2(5H)-Furanone, 5-(4-hydroxy-2-butenylidene)-3-(3-hydroxy-1-propenyl)-, (Z,E,E)-

Details

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Internal ID ae7c13ce-a939-4b91-aa2b-1e06617bae5a
Taxonomy Organoheterocyclic compounds > Dihydrofurans > Furanones > Butenolides
IUPAC Name (5E)-5-[(E)-4-hydroxybut-2-enylidene]-3-[(Z)-3-hydroxyprop-1-enyl]furan-2-one
SMILES (Canonical) C1=C(C(=O)OC1=CC=CCO)C=CCO
SMILES (Isomeric) C\1=C(C(=O)O/C1=C/C=C/CO)/C=C\CO
InChI InChI=1S/C11H12O4/c12-6-2-1-5-10-8-9(4-3-7-13)11(14)15-10/h1-5,8,12-13H,6-7H2/b2-1+,4-3-,10-5+
InChI Key ZYNGLDJNLYFSIV-KKHLZRMGSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C11H12O4
Molecular Weight 208.21 g/mol
Exact Mass 208.07355886 g/mol
Topological Polar Surface Area (TPSA) 66.80 Ų
XlogP 0.20
Atomic LogP (AlogP) 0.45
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

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(5E)-5-[(E)-4-hydroxybut-2-enylidene]-3-[(Z)-3-hydroxyprop-1-enyl]furan-2-one
2(5H)-Furanone, 5-(4-hydroxy-2-butenylidene)-3-(3-hydroxy-1-propenyl)-, (Z,E,E)-

2D Structure

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2D Structure of 2(5H)-Furanone, 5-(4-hydroxy-2-butenylidene)-3-(3-hydroxy-1-propenyl)-, (Z,E,E)-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9537 95.37%
Caco-2 + 0.7224 72.24%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.7378 73.78%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8744 87.44%
OATP1B3 inhibitior + 0.9481 94.81%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.8531 85.31%
P-glycoprotein inhibitior - 0.9734 97.34%
P-glycoprotein substrate - 0.9714 97.14%
CYP3A4 substrate - 0.6226 62.26%
CYP2C9 substrate - 0.5947 59.47%
CYP2D6 substrate - 0.8520 85.20%
CYP3A4 inhibition - 0.9612 96.12%
CYP2C9 inhibition - 0.8736 87.36%
CYP2C19 inhibition - 0.8224 82.24%
CYP2D6 inhibition - 0.9232 92.32%
CYP1A2 inhibition - 0.7575 75.75%
CYP2C8 inhibition - 0.9220 92.20%
CYP inhibitory promiscuity - 0.6977 69.77%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.8744 87.44%
Carcinogenicity (trinary) Non-required 0.5485 54.85%
Eye corrosion - 0.8781 87.81%
Eye irritation + 0.9686 96.86%
Skin irritation - 0.5541 55.41%
Skin corrosion - 0.7798 77.98%
Ames mutagenesis - 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7291 72.91%
Micronuclear - 0.6200 62.00%
Hepatotoxicity - 0.5375 53.75%
skin sensitisation - 0.7572 75.72%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity - 0.5000 50.00%
Mitochondrial toxicity - 0.6875 68.75%
Nephrotoxicity + 0.6287 62.87%
Acute Oral Toxicity (c) III 0.5866 58.66%
Estrogen receptor binding + 0.7720 77.20%
Androgen receptor binding - 0.8566 85.66%
Thyroid receptor binding - 0.6244 62.44%
Glucocorticoid receptor binding - 0.6693 66.93%
Aromatase binding + 0.6629 66.29%
PPAR gamma + 0.6874 68.74%
Honey bee toxicity - 0.9420 94.20%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity - 0.7200 72.00%
Fish aquatic toxicity - 0.3938 39.38%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.37% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.25% 95.56%
CHEMBL2581 P07339 Cathepsin D 86.63% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.01% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 82.78% 94.73%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 81.13% 89.34%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.11% 96.00%

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.
Fagopyrum megacarpum
Quercus robur

Cross-Links

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PubChem 6439327
LOTUS LTS0018142
wikiData Q105001860