Ether, isobutyl methyl

Details

Top
Internal ID 77ab2cce-fe59-4f01-bc05-8a834455572a
Taxonomy Organic oxygen compounds > Organooxygen compounds > Ethers > Dialkyl ethers
IUPAC Name 1-methoxy-2-methylpropane
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C5H12O/c1-5(2)4-6-3/h5H,4H2,1-3H3
InChI Key ZYVYEJXMYBUCMN-UHFFFAOYSA-N
Popularity 74 references in papers

Physical and Chemical Properties

Top
Molecular Formula C5H12O
Molecular Weight 88.15 g/mol
Exact Mass 88.088815002 g/mol
Topological Polar Surface Area (TPSA) 9.20 Ų
XlogP 1.40
Atomic LogP (AlogP) 1.29
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

Top
Ether, isobutyl methyl
METHYL ISOBUTYL ETHER
Methyl isobutyl oxide
625-44-5
BRN 1730971
DTXSID70211540
1Methoxy2methylpropane
Propane, 1methoxy2methyl
RefChem:592689
DTXCID00134031
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

Top
2D Structure of Ether, isobutyl methyl

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9886 98.86%
Caco-2 + 0.5081 50.81%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.7571 75.71%
Subcellular localzation Mitochondria 0.5369 53.69%
OATP2B1 inhibitior - 0.8661 86.61%
OATP1B1 inhibitior + 0.9640 96.40%
OATP1B3 inhibitior + 0.9511 95.11%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9418 94.18%
P-glycoprotein inhibitior - 0.9812 98.12%
P-glycoprotein substrate - 0.9652 96.52%
CYP3A4 substrate - 0.7262 72.62%
CYP2C9 substrate - 0.7613 76.13%
CYP2D6 substrate - 0.7547 75.47%
CYP3A4 inhibition - 0.9890 98.90%
CYP2C9 inhibition - 0.9611 96.11%
CYP2C19 inhibition - 0.9398 93.98%
CYP2D6 inhibition - 0.9494 94.94%
CYP1A2 inhibition - 0.8748 87.48%
CYP2C8 inhibition - 0.9924 99.24%
CYP inhibitory promiscuity - 0.9390 93.90%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5083 50.83%
Carcinogenicity (trinary) Non-required 0.4720 47.20%
Eye corrosion + 0.9523 95.23%
Eye irritation + 0.9970 99.70%
Skin irritation + 0.5692 56.92%
Skin corrosion - 0.9808 98.08%
Ames mutagenesis - 0.7308 73.08%
Human Ether-a-go-go-Related Gene inhibition - 0.7930 79.30%
Micronuclear - 0.9700 97.00%
Hepatotoxicity - 0.5091 50.91%
skin sensitisation + 0.6570 65.70%
Respiratory toxicity - 0.7000 70.00%
Reproductive toxicity - 0.7145 71.45%
Mitochondrial toxicity - 0.9375 93.75%
Nephrotoxicity + 0.6063 60.63%
Acute Oral Toxicity (c) III 0.6590 65.90%
Estrogen receptor binding - 0.9071 90.71%
Androgen receptor binding - 0.8444 84.44%
Thyroid receptor binding - 0.9053 90.53%
Glucocorticoid receptor binding - 0.9217 92.17%
Aromatase binding - 0.8152 81.52%
PPAR gamma - 0.9292 92.92%
Honey bee toxicity - 0.8170 81.70%
Biodegradation + 0.6500 65.00%
Crustacea aquatic toxicity - 0.7000 70.00%
Fish aquatic toxicity - 0.6995 69.95%

Targets

Top

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 92.33% 96.09%
CHEMBL2885 P07451 Carbonic anhydrase III 91.73% 87.45%
CHEMBL2581 P07339 Cathepsin D 86.08% 98.95%
CHEMBL1907 P15144 Aminopeptidase N 84.37% 93.31%

Plants that contains it

Top
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.
Glycyrrhiza glabra

Cross-Links

Top
PubChem 12250
LOTUS LTS0056664
wikiData Q29414987