Dimethyl adipate

Details

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Internal ID db47b14b-8fa0-47dc-8931-edee10ddf71a
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acid esters > Fatty acid methyl esters
IUPAC Name dimethyl hexanedioate
SMILES (Canonical) COC(=O)CCCCC(=O)OC
SMILES (Isomeric) COC(=O)CCCCC(=O)OC
InChI InChI=1S/C8H14O4/c1-11-7(9)5-3-4-6-8(10)12-2/h3-6H2,1-2H3
InChI Key UDSFAEKRVUSQDD-UHFFFAOYSA-N
Popularity 257 references in papers

Physical and Chemical Properties

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Molecular Formula C8H14O4
Molecular Weight 174.19 g/mol
Exact Mass 174.08920892 g/mol
Topological Polar Surface Area (TPSA) 52.60 Ų
XlogP 1.00
Atomic LogP (AlogP) 0.89
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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627-93-0
Dimethyl hexanedioate
HEXANEDIOIC ACID, DIMETHYL ESTER
Dimethyladipate
Adipic acid dimethyl ester
Adipic acid, dimethyl ester
1,6-Dimethylhexanedioate
DBE 6
Methyl adipate (VAN)
1,6-dimethyl hexanedioate
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 adipate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9502 95.02%
Caco-2 + 0.8775 87.75%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Mitochondria 0.8381 83.81%
OATP2B1 inhibitior - 0.8456 84.56%
OATP1B1 inhibitior + 0.9583 95.83%
OATP1B3 inhibitior + 0.9535 95.35%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9503 95.03%
P-glycoprotein inhibitior - 0.9783 97.83%
P-glycoprotein substrate - 0.9692 96.92%
CYP3A4 substrate - 0.7015 70.15%
CYP2C9 substrate - 0.8090 80.90%
CYP2D6 substrate - 0.8365 83.65%
CYP3A4 inhibition - 0.9679 96.79%
CYP2C9 inhibition - 0.9323 93.23%
CYP2C19 inhibition - 0.9564 95.64%
CYP2D6 inhibition - 0.9573 95.73%
CYP1A2 inhibition - 0.9037 90.37%
CYP2C8 inhibition - 0.9867 98.67%
CYP inhibitory promiscuity - 0.9435 94.35%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6423 64.23%
Carcinogenicity (trinary) Non-required 0.8032 80.32%
Eye corrosion + 0.8649 86.49%
Eye irritation + 0.9721 97.21%
Skin irritation - 0.8845 88.45%
Skin corrosion - 0.9925 99.25%
Ames mutagenesis - 1.0000 100.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4907 49.07%
Micronuclear - 0.9800 98.00%
Hepatotoxicity - 0.7065 70.65%
skin sensitisation - 0.9250 92.50%
Respiratory toxicity - 0.9556 95.56%
Reproductive toxicity - 0.9338 93.38%
Mitochondrial toxicity - 0.8875 88.75%
Nephrotoxicity + 0.5936 59.36%
Acute Oral Toxicity (c) III 0.8406 84.06%
Estrogen receptor binding - 0.9350 93.50%
Androgen receptor binding - 0.9315 93.15%
Thyroid receptor binding - 0.8772 87.72%
Glucocorticoid receptor binding - 0.8917 89.17%
Aromatase binding - 0.8633 86.33%
PPAR gamma - 0.9193 91.93%
Honey bee toxicity - 0.9699 96.99%
Biodegradation + 0.6750 67.50%
Crustacea aquatic toxicity - 0.6100 61.00%
Fish aquatic toxicity + 0.8001 80.01%

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 95.76% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.37% 99.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.08% 91.11%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 84.77% 94.33%
CHEMBL4040 P28482 MAP kinase ERK2 84.10% 83.82%
CHEMBL2581 P07339 Cathepsin D 82.65% 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
Biancaea sappan
Typha angustifolia
Typha orientalis

Cross-Links

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PubChem 12329
NPASS NPC57499
LOTUS LTS0214547
wikiData Q21994864