2,5-Diethyltetrahydrofuran

Details

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Internal ID 0dad1708-c917-4d02-8ac3-52ef608ece26
Taxonomy Organoheterocyclic compounds > Tetrahydrofurans
IUPAC Name 2,5-diethyloxolane
SMILES (Canonical) CCC1CCC(O1)CC
SMILES (Isomeric) CCC1CCC(O1)CC
InChI InChI=1S/C8H16O/c1-3-7-5-6-8(4-2)9-7/h7-8H,3-6H2,1-2H3
InChI Key YKWLEIXVUHRKEF-UHFFFAOYSA-N
Popularity 5 references in papers

Physical and Chemical Properties

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Molecular Formula C8H16O
Molecular Weight 128.21 g/mol
Exact Mass 128.120115130 g/mol
Topological Polar Surface Area (TPSA) 9.20 Ų
XlogP 2.50
Atomic LogP (AlogP) 2.35
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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2,5-diethyloxolane
41239-48-9
Furan, 2,5-diethyltetrahydro-
FEMA No. 3743
EINECS 255-274-6
UNII-4L4S1F79CT
2,5-Diethyltetrahydro-Furan
4L4S1F79CT
2,5-Diethyltetrahydrofurane
2,5-diethyl tetrahydrofuran
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 2,5-Diethyltetrahydrofuran

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9959 99.59%
Caco-2 + 0.8816 88.16%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Lysosomes 0.4155 41.55%
OATP2B1 inhibitior - 0.8409 84.09%
OATP1B1 inhibitior + 0.9667 96.67%
OATP1B3 inhibitior + 0.9507 95.07%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.9709 97.09%
P-glycoprotein inhibitior - 0.9823 98.23%
P-glycoprotein substrate - 0.9775 97.75%
CYP3A4 substrate - 0.7450 74.50%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7120 71.20%
CYP3A4 inhibition - 0.9624 96.24%
CYP2C9 inhibition - 0.8190 81.90%
CYP2C19 inhibition - 0.7529 75.29%
CYP2D6 inhibition - 0.9175 91.75%
CYP1A2 inhibition - 0.5775 57.75%
CYP2C8 inhibition - 0.9700 97.00%
CYP inhibitory promiscuity - 0.7124 71.24%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8200 82.00%
Carcinogenicity (trinary) Non-required 0.5638 56.38%
Eye corrosion + 0.8083 80.83%
Eye irritation + 0.9745 97.45%
Skin irritation + 0.6462 64.62%
Skin corrosion - 0.9332 93.32%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6262 62.62%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.7176 71.76%
skin sensitisation + 0.6260 62.60%
Respiratory toxicity - 0.7556 75.56%
Reproductive toxicity - 0.6844 68.44%
Mitochondrial toxicity - 0.9125 91.25%
Nephrotoxicity + 0.5438 54.38%
Acute Oral Toxicity (c) III 0.8592 85.92%
Estrogen receptor binding - 0.8901 89.01%
Androgen receptor binding - 0.8835 88.35%
Thyroid receptor binding - 0.8275 82.75%
Glucocorticoid receptor binding - 0.9326 93.26%
Aromatase binding - 0.8448 84.48%
PPAR gamma - 0.8341 83.41%
Honey bee toxicity - 0.9820 98.20%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.7100 71.00%
Fish aquatic toxicity - 0.4388 43.88%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.71% 97.25%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.11% 97.09%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.29% 96.09%
CHEMBL226 P30542 Adenosine A1 receptor 85.23% 95.93%

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.
Mentha arvensis
Mentha canadensis

Cross-Links

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PubChem 62913
NPASS NPC57535