3,7,11,15-Tetramethylhexadec-2-enyl octadec-9-enoate

Details

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Internal ID fd46a8fa-8621-4cba-aa5d-2f53c48d7c59
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acid esters > Wax esters > Wax monoesters
IUPAC Name 3,7,11,15-tetramethylhexadec-2-enyl octadec-9-enoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C38H72O2/c1-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-31-38(39)40-33-32-37(6)30-24-29-36(5)28-23-27-35(4)26-22-25-34(2)3/h14-15,32,34-36H,7-13,16-31,33H2,1-6H3
InChI Key APQYNMFMLJBOIW-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C38H72O2
Molecular Weight 561.00 g/mol
Exact Mass 560.55323154 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 16.20
Atomic LogP (AlogP) 12.95
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 29

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3,7,11,15-Tetramethylhexadec-2-enyl octadec-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 + 0.9968 99.68%
Caco-2 - 0.7439 74.39%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.5488 54.88%
OATP2B1 inhibitior + 0.5709 57.09%
OATP1B1 inhibitior + 0.8700 87.00%
OATP1B3 inhibitior + 0.9094 90.94%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior + 0.9576 95.76%
P-glycoprotein inhibitior + 0.6458 64.58%
P-glycoprotein substrate - 0.6857 68.57%
CYP3A4 substrate + 0.5599 55.99%
CYP2C9 substrate - 0.8037 80.37%
CYP2D6 substrate - 0.8782 87.82%
CYP3A4 inhibition - 0.9267 92.67%
CYP2C9 inhibition - 0.9105 91.05%
CYP2C19 inhibition - 0.8736 87.36%
CYP2D6 inhibition - 0.9284 92.84%
CYP1A2 inhibition - 0.6823 68.23%
CYP2C8 inhibition - 0.7690 76.90%
CYP inhibitory promiscuity - 0.6530 65.30%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6200 62.00%
Carcinogenicity (trinary) Non-required 0.5336 53.36%
Eye corrosion + 0.7056 70.56%
Eye irritation - 0.7487 74.87%
Skin irritation + 0.5000 50.00%
Skin corrosion - 0.9912 99.12%
Ames mutagenesis - 0.9100 91.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4528 45.28%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.6467 64.67%
skin sensitisation - 0.6074 60.74%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity - 1.0000 100.00%
Mitochondrial toxicity - 0.9875 98.75%
Nephrotoxicity - 0.7658 76.58%
Acute Oral Toxicity (c) IV 0.4928 49.28%
Estrogen receptor binding + 0.6401 64.01%
Androgen receptor binding - 0.6908 69.08%
Thyroid receptor binding - 0.5413 54.13%
Glucocorticoid receptor binding + 0.5659 56.59%
Aromatase binding - 0.6139 61.39%
PPAR gamma - 0.5343 53.43%
Honey bee toxicity - 0.9441 94.41%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.8178 81.78%
Fish aquatic toxicity + 0.9876 98.76%

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 98.50% 99.17%
CHEMBL230 P35354 Cyclooxygenase-2 96.39% 89.63%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 96.26% 97.29%
CHEMBL2581 P07339 Cathepsin D 95.63% 98.95%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 94.80% 92.86%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 94.33% 92.08%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.16% 96.09%
CHEMBL3359 P21462 Formyl peptide receptor 1 91.54% 93.56%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 91.24% 85.94%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.16% 94.45%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 88.90% 96.47%
CHEMBL299 P17252 Protein kinase C alpha 88.66% 98.03%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 88.16% 100.00%
CHEMBL1907 P15144 Aminopeptidase N 87.78% 93.31%
CHEMBL4227 P25090 Lipoxin A4 receptor 87.21% 100.00%
CHEMBL3401 O75469 Pregnane X receptor 86.66% 94.73%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 85.74% 89.34%
CHEMBL221 P23219 Cyclooxygenase-1 84.83% 90.17%
CHEMBL2885 P07451 Carbonic anhydrase III 84.00% 87.45%
CHEMBL3267 P48736 PI3-kinase p110-gamma subunit 83.86% 95.71%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 83.54% 91.81%
CHEMBL340 P08684 Cytochrome P450 3A4 83.04% 91.19%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.85% 91.11%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 82.65% 100.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.58% 96.00%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 82.02% 94.33%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 81.64% 90.71%
CHEMBL5255 O00206 Toll-like receptor 4 81.19% 92.50%
CHEMBL1293316 Q9HBX9 Relaxin receptor 1 80.87% 82.50%
CHEMBL5163 Q9NY46 Sodium channel protein type III alpha subunit 80.81% 96.90%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.70% 96.95%
CHEMBL1781 P11387 DNA topoisomerase I 80.50% 97.00%

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.
Goniophlebium mengtzeense

Cross-Links

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PubChem 53655585
LOTUS LTS0216358
wikiData Q104916492