3-(1,1-dihydroxyethyl)-4-penta-1,3-dienyl-2H-furan-5-one

Details

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Internal ID b38ad55c-74ab-4cfa-aec1-d899825ed1c2
Taxonomy Organoheterocyclic compounds > Dihydrofurans > Furanones > Butenolides
IUPAC Name 3-(1,1-dihydroxyethyl)-4-penta-1,3-dienyl-2H-furan-5-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C11H14O4/c1-3-4-5-6-8-9(11(2,13)14)7-15-10(8)12/h3-6,13-14H,7H2,1-2H3
InChI Key QDTFECJFZJEECZ-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C11H14O4
Molecular Weight 210.23 g/mol
Exact Mass 210.08920892 g/mol
Topological Polar Surface Area (TPSA) 66.80 Ų
XlogP 0.20
Atomic LogP (AlogP) 0.67
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3-(1,1-dihydroxyethyl)-4-penta-1,3-dienyl-2H-furan-5-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9656 96.56%
Caco-2 + 0.6272 62.72%
Blood Brain Barrier + 0.5928 59.28%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.7564 75.64%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9383 93.83%
OATP1B3 inhibitior + 0.9579 95.79%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.8596 85.96%
P-glycoprotein inhibitior - 0.9783 97.83%
P-glycoprotein substrate - 0.9516 95.16%
CYP3A4 substrate - 0.5748 57.48%
CYP2C9 substrate - 0.8062 80.62%
CYP2D6 substrate - 0.8887 88.87%
CYP3A4 inhibition - 0.9395 93.95%
CYP2C9 inhibition - 0.8635 86.35%
CYP2C19 inhibition - 0.8497 84.97%
CYP2D6 inhibition - 0.9387 93.87%
CYP1A2 inhibition - 0.7229 72.29%
CYP2C8 inhibition - 0.9660 96.60%
CYP inhibitory promiscuity - 0.8626 86.26%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9228 92.28%
Carcinogenicity (trinary) Non-required 0.6539 65.39%
Eye corrosion - 0.9443 94.43%
Eye irritation + 0.5396 53.96%
Skin irritation - 0.5749 57.49%
Skin corrosion - 0.8799 87.99%
Ames mutagenesis + 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6982 69.82%
Micronuclear - 0.6300 63.00%
Hepatotoxicity + 0.7375 73.75%
skin sensitisation - 0.7903 79.03%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity + 0.5111 51.11%
Mitochondrial toxicity - 0.5625 56.25%
Nephrotoxicity + 0.7752 77.52%
Acute Oral Toxicity (c) III 0.5154 51.54%
Estrogen receptor binding - 0.7858 78.58%
Androgen receptor binding - 0.6842 68.42%
Thyroid receptor binding - 0.7381 73.81%
Glucocorticoid receptor binding - 0.5791 57.91%
Aromatase binding - 0.7334 73.34%
PPAR gamma + 0.5222 52.22%
Honey bee toxicity - 0.9378 93.78%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 0.9005 90.05%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.25% 95.56%
CHEMBL2581 P07339 Cathepsin D 92.07% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 90.39% 94.73%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.20% 91.11%
CHEMBL2039 P27338 Monoamine oxidase B 89.17% 92.51%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 84.76% 85.14%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.06% 89.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.01% 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 85185908
LOTUS LTS0048318
wikiData Q104195705