Dimethyl suberate

Details

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Internal ID 6dce06af-94dc-4110-8eab-cab75f46dd00
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acid esters > Fatty acid methyl esters
IUPAC Name dimethyl octanedioate
SMILES (Canonical) COC(=O)CCCCCCC(=O)OC
SMILES (Isomeric) COC(=O)CCCCCCC(=O)OC
InChI InChI=1S/C10H18O4/c1-13-9(11)7-5-3-4-6-8-10(12)14-2/h3-8H2,1-2H3
InChI Key LNLCRJXCNQABMV-UHFFFAOYSA-N
Popularity 37 references in papers

Physical and Chemical Properties

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Molecular Formula C10H18O4
Molecular Weight 202.25 g/mol
Exact Mass 202.12050905 g/mol
Topological Polar Surface Area (TPSA) 52.60 Ų
XlogP 1.90
Atomic LogP (AlogP) 1.67
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 7

Synonyms

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Dimethyl octanedioate
1732-09-8
Octanedioic acid, dimethyl ester
Suberic acid, dimethyl ester
SUBERIC ACID DIMETHYL ESTER
Octanedioic acid dimethyl ester
Octanedioic acid dimethyl
Octanedioic acid, 1,8-dimethyl ester
EINECS 217-059-5
Hexane-1,6-dicarboxylic acid 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 suberate

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 + 0.9426 94.26%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.8550 85.50%
OATP2B1 inhibitior - 0.8468 84.68%
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 - 0.9050 90.50%
P-glycoprotein inhibitior - 0.9647 96.47%
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 + 0.9761 97.61%
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 - 0.4262 42.62%
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 - 0.9262 92.62%
Androgen receptor binding - 0.9234 92.34%
Thyroid receptor binding - 0.7776 77.76%
Glucocorticoid receptor binding - 0.7374 73.74%
Aromatase binding - 0.8323 83.23%
PPAR gamma - 0.8400 84.00%
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.
Astragalus trimestris
Pueraria montana var. lobata
Trollius chinensis

Cross-Links

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PubChem 15611
NPASS NPC198847
LOTUS LTS0138723
wikiData Q27155283