2,6,11,15-Tetramethylhexadeca-2,10,14-trien-6-ol

Details

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Internal ID 8b776e37-b66a-4efd-a3d4-44b265ca3fd4
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Acyclic diterpenoids
IUPAC Name 2,6,11,15-tetramethylhexadeca-2,10,14-trien-6-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H36O/c1-17(2)11-9-14-19(5)13-7-8-15-20(6,21)16-10-12-18(3)4/h11-13,21H,7-10,14-16H2,1-6H3
InChI Key CCCXGQLQJHWTLZ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H36O
Molecular Weight 292.50 g/mol
Exact Mass 292.276615768 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 6.60
Atomic LogP (AlogP) 6.35
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 10

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2,6,11,15-Tetramethylhexadeca-2,10,14-trien-6-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9891 98.91%
Caco-2 + 0.8399 83.99%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Lysosomes 0.3611 36.11%
OATP2B1 inhibitior - 0.8530 85.30%
OATP1B1 inhibitior + 0.9216 92.16%
OATP1B3 inhibitior + 0.9609 96.09%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.8809 88.09%
P-glycoprotein inhibitior - 0.8511 85.11%
P-glycoprotein substrate - 0.8952 89.52%
CYP3A4 substrate - 0.5431 54.31%
CYP2C9 substrate - 0.7899 78.99%
CYP2D6 substrate - 0.7511 75.11%
CYP3A4 inhibition - 0.9100 91.00%
CYP2C9 inhibition - 0.7941 79.41%
CYP2C19 inhibition - 0.8107 81.07%
CYP2D6 inhibition - 0.9470 94.70%
CYP1A2 inhibition - 0.6520 65.20%
CYP2C8 inhibition - 0.8976 89.76%
CYP inhibitory promiscuity - 0.7646 76.46%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.6700 67.00%
Carcinogenicity (trinary) Non-required 0.6452 64.52%
Eye corrosion - 0.8146 81.46%
Eye irritation - 0.5346 53.46%
Skin irritation + 0.7659 76.59%
Skin corrosion - 0.9749 97.49%
Ames mutagenesis - 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4348 43.48%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.7924 79.24%
skin sensitisation + 0.8780 87.80%
Respiratory toxicity - 0.8667 86.67%
Reproductive toxicity - 0.8053 80.53%
Mitochondrial toxicity - 0.8500 85.00%
Nephrotoxicity + 0.4849 48.49%
Acute Oral Toxicity (c) III 0.7571 75.71%
Estrogen receptor binding + 0.5425 54.25%
Androgen receptor binding - 0.7899 78.99%
Thyroid receptor binding + 0.5623 56.23%
Glucocorticoid receptor binding - 0.6719 67.19%
Aromatase binding - 0.7169 71.69%
PPAR gamma + 0.6019 60.19%
Honey bee toxicity - 0.9205 92.05%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity + 0.8940 89.40%

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
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 96.05% 92.08%
CHEMBL2581 P07339 Cathepsin D 89.32% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.50% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.24% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.75% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 86.27% 94.73%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 82.97% 96.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 80.53% 97.25%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 162980235
LOTUS LTS0015782
wikiData Q104953124