Isopropylethanediol

Details

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Internal ID 459ed1c6-236a-4d1d-9a21-87d9891457ef
Taxonomy Organic oxygen compounds > Organooxygen compounds > Ethers > Dialkyl ethers
IUPAC Name 2-propan-2-yloxyethanol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C5H12O2/c1-5(2)7-4-3-6/h5-6H,3-4H2,1-2H3
InChI Key HCGFUIQPSOCUHI-UHFFFAOYSA-N
Popularity 138 references in papers

Physical and Chemical Properties

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Molecular Formula C5H12O2
Molecular Weight 104.15 g/mol
Exact Mass 104.083729621 g/mol
Topological Polar Surface Area (TPSA) 29.50 Ų
XlogP 0.10
Atomic LogP (AlogP) 0.40
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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2-(1-Methylethoxy)ethanol
RefChem:792099
2-Isopropoxyethanol
109-59-1
Isopropyl oxitol
Dowanal EiPAT
Isopropyl cellosolve
Ethylene glycol isopropyl ether
ISOPROPOXYETHANOL
Ucar AC
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Isopropylethanediol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9829 98.29%
Caco-2 + 0.6305 63.05%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.5610 56.10%
OATP2B1 inhibitior - 0.8576 85.76%
OATP1B1 inhibitior + 0.9299 92.99%
OATP1B3 inhibitior + 0.9398 93.98%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.9607 96.07%
P-glycoprotein inhibitior - 0.9877 98.77%
P-glycoprotein substrate - 0.9698 96.98%
CYP3A4 substrate - 0.7336 73.36%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7761 77.61%
CYP3A4 inhibition - 0.9644 96.44%
CYP2C9 inhibition - 0.9428 94.28%
CYP2C19 inhibition - 0.8886 88.86%
CYP2D6 inhibition - 0.9447 94.47%
CYP1A2 inhibition - 0.8608 86.08%
CYP2C8 inhibition - 0.9897 98.97%
CYP inhibitory promiscuity - 0.9528 95.28%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.6300 63.00%
Carcinogenicity (trinary) Non-required 0.7742 77.42%
Eye corrosion + 0.8900 89.00%
Eye irritation + 0.9812 98.12%
Skin irritation + 0.8410 84.10%
Skin corrosion - 0.9252 92.52%
Ames mutagenesis - 0.7691 76.91%
Human Ether-a-go-go-Related Gene inhibition - 0.6949 69.49%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.8375 83.75%
skin sensitisation + 0.6755 67.55%
Respiratory toxicity - 0.8222 82.22%
Reproductive toxicity - 0.8000 80.00%
Mitochondrial toxicity - 0.9875 98.75%
Nephrotoxicity + 0.6556 65.56%
Acute Oral Toxicity (c) IV 0.6293 62.93%
Estrogen receptor binding - 0.8687 86.87%
Androgen receptor binding - 0.9293 92.93%
Thyroid receptor binding - 0.8174 81.74%
Glucocorticoid receptor binding - 0.8762 87.62%
Aromatase binding - 0.8974 89.74%
PPAR gamma - 0.8757 87.57%
Honey bee toxicity - 0.9328 93.28%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.9700 97.00%
Fish aquatic toxicity - 0.9786 97.86%

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
CHEMBL2885 P07451 Carbonic anhydrase III 94.00% 87.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.05% 96.09%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 82.77% 86.92%

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.
Cornus officinalis
Pterocarpus indicus

Cross-Links

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PubChem 7996
NPASS NPC272307