1,2-Dioleoyl-3-linolein

Details

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Internal ID 47b92fd0-472d-46a7-93d7-242ab430b67b
Taxonomy Lipids and lipid-like molecules > Glycerolipids > Triradylcglycerols > Triacylglycerols
IUPAC Name [3-[(9Z,12Z)-octadeca-9,12-dienoyl]oxy-2-[(Z)-octadec-9-enoyl]oxypropyl] (Z)-octadec-9-enoate
SMILES (Canonical) CCCCCCCCC=CCCCCCCCC(=O)OCC(COC(=O)CCCCCCCC=CCC=CCCCCC)OC(=O)CCCCCCCC=CCCCCCCCC
SMILES (Isomeric) CCCCCCCC/C=C\CCCCCCCC(=O)OCC(COC(=O)CCCCCCC/C=C\C/C=C\CCCCC)OC(=O)CCCCCCC/C=C\CCCCCCCC
InChI InChI=1S/C57H102O6/c1-4-7-10-13-16-19-22-25-28-31-34-37-40-43-46-49-55(58)61-52-54(63-57(60)51-48-45-42-39-36-33-30-27-24-21-18-15-12-9-6-3)53-62-56(59)50-47-44-41-38-35-32-29-26-23-20-17-14-11-8-5-2/h16,19,25-30,54H,4-15,17-18,20-24,31-53H2,1-3H3/b19-16-,28-25-,29-26-,30-27-
InChI Key JTMWOTXEVWLTTO-KTKRTRQNSA-N
Popularity 7 references in papers

Physical and Chemical Properties

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Molecular Formula C57H102O6
Molecular Weight 883.40 g/mol
Exact Mass 882.76764097 g/mol
Topological Polar Surface Area (TPSA) 78.90 Ų
XlogP 21.70
Atomic LogP (AlogP) 17.87
H-Bond Acceptor 6
H-Bond Donor 0
Rotatable Bonds 49

Synonyms

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1-Linoleo-2,3-diolein
2,3-Dioleo-1-linolein
3-Linoleo-1,2-diolein
Linolein, 2,3-dioleo-1-
1,2-Dioleoyl-3-linoleoyl-rac-glycerol
Olein, 3-linoleo-1,2-di-
2190-20-7
9790LE118Y
UNII-9790LE118Y
9,12-Octadecadienoic acid (9Z,12Z)-, 2,3-bis(((9Z)-1-oxo-9-octadecen-1-yl)oxy)propyl ester
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 1,2-Dioleoyl-3-linolein

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9698 96.98%
Caco-2 - 0.8129 81.29%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.7145 71.45%
OATP2B1 inhibitior - 0.7156 71.56%
OATP1B1 inhibitior - 0.3596 35.96%
OATP1B3 inhibitior + 0.9462 94.62%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.9089 90.89%
P-glycoprotein inhibitior + 0.7440 74.40%
P-glycoprotein substrate - 0.8567 85.67%
CYP3A4 substrate - 0.5118 51.18%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8696 86.96%
CYP3A4 inhibition - 0.8012 80.12%
CYP2C9 inhibition - 0.8813 88.13%
CYP2C19 inhibition - 0.7771 77.71%
CYP2D6 inhibition - 0.9261 92.61%
CYP1A2 inhibition - 0.8125 81.25%
CYP2C8 inhibition - 0.7657 76.57%
CYP inhibitory promiscuity - 0.8092 80.92%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6523 65.23%
Carcinogenicity (trinary) Non-required 0.5477 54.77%
Eye corrosion - 0.7284 72.84%
Eye irritation - 0.8490 84.90%
Skin irritation - 0.6892 68.92%
Skin corrosion - 0.9815 98.15%
Ames mutagenesis - 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4447 44.47%
Micronuclear - 0.9400 94.00%
Hepatotoxicity - 0.5217 52.17%
skin sensitisation - 0.9321 93.21%
Respiratory toxicity - 0.8556 85.56%
Reproductive toxicity - 1.0000 100.00%
Mitochondrial toxicity - 0.9625 96.25%
Nephrotoxicity - 0.6377 63.77%
Acute Oral Toxicity (c) IV 0.6768 67.68%
Estrogen receptor binding + 0.8237 82.37%
Androgen receptor binding - 0.7683 76.83%
Thyroid receptor binding - 0.6204 62.04%
Glucocorticoid receptor binding - 0.5609 56.09%
Aromatase binding - 0.5538 55.38%
PPAR gamma + 0.5776 57.76%
Honey bee toxicity - 0.9609 96.09%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity + 0.8478 84.78%
Fish aquatic toxicity + 0.9716 97.16%

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 98.69% 99.17%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 96.03% 85.94%
CHEMBL2581 P07339 Cathepsin D 95.76% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.91% 96.09%
CHEMBL230 P35354 Cyclooxygenase-2 92.64% 89.63%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 91.68% 92.08%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 88.99% 97.29%
CHEMBL5255 O00206 Toll-like receptor 4 87.17% 92.50%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 85.60% 96.95%
CHEMBL1781 P11387 DNA topoisomerase I 84.85% 97.00%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 84.85% 95.17%
CHEMBL299 P17252 Protein kinase C alpha 84.75% 98.03%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 84.57% 92.86%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.02% 96.00%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 83.82% 97.21%
CHEMBL221 P23219 Cyclooxygenase-1 83.65% 90.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.27% 86.33%
CHEMBL3359 P21462 Formyl peptide receptor 1 81.91% 93.56%
CHEMBL4227 P25090 Lipoxin A4 receptor 81.71% 100.00%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 81.65% 100.00%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 81.41% 94.33%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 81.37% 91.81%

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.
Celastrus paniculatus

Cross-Links

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PubChem 9544252
LOTUS LTS0163084
wikiData Q104253541