1,5,8,8-Tetramethylcycloundeca-1,5-diene

Details

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Internal ID 3e6980b6-d659-4cd3-8b25-b1e596918faa
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 1,5,8,8-tetramethylcycloundeca-1,5-diene
SMILES (Canonical) CC1=CCCC(=CCC(CCC1)(C)C)C
SMILES (Isomeric) CC1=CCCC(=CCC(CCC1)(C)C)C
InChI InChI=1S/C15H26/c1-13-7-5-8-14(2)10-12-15(3,4)11-6-9-13/h7,10H,5-6,8-9,11-12H2,1-4H3
InChI Key WAAMRUBBXSLLEE-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H26
Molecular Weight 206.37 g/mol
Exact Mass 206.203450829 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 4.90
Atomic LogP (AlogP) 5.26
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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1,5,8,8-Tetramethylcycloundeca-1,5-diene
DTXSID10748365

2D Structure

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2D Structure of 1,5,8,8-Tetramethylcycloundeca-1,5-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 + 0.9772 97.72%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.7571 75.71%
Subcellular localzation Lysosomes 0.5788 57.88%
OATP2B1 inhibitior - 0.8481 84.81%
OATP1B1 inhibitior + 0.9554 95.54%
OATP1B3 inhibitior + 0.9480 94.80%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.6078 60.78%
P-glycoprotein inhibitior - 0.9465 94.65%
P-glycoprotein substrate - 0.9647 96.47%
CYP3A4 substrate - 0.6059 60.59%
CYP2C9 substrate - 0.8058 80.58%
CYP2D6 substrate - 0.7808 78.08%
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 - 0.9068 90.68%
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 + 0.9329 93.29%
Skin irritation + 0.6995 69.95%
Skin corrosion - 0.9762 97.62%
Ames mutagenesis - 0.8664 86.64%
Human Ether-a-go-go-Related Gene inhibition + 0.6617 66.17%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.5091 50.91%
skin sensitisation + 0.9074 90.74%
Respiratory toxicity - 0.6778 67.78%
Reproductive toxicity - 0.7222 72.22%
Mitochondrial toxicity + 0.5125 51.25%
Nephrotoxicity - 0.6120 61.20%
Acute Oral Toxicity (c) III 0.6889 68.89%
Estrogen receptor binding - 0.9551 95.51%
Androgen receptor binding - 0.8431 84.31%
Thyroid receptor binding - 0.8113 81.13%
Glucocorticoid receptor binding - 0.8356 83.56%
Aromatase binding - 0.7436 74.36%
PPAR gamma - 0.8016 80.16%
Honey bee toxicity - 0.9384 93.84%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity + 0.5400 54.00%
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 92.42% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.52% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 86.84% 97.25%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.11% 95.56%
CHEMBL230 P35354 Cyclooxygenase-2 81.56% 89.63%
CHEMBL2996 Q05655 Protein kinase C delta 80.39% 97.79%
CHEMBL2581 P07339 Cathepsin D 80.37% 98.95%

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.
Frullania inflata

Cross-Links

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PubChem 71318205
LOTUS LTS0000840
wikiData Q82697581