5-(E)-But-2-enylidene-3-(E)-propenyl-5H-furan-2-one

Details

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Internal ID c9769202-dbf2-4769-834f-16fe9ea2655b
Taxonomy Organoheterocyclic compounds > Dihydrofurans > Furanones > Butenolides
IUPAC Name (5E)-5-[(E)-but-2-enylidene]-3-[(E)-prop-1-enyl]furan-2-one
SMILES (Canonical) CC=CC=C1C=C(C(=O)O1)C=CC
SMILES (Isomeric) C/C=C/C=C/1\C=C(C(=O)O1)/C=C/C
InChI InChI=1S/C11H12O2/c1-3-5-7-10-8-9(6-4-2)11(12)13-10/h3-8H,1-2H3/b5-3+,6-4+,10-7+
InChI Key UTMKJYVBEKRSSY-FQXJPFFWSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C11H12O2
Molecular Weight 176.21 g/mol
Exact Mass 176.083729621 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 2.70
Atomic LogP (AlogP) 2.51
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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(5E)-5-((E)-but-2-enylidene)-3-((E)-prop-1-enyl)furan-2-one
(5E)-5-[(E)-but-2-enylidene]-3-[(E)-prop-1-enyl]furan-2-one
RefChem:101792
CHEBI:212892
(5E)-5-[(E)-but-2-enylidene]-3-[(E)-prop-1-enyl]uran-2-one

2D Structure

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2D Structure of 5-(E)-But-2-enylidene-3-(E)-propenyl-5H-furan-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 + 0.9970 99.70%
Caco-2 + 0.8504 85.04%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability + 0.7571 75.71%
Subcellular localzation Mitochondria 0.6600 66.00%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8850 88.50%
OATP1B3 inhibitior + 0.9661 96.61%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.7133 71.33%
P-glycoprotein inhibitior - 0.9629 96.29%
P-glycoprotein substrate - 0.9538 95.38%
CYP3A4 substrate - 0.6092 60.92%
CYP2C9 substrate - 0.5979 59.79%
CYP2D6 substrate - 0.8704 87.04%
CYP3A4 inhibition - 0.9566 95.66%
CYP2C9 inhibition - 0.9578 95.78%
CYP2C19 inhibition - 0.8018 80.18%
CYP2D6 inhibition - 0.9572 95.72%
CYP1A2 inhibition - 0.7527 75.27%
CYP2C8 inhibition - 0.9312 93.12%
CYP inhibitory promiscuity - 0.5324 53.24%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8244 82.44%
Carcinogenicity (trinary) Non-required 0.4362 43.62%
Eye corrosion + 0.7153 71.53%
Eye irritation + 0.9778 97.78%
Skin irritation + 0.6756 67.56%
Skin corrosion - 0.8143 81.43%
Ames mutagenesis - 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6547 65.47%
Micronuclear + 0.5500 55.00%
Hepatotoxicity + 0.6875 68.75%
skin sensitisation + 0.7081 70.81%
Respiratory toxicity + 0.7111 71.11%
Reproductive toxicity - 0.6333 63.33%
Mitochondrial toxicity - 0.7125 71.25%
Nephrotoxicity + 0.6853 68.53%
Acute Oral Toxicity (c) III 0.7401 74.01%
Estrogen receptor binding - 0.5989 59.89%
Androgen receptor binding - 0.8774 87.74%
Thyroid receptor binding - 0.6677 66.77%
Glucocorticoid receptor binding - 0.8547 85.47%
Aromatase binding + 0.5741 57.41%
PPAR gamma - 0.8042 80.42%
Honey bee toxicity - 0.9029 90.29%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity + 0.5800 58.00%
Fish aquatic toxicity + 0.7632 76.32%

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
CHEMBL2581 P07339 Cathepsin D 92.37% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.13% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.46% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 86.71% 94.73%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.04% 91.11%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.15% 99.23%

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 139587167
LOTUS LTS0141185
wikiData Q77559494