3,11,11-Trimethylbicyclo[8.1.0]undeca-2,6-diene

Details

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Internal ID eb18f003-d604-4e9e-8262-99193dfffd21
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Branched unsaturated hydrocarbons
IUPAC Name 3,11,11-trimethylbicyclo[8.1.0]undeca-2,6-diene
SMILES (Canonical) CC1=CC2C(C2(C)C)CCC=CCC1
SMILES (Isomeric) CC1=CC2C(C2(C)C)CCC=CCC1
InChI InChI=1S/C14H22/c1-11-8-6-4-5-7-9-12-13(10-11)14(12,2)3/h4-5,10,12-13H,6-9H2,1-3H3
InChI Key UHDKBUSKUVYWQE-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 4.20
Atomic LogP (AlogP) 4.34
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 3,11,11-Trimethylbicyclo[8.1.0]undeca-2,6-diene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9909 99.09%
Caco-2 + 0.8792 87.92%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.7714 77.14%
Subcellular localzation Lysosomes 0.6555 65.55%
OATP2B1 inhibitior - 0.8531 85.31%
OATP1B1 inhibitior + 0.9475 94.75%
OATP1B3 inhibitior + 0.9624 96.24%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.8447 84.47%
P-glycoprotein inhibitior - 0.9182 91.82%
P-glycoprotein substrate - 0.9384 93.84%
CYP3A4 substrate + 0.5144 51.44%
CYP2C9 substrate - 0.7947 79.47%
CYP2D6 substrate - 0.7615 76.15%
CYP3A4 inhibition - 0.8991 89.91%
CYP2C9 inhibition - 0.6993 69.93%
CYP2C19 inhibition - 0.6402 64.02%
CYP2D6 inhibition - 0.9299 92.99%
CYP1A2 inhibition - 0.6910 69.10%
CYP2C8 inhibition - 0.8461 84.61%
CYP inhibitory promiscuity - 0.7842 78.42%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6700 67.00%
Carcinogenicity (trinary) Warning 0.4661 46.61%
Eye corrosion - 0.8501 85.01%
Eye irritation - 0.8639 86.39%
Skin irritation + 0.6803 68.03%
Skin corrosion - 0.9651 96.51%
Ames mutagenesis - 0.8500 85.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6476 64.76%
Micronuclear - 0.8900 89.00%
Hepatotoxicity + 0.5750 57.50%
skin sensitisation + 0.8733 87.33%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity - 0.7667 76.67%
Mitochondrial toxicity + 0.5750 57.50%
Nephrotoxicity + 0.4656 46.56%
Acute Oral Toxicity (c) III 0.7166 71.66%
Estrogen receptor binding - 0.9185 91.85%
Androgen receptor binding - 0.7117 71.17%
Thyroid receptor binding - 0.7689 76.89%
Glucocorticoid receptor binding - 0.7413 74.13%
Aromatase binding - 0.8553 85.53%
PPAR gamma - 0.8385 83.85%
Honey bee toxicity - 0.8668 86.68%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity + 0.8200 82.00%
Fish aquatic toxicity + 0.9941 99.41%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.96% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.69% 91.11%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.81% 100.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.03% 97.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 84.60% 97.25%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.49% 95.56%
CHEMBL2996 Q05655 Protein kinase C delta 83.10% 97.79%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.08% 95.89%
CHEMBL1871 P10275 Androgen Receptor 80.65% 96.43%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 80.26% 86.00%

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.
Helichrysum glomeratum

Cross-Links

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PubChem 162901795
LOTUS LTS0268473
wikiData Q105272721