Zerumbodienone

Details

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Internal ID 865abeaf-34cb-4839-aecb-ba85a70e4de5
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (2Z,10E)-2,6,9,9-tetramethylcycloundeca-2,10-dien-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H24O/c1-12-6-5-7-13(2)14(16)9-11-15(3,4)10-8-12/h7,9,11-12H,5-6,8,10H2,1-4H3/b11-9+,13-7-
InChI Key CSYLYPZVYTWHKT-JNLWHAGFSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H24O
Molecular Weight 220.35 g/mol
Exact Mass 220.182715385 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 5.10
Atomic LogP (AlogP) 4.29
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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CSYLYPZVYTWHKT-JNLWHAGFSA-N

2D Structure

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2D Structure of Zerumbodienone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9961 99.61%
Caco-2 + 0.9522 95.22%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.4522 45.22%
OATP2B1 inhibitior - 0.8505 85.05%
OATP1B1 inhibitior + 0.9547 95.47%
OATP1B3 inhibitior + 0.8882 88.82%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.6250 62.50%
BSEP inhibitior - 0.8538 85.38%
P-glycoprotein inhibitior - 0.9399 93.99%
P-glycoprotein substrate - 0.9334 93.34%
CYP3A4 substrate + 0.5416 54.16%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8865 88.65%
CYP3A4 inhibition - 0.9226 92.26%
CYP2C9 inhibition - 0.8155 81.55%
CYP2C19 inhibition - 0.7701 77.01%
CYP2D6 inhibition - 0.9448 94.48%
CYP1A2 inhibition - 0.6719 67.19%
CYP2C8 inhibition - 0.9302 93.02%
CYP inhibitory promiscuity - 0.8191 81.91%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8500 85.00%
Carcinogenicity (trinary) Non-required 0.5159 51.59%
Eye corrosion - 0.8938 89.38%
Eye irritation + 0.5370 53.70%
Skin irritation + 0.6905 69.05%
Skin corrosion - 0.9745 97.45%
Ames mutagenesis - 0.7670 76.70%
Human Ether-a-go-go-Related Gene inhibition - 0.4107 41.07%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.6721 67.21%
skin sensitisation + 0.9082 90.82%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity - 0.6556 65.56%
Mitochondrial toxicity - 0.7500 75.00%
Nephrotoxicity + 0.7700 77.00%
Acute Oral Toxicity (c) III 0.6020 60.20%
Estrogen receptor binding - 0.9401 94.01%
Androgen receptor binding - 0.8519 85.19%
Thyroid receptor binding - 0.7356 73.56%
Glucocorticoid receptor binding - 0.8642 86.42%
Aromatase binding - 0.7532 75.32%
PPAR gamma - 0.8625 86.25%
Honey bee toxicity - 0.9380 93.80%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 0.9848 98.48%

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 91.93% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.77% 97.09%
CHEMBL1937 Q92769 Histone deacetylase 2 89.96% 94.75%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 88.67% 86.00%
CHEMBL253 P34972 Cannabinoid CB2 receptor 88.17% 97.25%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 87.65% 93.40%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.38% 100.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.36% 91.11%
CHEMBL2581 P07339 Cathepsin D 84.37% 98.95%
CHEMBL3192 Q9BY41 Histone deacetylase 8 83.12% 93.99%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.56% 96.09%
CHEMBL1871 P10275 Androgen Receptor 81.41% 96.43%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.25% 99.23%
CHEMBL325 Q13547 Histone deacetylase 1 80.12% 95.92%

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.
Zingiber zerumbet

Cross-Links

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PubChem 5463722
LOTUS LTS0093572
wikiData Q104253360