6,6,9-Trimethylcycloundeca-1,4,8-triene

Details

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Internal ID ad786d6b-ff48-46c5-ae2d-c830a785c749
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Branched unsaturated hydrocarbons
IUPAC Name 6,6,9-trimethylcycloundeca-1,4,8-triene
SMILES (Canonical) CC1=CCC(C=CCC=CCC1)(C)C
SMILES (Isomeric) CC1=CCC(C=CCC=CCC1)(C)C
InChI InChI=1S/C14H22/c1-13-9-7-5-4-6-8-11-14(2,3)12-10-13/h4-5,8,10-11H,6-7,9,12H2,1-3H3
InChI Key PSVBPLKYDMHILE-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C14H22
Molecular Weight 190.32 g/mol
Exact Mass 190.172150702 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 4.60
Atomic LogP (AlogP) 4.65
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 6,6,9-Trimethylcycloundeca-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 + 0.9907 99.07%
Caco-2 + 0.9384 93.84%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.7714 77.14%
Subcellular localzation Lysosomes 0.5788 57.88%
OATP2B1 inhibitior - 0.8559 85.59%
OATP1B1 inhibitior + 0.9583 95.83%
OATP1B3 inhibitior + 0.9480 94.80%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.7911 79.11%
P-glycoprotein inhibitior - 0.9764 97.64%
P-glycoprotein substrate - 0.9442 94.42%
CYP3A4 substrate - 0.5598 55.98%
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 - 0.8950 89.50%
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 + 0.9361 93.61%
Skin irritation + 0.6995 69.95%
Skin corrosion - 0.9762 97.62%
Ames mutagenesis - 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4184 41.84%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.7065 70.65%
skin sensitisation + 0.9074 90.74%
Respiratory toxicity - 0.7000 70.00%
Reproductive toxicity - 0.7222 72.22%
Mitochondrial toxicity + 0.5125 51.25%
Nephrotoxicity + 0.7321 73.21%
Acute Oral Toxicity (c) III 0.6889 68.89%
Estrogen receptor binding - 0.9419 94.19%
Androgen receptor binding - 0.9068 90.68%
Thyroid receptor binding - 0.7683 76.83%
Glucocorticoid receptor binding - 0.8525 85.25%
Aromatase binding - 0.7671 76.71%
PPAR gamma - 0.7929 79.29%
Honey bee toxicity - 0.9328 93.28%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity + 0.6800 68.00%
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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.21% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.95% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.93% 95.56%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 80.94% 85.30%
CHEMBL4208 P20618 Proteasome component C5 80.77% 90.00%
CHEMBL1871 P10275 Androgen Receptor 80.58% 96.43%

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.
Caputia tomentosa

Cross-Links

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PubChem 162862437
LOTUS LTS0217287
wikiData Q105214409