Epoxy-beta-ionone

Details

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Internal ID 09e96257-20e4-451b-8c7f-01058c99fc39
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (E)-2-oxo-4-(2,6,6-trimethylcyclohexen-1-yl)but-3-enal
SMILES (Canonical) CC1=C(C(CCC1)(C)C)C=CC(=O)C=O
SMILES (Isomeric) CC1=C(C(CCC1)(C)C)/C=C/C(=O)C=O
InChI InChI=1S/C13H18O2/c1-10-5-4-8-13(2,3)12(10)7-6-11(15)9-14/h6-7,9H,4-5,8H2,1-3H3/b7-6+
InChI Key AVQIAPJJWFUCIT-VOTSOKGWSA-N
Popularity 6 references in papers

Physical and Chemical Properties

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Molecular Formula C13H18O2
Molecular Weight 206.28 g/mol
Exact Mass 206.130679813 g/mol
Topological Polar Surface Area (TPSA) 34.10 Ų
XlogP 2.60
Atomic LogP (AlogP) 2.84
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Epoxy-beta-ionone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9934 99.34%
Caco-2 + 0.9375 93.75%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.6152 61.52%
OATP2B1 inhibitior - 0.8628 86.28%
OATP1B1 inhibitior - 0.3324 33.24%
OATP1B3 inhibitior + 0.8269 82.69%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.5750 57.50%
BSEP inhibitior - 0.8726 87.26%
P-glycoprotein inhibitior - 0.9858 98.58%
P-glycoprotein substrate - 0.9702 97.02%
CYP3A4 substrate + 0.5212 52.12%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8572 85.72%
CYP3A4 inhibition - 0.9317 93.17%
CYP2C9 inhibition - 0.8069 80.69%
CYP2C19 inhibition - 0.7501 75.01%
CYP2D6 inhibition - 0.9202 92.02%
CYP1A2 inhibition - 0.7807 78.07%
CYP2C8 inhibition - 0.8567 85.67%
CYP inhibitory promiscuity - 0.7527 75.27%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6600 66.00%
Carcinogenicity (trinary) Non-required 0.5709 57.09%
Eye corrosion - 0.9460 94.60%
Eye irritation - 0.5126 51.26%
Skin irritation + 0.7262 72.62%
Skin corrosion - 0.9706 97.06%
Ames mutagenesis - 0.7564 75.64%
Human Ether-a-go-go-Related Gene inhibition - 0.6952 69.52%
Micronuclear - 0.9200 92.00%
Hepatotoxicity + 0.7111 71.11%
skin sensitisation + 0.9162 91.62%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity + 0.6444 64.44%
Mitochondrial toxicity - 0.7625 76.25%
Nephrotoxicity + 0.6875 68.75%
Acute Oral Toxicity (c) III 0.8107 81.07%
Estrogen receptor binding - 0.9291 92.91%
Androgen receptor binding - 0.7579 75.79%
Thyroid receptor binding - 0.7739 77.39%
Glucocorticoid receptor binding - 0.8241 82.41%
Aromatase binding - 0.7977 79.77%
PPAR gamma - 0.8141 81.41%
Honey bee toxicity - 0.9433 94.33%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.7100 71.00%
Fish aquatic toxicity + 0.9748 97.48%

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 93.41% 95.56%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 87.80% 95.50%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.72% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.55% 96.09%
CHEMBL230 P35354 Cyclooxygenase-2 86.76% 89.63%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.25% 86.33%
CHEMBL1870 P28702 Retinoid X receptor beta 85.14% 95.00%
CHEMBL2061 P19793 Retinoid X receptor alpha 83.38% 91.67%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.50% 100.00%
CHEMBL2004 P48443 Retinoid X receptor gamma 80.90% 100.00%

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.
Festuca arundinacea
Stevia rebaudiana
Swertia japonica

Cross-Links

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PubChem 129689900
LOTUS LTS0198571
wikiData Q104253557