octaenoic acid
SMILES (Canonical) CC(=CC=CC=CC=CC=CC=CC=CCC=CC(=O)O)C(=O)C
SMILES (Isomeric) CC(=CC=CC=CC=CC=CC=CC=CCC=CC(=O)O)C(=O)C
InChI InChI=1S/C21H24O3/c1-19(20(2)22)17-15-13-11-9-7-5-3-4-6-8-10-12-14-16-18-21(23)24/h3-13,15-18H,14H2,1-2H3,(H,23,24)
InChI Key ZDCBICFDQMVGFI-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C21H24O3
Molecular Weight 324.40 g/mol
Exact Mass 324.17254462 g/mol
Topological Polar Surface Area (TPSA) 54.40 Ų
XlogP 4.90
Atomic LogP (AlogP) 4.89
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 10

Synonyms

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There are no found synonyms.

2D Structure

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

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9669 96.69%
Caco-2 + 0.5000 50.00%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.8526 85.26%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8769 87.69%
OATP1B3 inhibitior + 0.9553 95.53%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.8432 84.32%
P-glycoprotein inhibitior - 0.7978 79.78%
P-glycoprotein substrate - 0.9597 95.97%
CYP3A4 substrate - 0.6301 63.01%
CYP2C9 substrate - 0.7659 76.59%
CYP2D6 substrate - 0.9025 90.25%
CYP3A4 inhibition - 0.9058 90.58%
CYP2C9 inhibition - 0.8227 82.27%
CYP2C19 inhibition - 0.9117 91.17%
CYP2D6 inhibition - 0.9181 91.81%
CYP1A2 inhibition - 0.9629 96.29%
CYP2C8 inhibition - 0.9407 94.07%
CYP inhibitory promiscuity - 0.8786 87.86%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5365 53.65%
Carcinogenicity (trinary) Non-required 0.7042 70.42%
Eye corrosion + 0.8350 83.50%
Eye irritation - 0.7573 75.73%
Skin irritation + 0.8166 81.66%
Skin corrosion + 0.8340 83.40%
Ames mutagenesis - 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6431 64.31%
Micronuclear - 0.7341 73.41%
Hepatotoxicity + 0.5677 56.77%
skin sensitisation + 0.8015 80.15%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity - 0.7581 75.81%
Mitochondrial toxicity - 0.6000 60.00%
Nephrotoxicity + 0.6140 61.40%
Acute Oral Toxicity (c) III 0.7921 79.21%
Estrogen receptor binding + 0.6968 69.68%
Androgen receptor binding - 0.7198 71.98%
Thyroid receptor binding - 0.5375 53.75%
Glucocorticoid receptor binding - 0.5052 50.52%
Aromatase binding + 0.6943 69.43%
PPAR gamma + 0.6050 60.50%
Honey bee toxicity - 0.9223 92.23%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.6500 65.00%
Fish aquatic toxicity + 0.8029 80.29%

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 89.77% 96.09%
CHEMBL221 P23219 Cyclooxygenase-1 87.01% 90.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.69% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.47% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.44% 86.33%

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 163043570
LOTUS LTS0183295
wikiData Q105372052