2,6,6-Trimethylocta-2,7-dien-1-ol

Details

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Internal ID 5673247d-a4dd-49e9-8747-e695847833ea
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Acyclic monoterpenoids
IUPAC Name 2,6,6-trimethylocta-2,7-dien-1-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C11H20O/c1-5-11(3,4)8-6-7-10(2)9-12/h5,7,12H,1,6,8-9H2,2-4H3
InChI Key ALIHFCACWSVBTR-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C11H20O
Molecular Weight 168.28 g/mol
Exact Mass 168.151415257 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 3.50
Atomic LogP (AlogP) 2.92
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2,6,6-Trimethylocta-2,7-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 + 0.9719 97.19%
Caco-2 + 0.8744 87.44%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.7143 71.43%
Subcellular localzation Lysosomes 0.7199 71.99%
OATP2B1 inhibitior - 0.8545 85.45%
OATP1B1 inhibitior + 0.9416 94.16%
OATP1B3 inhibitior + 0.9092 90.92%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.7875 78.75%
P-glycoprotein inhibitior - 0.9828 98.28%
P-glycoprotein substrate - 0.9380 93.80%
CYP3A4 substrate - 0.5915 59.15%
CYP2C9 substrate - 0.8218 82.18%
CYP2D6 substrate - 0.7703 77.03%
CYP3A4 inhibition - 0.8356 83.56%
CYP2C9 inhibition - 0.8336 83.36%
CYP2C19 inhibition - 0.8468 84.68%
CYP2D6 inhibition - 0.9245 92.45%
CYP1A2 inhibition - 0.8843 88.43%
CYP2C8 inhibition - 0.9512 95.12%
CYP inhibitory promiscuity - 0.7752 77.52%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.6500 65.00%
Carcinogenicity (trinary) Non-required 0.6454 64.54%
Eye corrosion - 0.5815 58.15%
Eye irritation + 0.9489 94.89%
Skin irritation + 0.7946 79.46%
Skin corrosion - 0.9570 95.70%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6488 64.88%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.5873 58.73%
skin sensitisation + 0.8468 84.68%
Respiratory toxicity - 0.6778 67.78%
Reproductive toxicity - 0.9444 94.44%
Mitochondrial toxicity - 0.7250 72.50%
Nephrotoxicity + 0.6460 64.60%
Acute Oral Toxicity (c) III 0.8396 83.96%
Estrogen receptor binding - 0.9535 95.35%
Androgen receptor binding - 0.8377 83.77%
Thyroid receptor binding - 0.8894 88.94%
Glucocorticoid receptor binding - 0.7261 72.61%
Aromatase binding - 0.8861 88.61%
PPAR gamma - 0.8155 81.55%
Honey bee toxicity - 0.8170 81.70%
Biodegradation + 0.7750 77.50%
Crustacea aquatic toxicity - 0.6400 64.00%
Fish aquatic toxicity + 0.9756 97.56%

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
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 89.28% 89.34%
CHEMBL2581 P07339 Cathepsin D 87.95% 98.95%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 83.67% 97.29%
CHEMBL253 P34972 Cannabinoid CB2 receptor 82.47% 97.25%
CHEMBL3401 O75469 Pregnane X receptor 80.91% 94.73%

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.
Tectona grandis

Cross-Links

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PubChem 163046637
LOTUS LTS0012180
wikiData Q104914147