4-Ethyloxolan-2-one

Details

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Internal ID 7de13c13-b3b6-4727-b944-5feba21e7de4
Taxonomy Organoheterocyclic compounds > Lactones > Gamma butyrolactones
IUPAC Name 4-ethyloxolan-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C6H10O2/c1-2-5-3-6(7)8-4-5/h5H,2-4H2,1H3
InChI Key MDQZVJSUBKPTHG-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C6H10O2
Molecular Weight 114.14 g/mol
Exact Mass 114.068079557 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 1.00
Atomic LogP (AlogP) 0.96
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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16496-51-8
4-ethyldihydrofuran-2(3H)-one
2(3H)-Furanone, 4-ethyldihydro-
Aethyl-butyrolacton
Aethyl-butyrolacton [German]
BRN 0107277
Dihydro-4-ethyl-2(3H)-furanone
2(3H)-FURANONE, DIHYDRO-4-ETHYL-
4-Ethylbutan-4-olide
5-17-09-00042 (Beilstein Handbook Reference)
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 4-Ethyloxolan-2-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.6666 66.66%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.5475 54.75%
OATP2B1 inhibitior - 0.8471 84.71%
OATP1B1 inhibitior + 0.9489 94.89%
OATP1B3 inhibitior + 0.9512 95.12%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.9014 90.14%
P-glycoprotein inhibitior - 0.9849 98.49%
P-glycoprotein substrate - 0.8949 89.49%
CYP3A4 substrate - 0.7144 71.44%
CYP2C9 substrate + 0.6168 61.68%
CYP2D6 substrate - 0.8637 86.37%
CYP3A4 inhibition - 0.9787 97.87%
CYP2C9 inhibition - 0.8383 83.83%
CYP2C19 inhibition - 0.7802 78.02%
CYP2D6 inhibition - 0.9443 94.43%
CYP1A2 inhibition - 0.6075 60.75%
CYP2C8 inhibition - 0.9846 98.46%
CYP inhibitory promiscuity - 0.9217 92.17%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8000 80.00%
Carcinogenicity (trinary) Non-required 0.6200 62.00%
Eye corrosion + 0.9040 90.40%
Eye irritation + 0.9928 99.28%
Skin irritation + 0.7068 70.68%
Skin corrosion - 0.7944 79.44%
Ames mutagenesis + 0.5716 57.16%
Human Ether-a-go-go-Related Gene inhibition - 0.8005 80.05%
Micronuclear - 0.8500 85.00%
Hepatotoxicity + 0.5634 56.34%
skin sensitisation - 0.7197 71.97%
Respiratory toxicity - 0.6667 66.67%
Reproductive toxicity - 0.8333 83.33%
Mitochondrial toxicity - 0.8625 86.25%
Nephrotoxicity + 0.5998 59.98%
Acute Oral Toxicity (c) III 0.9056 90.56%
Estrogen receptor binding - 0.9063 90.63%
Androgen receptor binding - 0.8595 85.95%
Thyroid receptor binding - 0.9325 93.25%
Glucocorticoid receptor binding - 0.9221 92.21%
Aromatase binding - 0.8315 83.15%
PPAR gamma - 0.8570 85.70%
Honey bee toxicity - 0.9101 91.01%
Biodegradation + 0.9000 90.00%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity + 0.7034 70.34%

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 93.38% 97.25%
CHEMBL2581 P07339 Cathepsin D 90.77% 98.95%
CHEMBL255 P29275 Adenosine A2b receptor 86.98% 98.59%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.38% 97.09%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.55% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.02% 95.56%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 27893
LOTUS LTS0086895
wikiData Q77309854