1,4,4,8-Tetramethylcycloundeca-2,8-dien-1-ol

Details

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Internal ID ed4de57a-b21d-4dfc-bd74-8f2120817491
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 1,4,4,8-tetramethylcycloundeca-2,8-dien-1-ol
SMILES (Canonical) CC1=CCCC(C=CC(CCC1)(C)C)(C)O
SMILES (Isomeric) CC1=CCCC(C=CC(CCC1)(C)C)(C)O
InChI InChI=1S/C15H26O/c1-13-7-5-9-14(2,3)11-12-15(4,16)10-6-8-13/h8,11-12,16H,5-7,9-10H2,1-4H3
InChI Key FZPDSGOTYHMYJT-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H26O
Molecular Weight 222.37 g/mol
Exact Mass 222.198365449 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 4.10
Atomic LogP (AlogP) 4.23
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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1,4,4,8-tetramethylcycloundeca-2,8-dien-1-ol
DTXSID80766677

2D Structure

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2D Structure of 1,4,4,8-Tetramethylcycloundeca-2,8-dien-1-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9968 99.68%
Caco-2 + 0.9507 95.07%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Lysosomes 0.4231 42.31%
OATP2B1 inhibitior - 0.8483 84.83%
OATP1B1 inhibitior + 0.9491 94.91%
OATP1B3 inhibitior + 0.9624 96.24%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.5906 59.06%
P-glycoprotein inhibitior - 0.9586 95.86%
P-glycoprotein substrate - 0.9521 95.21%
CYP3A4 substrate - 0.5827 58.27%
CYP2C9 substrate - 0.7795 77.95%
CYP2D6 substrate - 0.7954 79.54%
CYP3A4 inhibition - 0.8491 84.91%
CYP2C9 inhibition - 0.8021 80.21%
CYP2C19 inhibition - 0.8452 84.52%
CYP2D6 inhibition - 0.9424 94.24%
CYP1A2 inhibition - 0.7819 78.19%
CYP2C8 inhibition - 0.8826 88.26%
CYP inhibitory promiscuity - 0.9170 91.70%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.8128 81.28%
Carcinogenicity (trinary) Non-required 0.5904 59.04%
Eye corrosion - 0.9038 90.38%
Eye irritation + 0.9219 92.19%
Skin irritation + 0.7754 77.54%
Skin corrosion - 0.9561 95.61%
Ames mutagenesis - 0.8070 80.70%
Human Ether-a-go-go-Related Gene inhibition - 0.5844 58.44%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.5235 52.35%
skin sensitisation + 0.8315 83.15%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity - 0.6889 68.89%
Mitochondrial toxicity - 0.6625 66.25%
Nephrotoxicity + 0.5132 51.32%
Acute Oral Toxicity (c) III 0.7956 79.56%
Estrogen receptor binding - 0.8910 89.10%
Androgen receptor binding - 0.8283 82.83%
Thyroid receptor binding - 0.5863 58.63%
Glucocorticoid receptor binding - 0.6630 66.30%
Aromatase binding - 0.7622 76.22%
PPAR gamma - 0.7465 74.65%
Honey bee toxicity - 0.9617 96.17%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity + 0.8948 89.48%

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 91.31% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.65% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.12% 95.56%
CHEMBL4208 P20618 Proteasome component C5 85.62% 90.00%
CHEMBL2581 P07339 Cathepsin D 84.83% 98.95%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.10% 100.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.96% 94.45%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 81.11% 95.50%

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.
Abies alba

Cross-Links

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PubChem 71339198
LOTUS LTS0001585
wikiData Q82724223