Dimethyl tetradecanedioate

Details

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Internal ID de671d3a-e621-4a47-92db-c93ef1d7e25d
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acid esters > Fatty acid methyl esters
IUPAC Name dimethyl tetradecanedioate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C16H30O4/c1-19-15(17)13-11-9-7-5-3-4-6-8-10-12-14-16(18)20-2/h3-14H2,1-2H3
InChI Key ZDJFDFNNEAPGOP-UHFFFAOYSA-N
Popularity 7 references in papers

Physical and Chemical Properties

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Molecular Formula C16H30O4
Molecular Weight 286.41 g/mol
Exact Mass 286.21440943 g/mol
Topological Polar Surface Area (TPSA) 52.60 Ų
XlogP 5.20
Atomic LogP (AlogP) 4.01
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 13

Synonyms

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5024-21-5
Tetradecanedioic acid, dimethyl ester
1,14-Dodecanedicarboxylic acid dimethyl ester
Tetradecanedioic Acid Dimethyl Ester
Tetradecanedioic acid, 1,14-dimethyl ester
7GWB0779K1
NSC-9505
NSC 9505
EINECS 225-711-5
SCHEMBL494114
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Dimethyl tetradecanedioate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9601 96.01%
Caco-2 + 0.8238 82.38%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.8550 85.50%
OATP2B1 inhibitior - 0.8493 84.93%
OATP1B1 inhibitior + 0.9642 96.42%
OATP1B3 inhibitior + 0.9520 95.20%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.5000 50.00%
P-glycoprotein inhibitior - 0.7830 78.30%
P-glycoprotein substrate - 0.9640 96.40%
CYP3A4 substrate - 0.6819 68.19%
CYP2C9 substrate - 0.8090 80.90%
CYP2D6 substrate - 0.8365 83.65%
CYP3A4 inhibition - 0.9731 97.31%
CYP2C9 inhibition - 0.9286 92.86%
CYP2C19 inhibition - 0.9626 96.26%
CYP2D6 inhibition - 0.9566 95.66%
CYP1A2 inhibition - 0.9053 90.53%
CYP2C8 inhibition - 0.9826 98.26%
CYP inhibitory promiscuity - 0.9526 95.26%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6723 67.23%
Carcinogenicity (trinary) Non-required 0.8272 82.72%
Eye corrosion + 0.8500 85.00%
Eye irritation + 0.9149 91.49%
Skin irritation - 0.9123 91.23%
Skin corrosion - 0.9965 99.65%
Ames mutagenesis - 0.9800 98.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6724 67.24%
Micronuclear - 0.9800 98.00%
Hepatotoxicity - 0.7032 70.32%
skin sensitisation - 0.9271 92.71%
Respiratory toxicity - 0.9444 94.44%
Reproductive toxicity - 0.9561 95.61%
Mitochondrial toxicity - 0.9000 90.00%
Nephrotoxicity + 0.5954 59.54%
Acute Oral Toxicity (c) III 0.8481 84.81%
Estrogen receptor binding - 0.8864 88.64%
Androgen receptor binding - 0.9070 90.70%
Thyroid receptor binding - 0.5523 55.23%
Glucocorticoid receptor binding - 0.7643 76.43%
Aromatase binding - 0.8348 83.48%
PPAR gamma - 0.5059 50.59%
Honey bee toxicity - 0.9715 97.15%
Biodegradation + 0.8000 80.00%
Crustacea aquatic toxicity + 0.5524 55.24%
Fish aquatic toxicity + 0.8999 89.99%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.36% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 93.52% 99.17%
CHEMBL4040 P28482 MAP kinase ERK2 90.38% 83.82%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.92% 91.11%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 84.77% 94.33%
CHEMBL2581 P07339 Cathepsin D 82.76% 98.95%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 81.93% 96.95%

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 78727
LOTUS LTS0008325
wikiData Q81990935