Trimyristin

Details

Top
Internal ID 3741c7d3-8371-4e1d-8cb8-6c760266d1fd
Taxonomy Lipids and lipid-like molecules > Glycerolipids > Triradylcglycerols > Triacylglycerols
IUPAC Name 2,3-di(tetradecanoyloxy)propyl tetradecanoate
SMILES (Canonical) CCCCCCCCCCCCCC(=O)OCC(COC(=O)CCCCCCCCCCCCC)OC(=O)CCCCCCCCCCCCC
SMILES (Isomeric) CCCCCCCCCCCCCC(=O)OCC(COC(=O)CCCCCCCCCCCCC)OC(=O)CCCCCCCCCCCCC
InChI InChI=1S/C45H86O6/c1-4-7-10-13-16-19-22-25-28-31-34-37-43(46)49-40-42(51-45(48)39-36-33-30-27-24-21-18-15-12-9-6-3)41-50-44(47)38-35-32-29-26-23-20-17-14-11-8-5-2/h42H,4-41H2,1-3H3
InChI Key DUXYWXYOBMKGIN-UHFFFAOYSA-N
Popularity 583 references in papers

Physical and Chemical Properties

Top
Molecular Formula C45H86O6
Molecular Weight 723.20 g/mol
Exact Mass 722.64244046 g/mol
Topological Polar Surface Area (TPSA) 78.90 Ų
XlogP 18.70
Atomic LogP (AlogP) 14.09
H-Bond Acceptor 6
H-Bond Donor 0
Rotatable Bonds 41

Synonyms

Top
555-45-3
Glyceryl trimyristate
Glycerol trimyristate
Myristin
propane-1,2,3-triyl tritetradecanoate
Dynasan 114
trimyristoylglycerol
Tritetradecanoin
Myristic acid triglyceride
Myristin, tri-
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

Top
2D Structure of Trimyristin

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9627 96.27%
Caco-2 - 0.7505 75.05%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability - 0.7000 70.00%
Subcellular localzation Mitochondria 0.8050 80.50%
OATP2B1 inhibitior - 0.8546 85.46%
OATP1B1 inhibitior + 0.8956 89.56%
OATP1B3 inhibitior + 0.9542 95.42%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior + 0.9339 93.39%
P-glycoprotein inhibitior + 0.6449 64.49%
P-glycoprotein substrate - 0.8825 88.25%
CYP3A4 substrate - 0.5864 58.64%
CYP2C9 substrate - 0.7977 79.77%
CYP2D6 substrate - 0.8679 86.79%
CYP3A4 inhibition - 0.8577 85.77%
CYP2C9 inhibition - 0.8761 87.61%
CYP2C19 inhibition - 0.7979 79.79%
CYP2D6 inhibition - 0.9263 92.63%
CYP1A2 inhibition - 0.8498 84.98%
CYP2C8 inhibition - 0.9156 91.56%
CYP inhibitory promiscuity - 0.8661 86.61%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6523 65.23%
Carcinogenicity (trinary) Non-required 0.5230 52.30%
Eye corrosion - 0.6076 60.76%
Eye irritation + 0.5665 56.65%
Skin irritation - 0.8935 89.35%
Skin corrosion - 0.9849 98.49%
Ames mutagenesis + 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6032 60.32%
Micronuclear - 0.9400 94.00%
Hepatotoxicity + 0.5857 58.57%
skin sensitisation - 0.9633 96.33%
Respiratory toxicity - 0.9333 93.33%
Reproductive toxicity - 0.9889 98.89%
Mitochondrial toxicity - 0.9500 95.00%
Nephrotoxicity + 0.5822 58.22%
Acute Oral Toxicity (c) IV 0.6365 63.65%
Estrogen receptor binding + 0.7368 73.68%
Androgen receptor binding - 0.9170 91.70%
Thyroid receptor binding - 0.6003 60.03%
Glucocorticoid receptor binding - 0.5710 57.10%
Aromatase binding - 0.6364 63.64%
PPAR gamma - 0.5210 52.10%
Honey bee toxicity - 0.9674 96.74%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity + 0.7604 76.04%
Fish aquatic toxicity + 0.9339 93.39%

Targets

Top

Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
CHEMBL1293235 P02545 Prelamin-A/C 17.8 nM
Potency
via Super-PRED

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL3060 Q9Y345 Glycine transporter 2 96.71% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.62% 96.09%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 94.65% 85.94%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 94.57% 95.17%
CHEMBL299 P17252 Protein kinase C alpha 94.19% 98.03%
CHEMBL2581 P07339 Cathepsin D 93.48% 98.95%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 92.05% 97.29%
CHEMBL5255 O00206 Toll-like receptor 4 88.72% 92.50%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 88.21% 92.08%
CHEMBL230 P35354 Cyclooxygenase-2 87.02% 89.63%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 86.50% 92.86%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 85.17% 96.95%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 82.33% 91.81%
CHEMBL340 P08684 Cytochrome P450 3A4 81.70% 91.19%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 81.65% 100.00%
CHEMBL4227 P25090 Lipoxin A4 receptor 80.37% 100.00%

Cross-Links

Top
PubChem 11148
NPASS NPC230828
LOTUS LTS0164572
wikiData Q304581