Cubebenone

Details

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Internal ID 6afd5f7f-3187-4202-923f-5f58d1665ed2
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (5R,6S,7R,10S)-4,10-dimethyl-7-propan-2-yltricyclo[4.4.0.01,5]dec-3-en-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H22O/c1-8(2)11-6-5-10(4)15-12(16)7-9(3)13(15)14(11)15/h7-8,10-11,13-14H,5-6H2,1-4H3/t10-,11+,13-,14-,15?/m0/s1
InChI Key OZMQICPXNIVENO-UGDUAMEYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H22O
Molecular Weight 218.33 g/mol
Exact Mass 218.167065321 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 3.40
Atomic LogP (AlogP) 3.45
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Cubebenone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9972 99.72%
Caco-2 + 0.7400 74.00%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Lysosomes 0.4767 47.67%
OATP2B1 inhibitior - 0.8561 85.61%
OATP1B1 inhibitior + 0.9433 94.33%
OATP1B3 inhibitior + 0.9568 95.68%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior - 0.9159 91.59%
P-glycoprotein inhibitior - 0.9131 91.31%
P-glycoprotein substrate - 0.8188 81.88%
CYP3A4 substrate - 0.5235 52.35%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8710 87.10%
CYP3A4 inhibition - 0.8866 88.66%
CYP2C9 inhibition - 0.7223 72.23%
CYP2C19 inhibition - 0.5272 52.72%
CYP2D6 inhibition - 0.8892 88.92%
CYP1A2 inhibition - 0.6297 62.97%
CYP2C8 inhibition - 0.9702 97.02%
CYP inhibitory promiscuity - 0.5804 58.04%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.4561 45.61%
Eye corrosion - 0.9738 97.38%
Eye irritation - 0.7802 78.02%
Skin irritation + 0.5975 59.75%
Skin corrosion - 0.9404 94.04%
Ames mutagenesis - 0.8100 81.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4699 46.99%
Micronuclear - 0.8800 88.00%
Hepatotoxicity + 0.6551 65.51%
skin sensitisation + 0.8000 80.00%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity + 0.5333 53.33%
Mitochondrial toxicity - 0.5250 52.50%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) III 0.7301 73.01%
Estrogen receptor binding - 0.5374 53.74%
Androgen receptor binding + 0.6881 68.81%
Thyroid receptor binding - 0.5462 54.62%
Glucocorticoid receptor binding - 0.6388 63.88%
Aromatase binding - 0.8847 88.47%
PPAR gamma - 0.8220 82.20%
Honey bee toxicity - 0.9202 92.02%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity + 0.6300 63.00%
Fish aquatic toxicity + 0.9686 96.86%

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 91.32% 95.56%
CHEMBL2581 P07339 Cathepsin D 90.13% 98.95%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 89.97% 86.00%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 89.47% 94.80%
CHEMBL1937 Q92769 Histone deacetylase 2 86.80% 94.75%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 85.89% 90.71%
CHEMBL1871 P10275 Androgen Receptor 85.36% 96.43%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.19% 96.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.48% 100.00%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 83.11% 96.47%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.04% 99.23%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.95% 91.11%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.80% 95.89%
CHEMBL5103 Q969S8 Histone deacetylase 10 82.34% 90.08%
CHEMBL3192 Q9BY41 Histone deacetylase 8 81.27% 93.99%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.23% 89.00%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 80.51% 93.03%

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 11746097
LOTUS LTS0274286
wikiData Q105203931