(4E,8Z)-6,6,9-trimethyl-2-methylidenecycloundeca-4,8-dien-1-one

Details

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Internal ID 3262d04f-0ffb-428d-90d2-67d4076d094f
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (4E,8Z)-6,6,9-trimethyl-2-methylidenecycloundeca-4,8-dien-1-one
SMILES (Canonical) CC1=CCC(C=CCC(=C)C(=O)CC1)(C)C
SMILES (Isomeric) C/C/1=C/CC(/C=C/CC(=C)C(=O)CC1)(C)C
InChI InChI=1S/C15H22O/c1-12-7-8-14(16)13(2)6-5-10-15(3,4)11-9-12/h5,9-10H,2,6-8,11H2,1,3-4H3/b10-5+,12-9-
InChI Key ZZYRTNAABNHZCH-UDKPHDTFSA-N
Popularity 0 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 3.90
Atomic LogP (AlogP) 4.21
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (4E,8Z)-6,6,9-trimethyl-2-methylidenecycloundeca-4,8-dien-1-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9952 99.52%
Caco-2 + 0.9336 93.36%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.4958 49.58%
OATP2B1 inhibitior - 0.8520 85.20%
OATP1B1 inhibitior + 0.9338 93.38%
OATP1B3 inhibitior - 0.3740 37.40%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior - 0.8130 81.30%
P-glycoprotein inhibitior - 0.9425 94.25%
P-glycoprotein substrate - 0.9267 92.67%
CYP3A4 substrate + 0.5251 52.51%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8483 84.83%
CYP3A4 inhibition - 0.8808 88.08%
CYP2C9 inhibition - 0.8399 83.99%
CYP2C19 inhibition - 0.7483 74.83%
CYP2D6 inhibition - 0.9506 95.06%
CYP1A2 inhibition - 0.6517 65.17%
CYP2C8 inhibition - 0.9125 91.25%
CYP inhibitory promiscuity - 0.8963 89.63%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8200 82.00%
Carcinogenicity (trinary) Non-required 0.5241 52.41%
Eye corrosion - 0.8987 89.87%
Eye irritation + 0.8727 87.27%
Skin irritation + 0.6816 68.16%
Skin corrosion - 0.9760 97.60%
Ames mutagenesis - 0.6900 69.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4170 41.70%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.8000 80.00%
skin sensitisation + 0.8931 89.31%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity - 0.6667 66.67%
Mitochondrial toxicity - 0.8000 80.00%
Nephrotoxicity + 0.8376 83.76%
Acute Oral Toxicity (c) III 0.6574 65.74%
Estrogen receptor binding - 0.8888 88.88%
Androgen receptor binding - 0.8567 85.67%
Thyroid receptor binding - 0.7077 70.77%
Glucocorticoid receptor binding - 0.7905 79.05%
Aromatase binding - 0.6056 60.56%
PPAR gamma - 0.5287 52.87%
Honey bee toxicity - 0.8908 89.08%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity + 0.9838 98.38%

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 92.45% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.11% 91.11%
CHEMBL2581 P07339 Cathepsin D 88.58% 98.95%
CHEMBL1871 P10275 Androgen Receptor 83.52% 96.43%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.80% 94.45%

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.
Gelsemium elegans
Humulus lupulus

Cross-Links

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PubChem 5318099
NPASS NPC41448