2,6,6-Trimethylcycloundeca-1,4-diene

Details

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Internal ID a4ea8c18-2869-45e8-992d-516f3fbeafc6
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Branched unsaturated hydrocarbons
IUPAC Name 2,6,6-trimethylcycloundeca-1,4-diene
SMILES (Canonical) CC1=CCCCCCC(C=CC1)(C)C
SMILES (Isomeric) CC1=CCCCCCC(C=CC1)(C)C
InChI InChI=1S/C14H24/c1-13-9-6-4-5-7-11-14(2,3)12-8-10-13/h8-9,12H,4-7,10-11H2,1-3H3
InChI Key FUMXJXCOEIVRTP-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C14H24
Molecular Weight 192.34 g/mol
Exact Mass 192.187800766 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 5.40
Atomic LogP (AlogP) 4.87
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-Trimethylcycloundeca-1,4-diene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9907 99.07%
Caco-2 + 0.9795 97.95%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.7429 74.29%
Subcellular localzation Lysosomes 0.5788 57.88%
OATP2B1 inhibitior - 0.8533 85.33%
OATP1B1 inhibitior + 0.9169 91.69%
OATP1B3 inhibitior + 0.9480 94.80%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.7383 73.83%
P-glycoprotein inhibitior - 0.9752 97.52%
P-glycoprotein substrate - 0.9630 96.30%
CYP3A4 substrate - 0.5698 56.98%
CYP2C9 substrate - 0.8038 80.38%
CYP2D6 substrate - 0.7848 78.48%
CYP3A4 inhibition - 0.9106 91.06%
CYP2C9 inhibition - 0.7994 79.94%
CYP2C19 inhibition - 0.7952 79.52%
CYP2D6 inhibition - 0.9406 94.06%
CYP1A2 inhibition - 0.8014 80.14%
CYP2C8 inhibition - 0.8894 88.94%
CYP inhibitory promiscuity - 0.7646 76.46%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6600 66.00%
Carcinogenicity (trinary) Warning 0.5028 50.28%
Eye corrosion - 0.6888 68.88%
Eye irritation + 0.9167 91.67%
Skin irritation + 0.6995 69.95%
Skin corrosion - 0.9762 97.62%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4428 44.28%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.5772 57.72%
skin sensitisation + 0.9074 90.74%
Respiratory toxicity - 0.7444 74.44%
Reproductive toxicity - 0.7222 72.22%
Mitochondrial toxicity + 0.5125 51.25%
Nephrotoxicity - 0.6595 65.95%
Acute Oral Toxicity (c) III 0.6889 68.89%
Estrogen receptor binding - 0.9487 94.87%
Androgen receptor binding - 0.9103 91.03%
Thyroid receptor binding - 0.7545 75.45%
Glucocorticoid receptor binding - 0.8311 83.11%
Aromatase binding - 0.7855 78.55%
PPAR gamma - 0.8841 88.41%
Honey bee toxicity - 0.9510 95.10%
Biodegradation + 0.6000 60.00%
Crustacea aquatic toxicity + 0.6400 64.00%
Fish aquatic toxicity + 0.9940 99.40%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 86.86% 97.25%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.70% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.23% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.04% 96.09%
CHEMBL2581 P07339 Cathepsin D 83.22% 98.95%
CHEMBL3012 Q13946 Phosphodiesterase 7A 82.88% 99.29%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 82.76% 86.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 80.72% 91.11%

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.
Zieria aspalathoides

Cross-Links

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PubChem 163016794
LOTUS LTS0012556
wikiData Q105001839