2(3H)-Furanone, 4-ethyldihydro-3-hydroxy-4-methyl-

Details

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Internal ID 8f1ccfe7-4656-42ad-8cde-65123e70bb0f
Taxonomy Organoheterocyclic compounds > Lactones > Gamma butyrolactones
IUPAC Name 4-ethyl-3-hydroxy-4-methyloxolan-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C7H12O3/c1-3-7(2)4-10-6(9)5(7)8/h5,8H,3-4H2,1-2H3
InChI Key UDNSVMRLHHBYOK-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C7H12O3
Molecular Weight 144.17 g/mol
Exact Mass 144.078644241 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 0.80
Atomic LogP (AlogP) 0.32
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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2(3H)-Furanone, 4-ethyldihydro-3-hydroxy-4-methyl-
57606-04-9

2D Structure

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2D Structure of 2(3H)-Furanone, 4-ethyldihydro-3-hydroxy-4-methyl-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9753 97.53%
Caco-2 + 0.6984 69.84%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Mitochondria 0.7380 73.80%
OATP2B1 inhibitior - 0.8325 83.25%
OATP1B1 inhibitior + 0.9526 95.26%
OATP1B3 inhibitior + 0.9467 94.67%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.8892 88.92%
P-glycoprotein inhibitior - 0.9814 98.14%
P-glycoprotein substrate - 0.8988 89.88%
CYP3A4 substrate - 0.6247 62.47%
CYP2C9 substrate - 0.8129 81.29%
CYP2D6 substrate - 0.8536 85.36%
CYP3A4 inhibition - 0.8276 82.76%
CYP2C9 inhibition - 0.7761 77.61%
CYP2C19 inhibition - 0.8417 84.17%
CYP2D6 inhibition - 0.9412 94.12%
CYP1A2 inhibition - 0.7987 79.87%
CYP2C8 inhibition - 0.9882 98.82%
CYP inhibitory promiscuity - 0.8629 86.29%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.5856 58.56%
Eye corrosion - 0.9095 90.95%
Eye irritation + 0.8670 86.70%
Skin irritation - 0.6416 64.16%
Skin corrosion - 0.8383 83.83%
Ames mutagenesis - 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8488 84.88%
Micronuclear - 0.7826 78.26%
Hepatotoxicity + 0.5761 57.61%
skin sensitisation - 0.6711 67.11%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity - 0.6000 60.00%
Mitochondrial toxicity - 0.5875 58.75%
Nephrotoxicity + 0.7610 76.10%
Acute Oral Toxicity (c) III 0.6252 62.52%
Estrogen receptor binding - 0.7169 71.69%
Androgen receptor binding - 0.7700 77.00%
Thyroid receptor binding - 0.8898 88.98%
Glucocorticoid receptor binding - 0.9045 90.45%
Aromatase binding - 0.8355 83.55%
PPAR gamma - 0.7921 79.21%
Honey bee toxicity - 0.9344 93.44%
Biodegradation + 0.7000 70.00%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity + 0.8047 80.47%

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 93.68% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.55% 91.11%
CHEMBL2581 P07339 Cathepsin D 89.54% 98.95%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.45% 97.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.64% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.44% 94.45%
CHEMBL253 P34972 Cannabinoid CB2 receptor 86.06% 97.25%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.11% 100.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 84.46% 85.14%
CHEMBL230 P35354 Cyclooxygenase-2 83.88% 89.63%

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.
Vernonia angustifolia

Cross-Links

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PubChem 15609072
LOTUS LTS0274490
wikiData Q105270434