2,6,6,9-Tetramethyltricyclo[5.3.1.01,5]undecan-9-ol

Details

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Internal ID 14f4eeaf-068f-4793-9b67-4c217d515303
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Tertiary alcohols
IUPAC Name 2,6,6,9-tetramethyltricyclo[5.3.1.01,5]undecan-9-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H26O/c1-10-5-6-12-13(2,3)11-7-14(4,16)9-15(10,12)8-11/h10-12,16H,5-9H2,1-4H3
InChI Key PCROEXHGMUJCDB-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) 3.61
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2,6,6,9-Tetramethyltricyclo[5.3.1.01,5]undecan-9-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9941 99.41%
Caco-2 + 0.7800 78.00%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Lysosomes 0.6987 69.87%
OATP2B1 inhibitior - 0.8440 84.40%
OATP1B1 inhibitior + 0.9587 95.87%
OATP1B3 inhibitior + 0.9590 95.90%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9414 94.14%
P-glycoprotein inhibitior - 0.9447 94.47%
P-glycoprotein substrate - 0.8797 87.97%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate + 0.6165 61.65%
CYP2D6 substrate - 0.7496 74.96%
CYP3A4 inhibition - 0.9641 96.41%
CYP2C9 inhibition - 0.7296 72.96%
CYP2C19 inhibition - 0.8585 85.85%
CYP2D6 inhibition - 0.9623 96.23%
CYP1A2 inhibition - 0.6378 63.78%
CYP2C8 inhibition - 0.9021 90.21%
CYP inhibitory promiscuity - 0.9597 95.97%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8100 81.00%
Carcinogenicity (trinary) Non-required 0.6816 68.16%
Eye corrosion - 0.9061 90.61%
Eye irritation + 0.8233 82.33%
Skin irritation + 0.7749 77.49%
Skin corrosion - 0.8763 87.63%
Ames mutagenesis - 0.8037 80.37%
Human Ether-a-go-go-Related Gene inhibition - 0.5210 52.10%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.5750 57.50%
skin sensitisation + 0.6694 66.94%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity + 0.6556 65.56%
Mitochondrial toxicity + 0.5875 58.75%
Nephrotoxicity - 0.6013 60.13%
Acute Oral Toxicity (c) III 0.8523 85.23%
Estrogen receptor binding - 0.4746 47.46%
Androgen receptor binding - 0.5752 57.52%
Thyroid receptor binding - 0.6480 64.80%
Glucocorticoid receptor binding - 0.6671 66.71%
Aromatase binding + 0.5392 53.92%
PPAR gamma - 0.7727 77.27%
Honey bee toxicity - 0.8843 88.43%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.6100 61.00%
Fish aquatic toxicity + 0.8339 83.39%

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 90.69% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 89.35% 97.25%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 83.43% 96.38%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 82.76% 82.69%
CHEMBL241 Q14432 Phosphodiesterase 3A 82.10% 92.94%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.46% 91.11%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 80.82% 95.50%
CHEMBL3137262 O60341 LSD1/CoREST complex 80.48% 97.09%
CHEMBL206 P03372 Estrogen receptor alpha 80.39% 97.64%
CHEMBL259 P32245 Melanocortin receptor 4 80.11% 95.38%

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.
Juniperus cedrus

Cross-Links

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PubChem 162901818
LOTUS LTS0180084
wikiData Q105205943