Neryl myristate

Details

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Internal ID 8fa98980-7d3a-4f4d-8169-70107e364d39
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acid esters > Wax esters > Wax monoesters
IUPAC Name [(2Z)-3,7-dimethylocta-2,6-dienyl] tetradecanoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C24H44O2/c1-5-6-7-8-9-10-11-12-13-14-15-19-24(25)26-21-20-23(4)18-16-17-22(2)3/h17,20H,5-16,18-19,21H2,1-4H3/b23-20-
InChI Key BVBISCLEXKZRHD-ATJXCDBQSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C24H44O2
Molecular Weight 364.60 g/mol
Exact Mass 364.334130642 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 9.70
Atomic LogP (AlogP) 7.92
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 17

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Neryl myristate

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 + 0.7042 70.42%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability - 0.7143 71.43%
Subcellular localzation Mitochondria 0.5488 54.88%
OATP2B1 inhibitior - 0.8530 85.30%
OATP1B1 inhibitior + 0.9182 91.82%
OATP1B3 inhibitior + 0.9094 90.94%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior + 0.9252 92.52%
P-glycoprotein inhibitior - 0.5924 59.24%
P-glycoprotein substrate - 0.9007 90.07%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 0.7977 79.77%
CYP2D6 substrate - 0.8708 87.08%
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 - 0.8620 86.20%
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 + 0.5920 59.20%
Skin irritation + 0.5000 50.00%
Skin corrosion - 0.9912 99.12%
Ames mutagenesis - 0.9228 92.28%
Human Ether-a-go-go-Related Gene inhibition + 0.6470 64.70%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.5375 53.75%
skin sensitisation - 0.6074 60.74%
Respiratory toxicity - 0.9111 91.11%
Reproductive toxicity - 1.0000 100.00%
Mitochondrial toxicity - 0.9875 98.75%
Nephrotoxicity + 0.6351 63.51%
Acute Oral Toxicity (c) IV 0.4928 49.28%
Estrogen receptor binding - 0.7399 73.99%
Androgen receptor binding - 0.8392 83.92%
Thyroid receptor binding - 0.5453 54.53%
Glucocorticoid receptor binding - 0.5856 58.56%
Aromatase binding - 0.5962 59.62%
PPAR gamma - 0.5366 53.66%
Honey bee toxicity - 0.9554 95.54%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity + 0.7918 79.18%
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
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 99.37% 92.08%
CHEMBL3060 Q9Y345 Glycine transporter 2 96.79% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.56% 96.09%
CHEMBL2581 P07339 Cathepsin D 92.26% 98.95%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 90.10% 85.94%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 89.91% 92.86%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 89.62% 97.29%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 85.00% 96.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.74% 94.45%
CHEMBL299 P17252 Protein kinase C alpha 84.68% 98.03%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 84.65% 91.24%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.61% 91.11%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 84.12% 100.00%
CHEMBL3401 O75469 Pregnane X receptor 83.91% 94.73%
CHEMBL230 P35354 Cyclooxygenase-2 83.29% 89.63%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 83.05% 94.33%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 82.56% 91.81%
CHEMBL340 P08684 Cytochrome P450 3A4 82.37% 91.19%
CHEMBL221 P23219 Cyclooxygenase-1 81.98% 90.17%
CHEMBL5255 O00206 Toll-like receptor 4 81.62% 92.50%
CHEMBL1293316 Q9HBX9 Relaxin receptor 1 80.22% 82.50%

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 129699789
LOTUS LTS0057976
wikiData Q104946438