4-decanoyl-5-hydroxy-2-methylidenefuran-3-one

Details

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Internal ID 807f66db-3410-4f12-8f4c-db336a4f7a92
Taxonomy Organoheterocyclic compounds > Dihydrofurans > Furanones
IUPAC Name 4-decanoyl-5-hydroxy-2-methylidenefuran-3-one
SMILES (Canonical) CCCCCCCCCC(=O)C1=C(OC(=C)C1=O)O
SMILES (Isomeric) CCCCCCCCCC(=O)C1=C(OC(=C)C1=O)O
InChI InChI=1S/C15H22O4/c1-3-4-5-6-7-8-9-10-12(16)13-14(17)11(2)19-15(13)18/h18H,2-10H2,1H3
InChI Key VSYFNRKKBJSZBB-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H22O4
Molecular Weight 266.33 g/mol
Exact Mass 266.15180918 g/mol
Topological Polar Surface Area (TPSA) 63.60 Ų
XlogP 5.10
Atomic LogP (AlogP) 3.58
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 9

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4-decanoyl-5-hydroxy-2-methylidenefuran-3-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9495 94.95%
Caco-2 + 0.5195 51.95%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.7014 70.14%
OATP2B1 inhibitior - 0.8516 85.16%
OATP1B1 inhibitior + 0.8225 82.25%
OATP1B3 inhibitior + 0.9297 92.97%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.8032 80.32%
P-glycoprotein inhibitior - 0.8975 89.75%
P-glycoprotein substrate - 0.8455 84.55%
CYP3A4 substrate - 0.5642 56.42%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8551 85.51%
CYP3A4 inhibition - 0.6323 63.23%
CYP2C9 inhibition - 0.8536 85.36%
CYP2C19 inhibition - 0.6312 63.12%
CYP2D6 inhibition - 0.8944 89.44%
CYP1A2 inhibition - 0.6059 60.59%
CYP2C8 inhibition - 0.8767 87.67%
CYP inhibitory promiscuity - 0.9019 90.19%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.6339 63.39%
Eye corrosion - 0.9633 96.33%
Eye irritation + 0.9077 90.77%
Skin irritation + 0.6204 62.04%
Skin corrosion - 0.8893 88.93%
Ames mutagenesis - 0.9400 94.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7054 70.54%
Micronuclear - 0.9200 92.00%
Hepatotoxicity + 0.5500 55.00%
skin sensitisation - 0.8378 83.78%
Respiratory toxicity - 0.6778 67.78%
Reproductive toxicity - 0.5667 56.67%
Mitochondrial toxicity - 0.5250 52.50%
Nephrotoxicity + 0.7398 73.98%
Acute Oral Toxicity (c) III 0.5831 58.31%
Estrogen receptor binding - 0.7150 71.50%
Androgen receptor binding - 0.5894 58.94%
Thyroid receptor binding + 0.5178 51.78%
Glucocorticoid receptor binding - 0.6576 65.76%
Aromatase binding - 0.6092 60.92%
PPAR gamma + 0.7303 73.03%
Honey bee toxicity - 0.9778 97.78%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity + 0.7468 74.68%
Fish aquatic toxicity + 0.9929 99.29%

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 95.15% 98.95%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 95.15% 95.17%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.50% 99.17%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 90.35% 99.23%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.17% 91.11%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 88.33% 92.08%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 87.16% 85.94%
CHEMBL3401 O75469 Pregnane X receptor 86.78% 94.73%
CHEMBL230 P35354 Cyclooxygenase-2 85.49% 89.63%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.48% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 81.36% 96.09%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 80.48% 90.71%

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 130485
LOTUS LTS0202224
wikiData Q105292601