2-(2-(2-Methoxyethoxy)ethoxy)ethyl acetate

Details

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Internal ID 0b1e5b5b-764b-4875-b67e-ac9cbf783180
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Carboxylic acid derivatives > Carboxylic acid esters
IUPAC Name 2-[2-(2-methoxyethoxy)ethoxy]ethyl acetate
SMILES (Canonical) CC(=O)OCCOCCOCCOC
SMILES (Isomeric) CC(=O)OCCOCCOCCOC
InChI InChI=1S/C9H18O5/c1-9(10)14-8-7-13-6-5-12-4-3-11-2/h3-8H2,1-2H3
InChI Key SDHQGBWMLCBNSM-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C9H18O5
Molecular Weight 206.24 g/mol
Exact Mass 206.11542367 g/mol
Topological Polar Surface Area (TPSA) 54.00 Ų
XlogP -0.30
Atomic LogP (AlogP) 0.23
H-Bond Acceptor 5
H-Bond Donor 0
Rotatable Bonds 9

Synonyms

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Triethylene glycol monomethyl ether acetate
Methoxytriglycol acetate
2-[2-(2-methoxyethoxy)ethoxy]ethyl acetate
2-(2-(2-Methoxyethoxy)ethoxy)ethyl acetate
EINECS 222-777-7
VRV2GZK24O
NSC 403845
3,6,9-Trioxadecylester kyseliny octove
BRN 1775581
Ethanol, 2-(2-(2-methoxyethoxy)ethoxy)-, acetate
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 2-(2-(2-Methoxyethoxy)ethoxy)ethyl acetate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9466 94.66%
Caco-2 + 0.8028 80.28%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.7246 72.46%
OATP2B1 inhibitior - 0.8484 84.84%
OATP1B1 inhibitior + 0.9370 93.70%
OATP1B3 inhibitior + 0.9362 93.62%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.6563 65.63%
P-glycoprotein inhibitior - 0.9581 95.81%
P-glycoprotein substrate - 0.9650 96.50%
CYP3A4 substrate - 0.5462 54.62%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8800 88.00%
CYP3A4 inhibition - 0.9708 97.08%
CYP2C9 inhibition - 0.9472 94.72%
CYP2C19 inhibition - 0.9503 95.03%
CYP2D6 inhibition - 0.9558 95.58%
CYP1A2 inhibition - 0.9178 91.78%
CYP2C8 inhibition - 0.9769 97.69%
CYP inhibitory promiscuity - 0.9657 96.57%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6623 66.23%
Carcinogenicity (trinary) Non-required 0.6942 69.42%
Eye corrosion + 0.6852 68.52%
Eye irritation + 0.9375 93.75%
Skin irritation - 0.8529 85.29%
Skin corrosion - 0.9961 99.61%
Ames mutagenesis - 0.7280 72.80%
Human Ether-a-go-go-Related Gene inhibition - 0.7055 70.55%
Micronuclear - 0.9800 98.00%
Hepatotoxicity - 0.6216 62.16%
skin sensitisation - 0.8261 82.61%
Respiratory toxicity - 0.9889 98.89%
Reproductive toxicity - 0.5556 55.56%
Mitochondrial toxicity - 0.9875 98.75%
Nephrotoxicity + 0.7328 73.28%
Acute Oral Toxicity (c) IV 0.6487 64.87%
Estrogen receptor binding - 0.9119 91.19%
Androgen receptor binding - 0.9082 90.82%
Thyroid receptor binding - 0.7007 70.07%
Glucocorticoid receptor binding - 0.7211 72.11%
Aromatase binding - 0.8265 82.65%
PPAR gamma - 0.8416 84.16%
Honey bee toxicity - 0.8724 87.24%
Biodegradation + 0.8500 85.00%
Crustacea aquatic toxicity - 0.8600 86.00%
Fish aquatic toxicity + 0.7887 78.87%

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 96.30% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.29% 94.45%
CHEMBL253 P34972 Cannabinoid CB2 receptor 84.77% 97.25%
CHEMBL2885 P07451 Carbonic anhydrase III 82.75% 87.45%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 82.57% 94.33%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 81.62% 96.95%
CHEMBL3401 O75469 Pregnane X receptor 81.42% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.86% 99.17%

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.
Pterocarpus indicus

Cross-Links

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PubChem 19218
NPASS NPC307692