(4,4,8-Trimethylcycloundeca-1,5,8-trien-1-yl)methanol

Details

Top
Internal ID 5fa1447b-5b46-4b45-9800-8d46d42fd527
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (4,4,8-trimethylcycloundeca-1,5,8-trien-1-yl)methanol
SMILES (Canonical) CC1=CCCC(=CCC(C=CC1)(C)C)CO
SMILES (Isomeric) CC1=CCCC(=CCC(C=CC1)(C)C)CO
InChI InChI=1S/C15H24O/c1-13-6-4-8-14(12-16)9-11-15(2,3)10-5-7-13/h5-6,9-10,16H,4,7-8,11-12H2,1-3H3
InChI Key LLNVHSDAWLZFEV-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C15H24O
Molecular Weight 220.35 g/mol
Exact Mass 220.182715385 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 3.30
Atomic LogP (AlogP) 4.01
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of (4,4,8-Trimethylcycloundeca-1,5,8-trien-1-yl)methanol

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9908 99.08%
Caco-2 + 0.9521 95.21%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Lysosomes 0.7108 71.08%
OATP2B1 inhibitior - 0.8517 85.17%
OATP1B1 inhibitior + 0.9466 94.66%
OATP1B3 inhibitior + 0.8863 88.63%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.6195 61.95%
P-glycoprotein inhibitior - 0.9713 97.13%
P-glycoprotein substrate - 0.9019 90.19%
CYP3A4 substrate - 0.5190 51.90%
CYP2C9 substrate - 0.8127 81.27%
CYP2D6 substrate - 0.7751 77.51%
CYP3A4 inhibition - 0.7653 76.53%
CYP2C9 inhibition - 0.6620 66.20%
CYP2C19 inhibition - 0.7594 75.94%
CYP2D6 inhibition - 0.9076 90.76%
CYP1A2 inhibition - 0.8458 84.58%
CYP2C8 inhibition - 0.8604 86.04%
CYP inhibitory promiscuity - 0.7083 70.83%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.7728 77.28%
Carcinogenicity (trinary) Non-required 0.6120 61.20%
Eye corrosion - 0.8300 83.00%
Eye irritation + 0.8852 88.52%
Skin irritation - 0.5236 52.36%
Skin corrosion - 0.9637 96.37%
Ames mutagenesis - 0.6337 63.37%
Human Ether-a-go-go-Related Gene inhibition - 0.5492 54.92%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.6000 60.00%
skin sensitisation + 0.8476 84.76%
Respiratory toxicity - 0.5778 57.78%
Reproductive toxicity - 0.7667 76.67%
Mitochondrial toxicity - 0.6250 62.50%
Nephrotoxicity - 0.5855 58.55%
Acute Oral Toxicity (c) III 0.5750 57.50%
Estrogen receptor binding - 0.8302 83.02%
Androgen receptor binding - 0.9128 91.28%
Thyroid receptor binding - 0.7344 73.44%
Glucocorticoid receptor binding - 0.5933 59.33%
Aromatase binding - 0.7012 70.12%
PPAR gamma - 0.6477 64.77%
Honey bee toxicity - 0.9637 96.37%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.5900 59.00%
Fish aquatic toxicity + 0.9735 97.35%

Targets

Top

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 93.70% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.61% 91.11%
CHEMBL4208 P20618 Proteasome component C5 85.45% 90.00%
CHEMBL253 P34972 Cannabinoid CB2 receptor 85.02% 97.25%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.69% 95.56%
CHEMBL2581 P07339 Cathepsin D 83.85% 98.95%
CHEMBL2996 Q05655 Protein kinase C delta 80.23% 97.79%

Plants that contains it

Top
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.
Asteriscus intermedius

Cross-Links

Top
PubChem 85647490
LOTUS LTS0166579
wikiData Q105153595