Ethylene glycol dibutyl ether

Details

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Internal ID 3fc14a26-563e-485a-9e15-99a3bdbce514
Taxonomy Organic oxygen compounds > Organooxygen compounds > Ethers > Dialkyl ethers
IUPAC Name 1-(2-butoxyethoxy)butane
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H22O2/c1-3-5-7-11-9-10-12-8-6-4-2/h3-10H2,1-2H3
InChI Key GDXHBFHOEYVPED-UHFFFAOYSA-N
Popularity 40 references in papers

Physical and Chemical Properties

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Molecular Formula C10H22O2
Molecular Weight 174.28 g/mol
Exact Mass 174.161979940 g/mol
Topological Polar Surface Area (TPSA) 18.50 Ų
XlogP 2.50
Atomic LogP (AlogP) 2.62
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 9

Synonyms

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Ethylene glycol di-n-butyl ether
1,2-DIBUTOXYETHANE
Glycol dibutyl ether
HSDB 2827
Ethyl glycol dibutyl ether
EINECS 203-976-8
UNII-1HZO49D869
BRN 1738358
AI3-19429
1HZO49D869
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Ethylene glycol dibutyl ether

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9936 99.36%
Caco-2 + 0.9544 95.44%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Mitochondria 0.4641 46.41%
OATP2B1 inhibitior - 0.8476 84.76%
OATP1B1 inhibitior + 0.9122 91.22%
OATP1B3 inhibitior + 0.9349 93.49%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.7983 79.83%
P-glycoprotein inhibitior - 0.9626 96.26%
P-glycoprotein substrate - 0.9553 95.53%
CYP3A4 substrate - 0.6505 65.05%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7019 70.19%
CYP3A4 inhibition - 0.9691 96.91%
CYP2C9 inhibition - 0.9032 90.32%
CYP2C19 inhibition - 0.8825 88.25%
CYP2D6 inhibition - 0.9393 93.93%
CYP1A2 inhibition - 0.7408 74.08%
CYP2C8 inhibition - 0.9384 93.84%
CYP inhibitory promiscuity - 0.9157 91.57%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6300 63.00%
Carcinogenicity (trinary) Non-required 0.6183 61.83%
Eye corrosion + 0.9743 97.43%
Eye irritation + 0.9950 99.50%
Skin irritation - 0.7301 73.01%
Skin corrosion - 0.9858 98.58%
Ames mutagenesis - 0.9854 98.54%
Human Ether-a-go-go-Related Gene inhibition - 0.6472 64.72%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.5250 52.50%
skin sensitisation + 0.6754 67.54%
Respiratory toxicity - 0.9778 97.78%
Reproductive toxicity - 0.7444 74.44%
Mitochondrial toxicity - 1.0000 100.00%
Nephrotoxicity + 0.7260 72.60%
Acute Oral Toxicity (c) III 0.8136 81.36%
Estrogen receptor binding - 0.8891 88.91%
Androgen receptor binding - 0.9073 90.73%
Thyroid receptor binding - 0.6813 68.13%
Glucocorticoid receptor binding - 0.8602 86.02%
Aromatase binding - 0.8412 84.12%
PPAR gamma - 0.8840 88.40%
Honey bee toxicity - 0.9867 98.67%
Biodegradation + 0.7750 77.50%
Crustacea aquatic toxicity - 0.7252 72.52%
Fish aquatic toxicity + 0.6528 65.28%

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
CHEMBL1907 P15144 Aminopeptidase N 92.81% 93.31%
CHEMBL2581 P07339 Cathepsin D 89.65% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.72% 96.09%
CHEMBL240 Q12809 HERG 86.96% 89.76%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.39% 99.17%
CHEMBL253 P34972 Cannabinoid CB2 receptor 83.39% 97.25%
CHEMBL2885 P07451 Carbonic anhydrase III 82.86% 87.45%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 81.83% 97.29%
CHEMBL1075162 Q13304 Uracil nucleotide/cysteinyl leukotriene receptor 80.42% 80.33%
CHEMBL2664 P23526 Adenosylhomocysteinase 80.29% 86.67%

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.
Liriope muscari
Ophiopogon japonicus

Cross-Links

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PubChem 8188
NPASS NPC288628