Ethyl isopropyl ether

Details

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Internal ID c760113f-7859-4365-b3f0-d98d96119d6d
Taxonomy Organic oxygen compounds > Organooxygen compounds > Ethers > Dialkyl ethers
IUPAC Name 2-ethoxypropane
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C5H12O/c1-4-6-5(2)3/h5H,4H2,1-3H3
InChI Key XSJVWZAETSBXKU-UHFFFAOYSA-N
Popularity 199 references in papers

Physical and Chemical Properties

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Molecular Formula C5H12O
Molecular Weight 88.15 g/mol
Exact Mass 88.088815002 g/mol
Topological Polar Surface Area (TPSA) 9.20 Ų
XlogP 0.90
Atomic LogP (AlogP) 1.43
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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2-Ethoxypropane
625-54-7
Propane, 2-ethoxy-
Ether, ethyl isopropyl
MFCD00043532
Isopropyl ethyl ether
EINECS 210-900-7
BRN 1730945
Methylather
68FC4UEX7L
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Ethyl isopropyl ether

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9966 99.66%
Caco-2 + 0.5996 59.96%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.8429 84.29%
Subcellular localzation Mitochondria 0.6144 61.44%
OATP2B1 inhibitior - 0.8652 86.52%
OATP1B1 inhibitior + 0.9565 95.65%
OATP1B3 inhibitior + 0.9559 95.59%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9453 94.53%
P-glycoprotein inhibitior - 0.9854 98.54%
P-glycoprotein substrate - 0.9787 97.87%
CYP3A4 substrate - 0.7533 75.33%
CYP2C9 substrate - 0.8060 80.60%
CYP2D6 substrate - 0.7521 75.21%
CYP3A4 inhibition - 0.9856 98.56%
CYP2C9 inhibition - 0.9281 92.81%
CYP2C19 inhibition - 0.9061 90.61%
CYP2D6 inhibition - 0.9379 93.79%
CYP1A2 inhibition - 0.6789 67.89%
CYP2C8 inhibition - 0.9896 98.96%
CYP inhibitory promiscuity - 0.7579 75.79%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5100 51.00%
Carcinogenicity (trinary) Non-required 0.5408 54.08%
Eye corrosion + 0.8426 84.26%
Eye irritation + 0.9950 99.50%
Skin irritation + 0.7947 79.47%
Skin corrosion - 0.9843 98.43%
Ames mutagenesis - 0.7744 77.44%
Human Ether-a-go-go-Related Gene inhibition - 0.8039 80.39%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.5976 59.76%
skin sensitisation + 0.5275 52.75%
Respiratory toxicity - 0.7667 76.67%
Reproductive toxicity - 0.9222 92.22%
Mitochondrial toxicity - 0.9000 90.00%
Nephrotoxicity + 0.6786 67.86%
Acute Oral Toxicity (c) III 0.6247 62.47%
Estrogen receptor binding - 0.9077 90.77%
Androgen receptor binding - 0.9254 92.54%
Thyroid receptor binding - 0.8589 85.89%
Glucocorticoid receptor binding - 0.9361 93.61%
Aromatase binding - 0.8845 88.45%
PPAR gamma - 0.8678 86.78%
Honey bee toxicity - 0.8329 83.29%
Biodegradation + 0.6000 60.00%
Crustacea aquatic toxicity - 0.7300 73.00%
Fish aquatic toxicity - 0.5103 51.03%

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 90.02% 96.09%
CHEMBL2885 P07451 Carbonic anhydrase III 82.82% 87.45%

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.
Litchi chinensis
Pterocarpus indicus

Cross-Links

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PubChem 12256
NPASS NPC62801