3-(4-Methylpent-3-enylidene)oxolan-2-one

Details

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Internal ID 5e8a55db-4c95-4142-96f0-b973a540ffd7
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene lactones
IUPAC Name 3-(4-methylpent-3-enylidene)oxolan-2-one
SMILES (Canonical) CC(=CCC=C1CCOC1=O)C
SMILES (Isomeric) CC(=CCC=C1CCOC1=O)C
InChI InChI=1S/C10H14O2/c1-8(2)4-3-5-9-6-7-12-10(9)11/h4-5H,3,6-7H2,1-2H3
InChI Key CPLJYHROMJLAPW-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C10H14O2
Molecular Weight 166.22 g/mol
Exact Mass 166.099379685 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 2.50
Atomic LogP (AlogP) 2.22
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3-(4-Methylpent-3-enylidene)oxolan-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 + 0.9967 99.67%
Caco-2 + 0.8876 88.76%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.7145 71.45%
OATP2B1 inhibitior - 0.8613 86.13%
OATP1B1 inhibitior + 0.9480 94.80%
OATP1B3 inhibitior + 0.9335 93.35%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.6000 60.00%
BSEP inhibitior - 0.8168 81.68%
P-glycoprotein inhibitior - 0.9898 98.98%
P-glycoprotein substrate - 0.9708 97.08%
CYP3A4 substrate - 0.6211 62.11%
CYP2C9 substrate + 0.5981 59.81%
CYP2D6 substrate - 0.8849 88.49%
CYP3A4 inhibition - 0.9531 95.31%
CYP2C9 inhibition - 0.9171 91.71%
CYP2C19 inhibition - 0.8314 83.14%
CYP2D6 inhibition - 0.9061 90.61%
CYP1A2 inhibition - 0.6391 63.91%
CYP2C8 inhibition - 0.9883 98.83%
CYP inhibitory promiscuity - 0.7947 79.47%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9028 90.28%
Carcinogenicity (trinary) Non-required 0.6883 68.83%
Eye corrosion - 0.6972 69.72%
Eye irritation + 0.9742 97.42%
Skin irritation - 0.5771 57.71%
Skin corrosion - 0.9583 95.83%
Ames mutagenesis - 0.6781 67.81%
Human Ether-a-go-go-Related Gene inhibition - 0.6865 68.65%
Micronuclear - 0.9200 92.00%
Hepatotoxicity + 0.6033 60.33%
skin sensitisation - 0.5787 57.87%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity - 0.7111 71.11%
Mitochondrial toxicity - 0.8000 80.00%
Nephrotoxicity + 0.6384 63.84%
Acute Oral Toxicity (c) III 0.7576 75.76%
Estrogen receptor binding - 0.9555 95.55%
Androgen receptor binding - 0.6895 68.95%
Thyroid receptor binding - 0.8913 89.13%
Glucocorticoid receptor binding - 0.8593 85.93%
Aromatase binding - 0.7876 78.76%
PPAR gamma - 0.7747 77.47%
Honey bee toxicity - 0.9466 94.66%
Biodegradation + 0.7000 70.00%
Crustacea aquatic toxicity - 0.7200 72.00%
Fish aquatic toxicity + 0.9612 96.12%

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 94.74% 91.11%
CHEMBL2581 P07339 Cathepsin D 94.65% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 93.83% 85.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.41% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 89.82% 94.73%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.01% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.64% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 81.67% 96.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.05% 100.00%

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 85762279
LOTUS LTS0187987
wikiData Q104967633