2,6,6,9-Tetramethyl-3-methylidenecycloundeca-1,4,8-triene

Details

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Internal ID f2ab3634-3d32-4366-b9a9-9064c91c4331
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 2,6,6,9-tetramethyl-3-methylidenecycloundeca-1,4,8-triene
SMILES (Canonical) CC1=CCC(C=CC(=C)C(=CCC1)C)(C)C
SMILES (Isomeric) CC1=CCC(C=CC(=C)C(=CCC1)C)(C)C
InChI InChI=1S/C16H24/c1-13-7-6-8-14(2)15(3)10-12-16(4,5)11-9-13/h8-10,12H,3,6-7,11H2,1-2,4-5H3
InChI Key ZBPBPXWKBXSESR-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C16H24
Molecular Weight 216.36 g/mol
Exact Mass 216.187800766 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 4.70
Atomic LogP (AlogP) 5.20
H-Bond Acceptor 0
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 2,6,6,9-Tetramethyl-3-methylidenecycloundeca-1,4,8-triene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9892 98.92%
Caco-2 + 0.9551 95.51%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.7429 74.29%
Subcellular localzation Lysosomes 0.6452 64.52%
OATP2B1 inhibitior - 0.8573 85.73%
OATP1B1 inhibitior + 0.9529 95.29%
OATP1B3 inhibitior + 0.8196 81.96%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior - 0.7732 77.32%
P-glycoprotein inhibitior - 0.9552 95.52%
P-glycoprotein substrate - 0.9163 91.63%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7984 79.84%
CYP3A4 inhibition - 0.8968 89.68%
CYP2C9 inhibition - 0.7957 79.57%
CYP2C19 inhibition - 0.7617 76.17%
CYP2D6 inhibition - 0.9453 94.53%
CYP1A2 inhibition - 0.7562 75.62%
CYP2C8 inhibition - 0.7779 77.79%
CYP inhibitory promiscuity - 0.7305 73.05%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6700 67.00%
Carcinogenicity (trinary) Warning 0.4740 47.40%
Eye corrosion - 0.8116 81.16%
Eye irritation + 0.9768 97.68%
Skin irritation + 0.5797 57.97%
Skin corrosion - 0.9853 98.53%
Ames mutagenesis - 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6833 68.33%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.7125 71.25%
skin sensitisation + 0.8704 87.04%
Respiratory toxicity - 0.6667 66.67%
Reproductive toxicity - 0.6778 67.78%
Mitochondrial toxicity - 0.5500 55.00%
Nephrotoxicity + 0.6892 68.92%
Acute Oral Toxicity (c) III 0.7467 74.67%
Estrogen receptor binding - 0.8791 87.91%
Androgen receptor binding - 0.8097 80.97%
Thyroid receptor binding - 0.6863 68.63%
Glucocorticoid receptor binding - 0.7807 78.07%
Aromatase binding - 0.5288 52.88%
PPAR gamma - 0.6237 62.37%
Honey bee toxicity - 0.9296 92.96%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity + 0.6300 63.00%
Fish aquatic toxicity + 1.0000 100.00%

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 93.68% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.28% 95.56%
CHEMBL5966 P55899 IgG receptor FcRn large subunit p51 83.25% 90.93%
CHEMBL1871 P10275 Androgen Receptor 82.12% 96.43%
CHEMBL3192 Q9BY41 Histone deacetylase 8 80.85% 93.99%

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 162866320
LOTUS LTS0211715
wikiData Q105370761