1,4,4-Trimethyltricyclo[5.3.1.02,6]undecan-11-ol

Details

Top
Internal ID d21ff759-27a6-455f-985b-6986cb982279
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Cyclic alcohols and derivatives
IUPAC Name 1,4,4-trimethyltricyclo[5.3.1.02,6]undecan-11-ol
SMILES (Canonical) CC1(CC2C3CCCC(C2C1)(C3O)C)C
SMILES (Isomeric) CC1(CC2C3CCCC(C2C1)(C3O)C)C
InChI InChI=1S/C14H24O/c1-13(2)7-10-9-5-4-6-14(3,12(9)15)11(10)8-13/h9-12,15H,4-8H2,1-3H3
InChI Key GKUUOBPAWXVPEB-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C14H24O
Molecular Weight 208.34 g/mol
Exact Mass 208.182715385 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 3.90
Atomic LogP (AlogP) 3.22
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 1,4,4-Trimethyltricyclo[5.3.1.02,6]undecan-11-ol

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9937 99.37%
Caco-2 + 0.7290 72.90%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Lysosomes 0.5633 56.33%
OATP2B1 inhibitior - 0.8461 84.61%
OATP1B1 inhibitior + 0.9492 94.92%
OATP1B3 inhibitior + 0.9346 93.46%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.9309 93.09%
P-glycoprotein inhibitior - 0.9403 94.03%
P-glycoprotein substrate - 0.9528 95.28%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 0.5774 57.74%
CYP2D6 substrate - 0.6695 66.95%
CYP3A4 inhibition - 0.8893 88.93%
CYP2C9 inhibition - 0.6703 67.03%
CYP2C19 inhibition - 0.8399 83.99%
CYP2D6 inhibition - 0.9560 95.60%
CYP1A2 inhibition - 0.5268 52.68%
CYP2C8 inhibition - 0.9233 92.33%
CYP inhibitory promiscuity - 0.9098 90.98%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8600 86.00%
Carcinogenicity (trinary) Non-required 0.6521 65.21%
Eye corrosion - 0.9088 90.88%
Eye irritation + 0.9005 90.05%
Skin irritation + 0.6842 68.42%
Skin corrosion - 0.8744 87.44%
Ames mutagenesis - 0.8964 89.64%
Human Ether-a-go-go-Related Gene inhibition - 0.5127 51.27%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.5788 57.88%
skin sensitisation + 0.6535 65.35%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.5889 58.89%
Mitochondrial toxicity + 0.5375 53.75%
Nephrotoxicity - 0.6074 60.74%
Acute Oral Toxicity (c) III 0.7685 76.85%
Estrogen receptor binding - 0.6850 68.50%
Androgen receptor binding + 0.5676 56.76%
Thyroid receptor binding - 0.5058 50.58%
Glucocorticoid receptor binding - 0.6890 68.90%
Aromatase binding - 0.7282 72.82%
PPAR gamma - 0.8301 83.01%
Honey bee toxicity - 0.9479 94.79%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity + 0.6200 62.00%
Fish aquatic toxicity + 0.9767 97.67%

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 94.88% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 94.62% 97.25%
CHEMBL6136 O60341 Lysine-specific histone demethylase 1 92.37% 95.58%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.15% 97.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 89.15% 100.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.05% 91.11%
CHEMBL221 P23219 Cyclooxygenase-1 86.98% 90.17%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.55% 95.89%
CHEMBL1871 P10275 Androgen Receptor 81.91% 96.43%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 80.87% 93.04%
CHEMBL259 P32245 Melanocortin receptor 4 80.22% 95.38%

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.
Eugenia dysenterica
Hypericum hyssopifolium
Hyptis suaveolens

Cross-Links

Top
PubChem 529438
LOTUS LTS0148379
wikiData Q105010362