Diethylene glycol monobenzoate

Details

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Internal ID 103c27c7-4da5-4acc-a989-fe33ba674091
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzoic acids and derivatives > Benzoic acid esters
IUPAC Name 2-(2-hydroxyethoxy)ethyl benzoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C11H14O4/c12-6-7-14-8-9-15-11(13)10-4-2-1-3-5-10/h1-5,12H,6-9H2
InChI Key DNUPYEDSAQDUSO-UHFFFAOYSA-N
Popularity 10 references in papers

Physical and Chemical Properties

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Molecular Formula C11H14O4
Molecular Weight 210.23 g/mol
Exact Mass 210.08920892 g/mol
Topological Polar Surface Area (TPSA) 55.80 Ų
XlogP 1.20
Atomic LogP (AlogP) 0.85
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 6

Synonyms

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20587-61-5
Diethylene glycol monobenzoate
Ethanol, 2-[2-(benzoyloxy)ethoxy]-
Diethylene glycol benzoate
Ethanol, 2-(2-(benzoyloxy)ethoxy)-
Ethanol, 2,2'-oxybis-, monobenzoate
EINECS 243-895-5
NSC 71576
U8NT2B98P1
AI3-13034
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Diethylene glycol monobenzoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9037 90.37%
Caco-2 + 0.8727 87.27%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.8417 84.17%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8809 88.09%
OATP1B3 inhibitior + 0.9202 92.02%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.9389 93.89%
P-glycoprotein inhibitior - 0.9796 97.96%
P-glycoprotein substrate - 0.9701 97.01%
CYP3A4 substrate - 0.6492 64.92%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8198 81.98%
CYP3A4 inhibition - 0.9385 93.85%
CYP2C9 inhibition - 0.8928 89.28%
CYP2C19 inhibition - 0.8732 87.32%
CYP2D6 inhibition - 0.9529 95.29%
CYP1A2 inhibition - 0.9272 92.72%
CYP2C8 inhibition - 0.7161 71.61%
CYP inhibitory promiscuity - 0.9522 95.22%
UGT catelyzed - 0.7000 70.00%
Carcinogenicity (binary) - 0.8700 87.00%
Carcinogenicity (trinary) Non-required 0.7073 70.73%
Eye corrosion - 0.7439 74.39%
Eye irritation + 0.9682 96.82%
Skin irritation - 0.6450 64.50%
Skin corrosion - 0.9883 98.83%
Ames mutagenesis - 0.8700 87.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6452 64.52%
Micronuclear - 0.9600 96.00%
Hepatotoxicity - 0.5500 55.00%
skin sensitisation - 0.6540 65.40%
Respiratory toxicity - 0.7333 73.33%
Reproductive toxicity - 0.7679 76.79%
Mitochondrial toxicity - 0.6125 61.25%
Nephrotoxicity + 0.4856 48.56%
Acute Oral Toxicity (c) III 0.7094 70.94%
Estrogen receptor binding + 0.5457 54.57%
Androgen receptor binding - 0.6786 67.86%
Thyroid receptor binding - 0.6983 69.83%
Glucocorticoid receptor binding - 0.8218 82.18%
Aromatase binding - 0.5582 55.82%
PPAR gamma - 0.5099 50.99%
Honey bee toxicity - 0.9627 96.27%
Biodegradation + 0.7000 70.00%
Crustacea aquatic toxicity - 0.8200 82.00%
Fish aquatic toxicity + 0.6611 66.11%

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
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 92.41% 94.62%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.06% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.46% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.85% 99.17%
CHEMBL2581 P07339 Cathepsin D 84.37% 98.95%
CHEMBL4267 P37173 TGF-beta receptor type II 82.00% 88.18%
CHEMBL3401 O75469 Pregnane X receptor 81.20% 94.73%

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.
Santalum album

Cross-Links

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PubChem 88603
NPASS NPC252053
LOTUS LTS0181745
wikiData Q27290899