2-Butoxyethyl linolenate

Details

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Internal ID d4579f5e-cff3-47fd-b41b-e34395868bd1
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Lineolic acids and derivatives
IUPAC Name 2-butoxyethyl (9Z,12Z,15Z)-octadeca-9,12,15-trienoate
SMILES (Canonical) CCCCOCCOC(=O)CCCCCCCC=CCC=CCC=CCC
SMILES (Isomeric) CCCCOCCOC(=O)CCCCCCC/C=C\C/C=C\C/C=C\CC
InChI InChI=1S/C24H42O3/c1-3-5-7-8-9-10-11-12-13-14-15-16-17-18-19-20-24(25)27-23-22-26-21-6-4-2/h5,7,9-10,12-13H,3-4,6,8,11,14-23H2,1-2H3/b7-5-,10-9-,13-12-
InChI Key TVFKGQZWJHZMNC-XQOKXTRKSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C24H42O3
Molecular Weight 378.60 g/mol
Exact Mass 378.31339520 g/mol
Topological Polar Surface Area (TPSA) 35.50 Ų
XlogP 7.30
Atomic LogP (AlogP) 6.94
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 19

Synonyms

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SCHEMBL3653963

2D Structure

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2D Structure of 2-Butoxyethyl linolenate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9900 99.00%
Caco-2 + 0.5888 58.88%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Mitochondria 0.4527 45.27%
OATP2B1 inhibitior - 0.8544 85.44%
OATP1B1 inhibitior - 0.3884 38.84%
OATP1B3 inhibitior + 0.9224 92.24%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.8528 85.28%
P-glycoprotein inhibitior - 0.5226 52.26%
P-glycoprotein substrate - 0.8557 85.57%
CYP3A4 substrate + 0.5752 57.52%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8693 86.93%
CYP3A4 inhibition - 0.9456 94.56%
CYP2C9 inhibition - 0.9361 93.61%
CYP2C19 inhibition - 0.9177 91.77%
CYP2D6 inhibition - 0.9210 92.10%
CYP1A2 inhibition - 0.7289 72.89%
CYP2C8 inhibition - 0.5736 57.36%
CYP inhibitory promiscuity - 0.8793 87.93%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6823 68.23%
Carcinogenicity (trinary) Non-required 0.6261 62.61%
Eye corrosion + 0.8820 88.20%
Eye irritation - 0.5298 52.98%
Skin irritation - 0.7310 73.10%
Skin corrosion - 0.9806 98.06%
Ames mutagenesis - 0.7632 76.32%
Human Ether-a-go-go-Related Gene inhibition - 0.3661 36.61%
Micronuclear - 0.9800 98.00%
Hepatotoxicity - 0.6289 62.89%
skin sensitisation - 0.5778 57.78%
Respiratory toxicity - 0.7889 78.89%
Reproductive toxicity - 0.7778 77.78%
Mitochondrial toxicity - 1.0000 100.00%
Nephrotoxicity - 0.7449 74.49%
Acute Oral Toxicity (c) III 0.5264 52.64%
Estrogen receptor binding + 0.6281 62.81%
Androgen receptor binding - 0.7983 79.83%
Thyroid receptor binding + 0.5207 52.07%
Glucocorticoid receptor binding - 0.6140 61.40%
Aromatase binding - 0.6595 65.95%
PPAR gamma - 0.5844 58.44%
Honey bee toxicity - 0.9757 97.57%
Biodegradation + 0.6000 60.00%
Crustacea aquatic toxicity + 0.7324 73.24%
Fish aquatic toxicity + 0.9620 96.20%

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 98.70% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.73% 96.09%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 94.56% 85.94%
CHEMBL2581 P07339 Cathepsin D 93.80% 98.95%
CHEMBL239 Q07869 Peroxisome proliferator-activated receptor alpha 92.30% 90.75%
CHEMBL1907 P15144 Aminopeptidase N 86.98% 93.31%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.79% 91.11%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 85.35% 92.08%
CHEMBL2664 P23526 Adenosylhomocysteinase 84.95% 86.67%
CHEMBL5255 O00206 Toll-like receptor 4 84.66% 92.50%
CHEMBL1781 P11387 DNA topoisomerase I 83.30% 97.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.28% 86.33%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 83.23% 94.33%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 83.04% 100.00%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 82.87% 97.29%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.04% 96.00%
CHEMBL221 P23219 Cyclooxygenase-1 81.60% 90.17%
CHEMBL230 P35354 Cyclooxygenase-2 81.11% 89.63%
CHEMBL3004 P33527 Multidrug resistance-associated protein 1 80.52% 96.37%

Cross-Links

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PubChem 87552578
NPASS NPC227930
LOTUS LTS0196378
wikiData Q105265238