Dimethyl sebacate

Details

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Internal ID f50919d8-df18-482f-a228-9e3136646b2a
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acid esters > Fatty acid methyl esters
IUPAC Name dimethyl decanedioate
SMILES (Canonical) COC(=O)CCCCCCCCC(=O)OC
SMILES (Isomeric) COC(=O)CCCCCCCCC(=O)OC
InChI InChI=1S/C12H22O4/c1-15-11(13)9-7-5-3-4-6-8-10-12(14)16-2/h3-10H2,1-2H3
InChI Key ALOUNLDAKADEEB-UHFFFAOYSA-N
Popularity 91 references in papers

Physical and Chemical Properties

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Molecular Formula C12H22O4
Molecular Weight 230.30 g/mol
Exact Mass 230.15180918 g/mol
Topological Polar Surface Area (TPSA) 52.60 Ų
XlogP 3.00
Atomic LogP (AlogP) 2.45
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 9

Synonyms

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Dimethyl decanedioate
106-79-6
Sebacic acid dimethyl ester
Decanedioic acid, dimethyl ester
Methyl sebacate
Sebacic acid, dimethyl ester
Dimethyl octane-1,8-dicarboxylate
Dimethyldecanedioate
dimethyl decane-1,10-dioate
Decanedioic acid, 1,10-dimethyl 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 Dimethyl sebacate

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 + 0.8508 85.08%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.8550 85.50%
OATP2B1 inhibitior - 0.8476 84.76%
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 - 0.7291 72.91%
P-glycoprotein inhibitior - 0.8984 89.84%
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 + 0.8536 85.36%
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 - 0.4570 45.70%
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 - 0.9008 90.08%
Androgen receptor binding - 0.9154 91.54%
Thyroid receptor binding - 0.6820 68.20%
Glucocorticoid receptor binding - 0.7854 78.54%
Aromatase binding - 0.7378 73.78%
PPAR gamma - 0.8545 85.45%
Honey bee toxicity - 0.9715 97.15%
Biodegradation + 0.7000 70.00%
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!
To see more specific details click the taxa you are interested in.
Angelica sinensis
Astragalus trimestris
Glycyrrhiza uralensis
Sextonia rubra
Typha angustifolia
Typha orientalis

Cross-Links

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PubChem 7829
NPASS NPC219536
LOTUS LTS0071770
wikiData Q27278920