(3E,5E,7R,10E)-7-ethoxy-3,7,11,15-tetramethylhexadeca-1,3,5,10,14-pentaene

Details

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Internal ID 22516e64-2d88-4c7e-952e-1b43ebd59b42
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (3E,5E,7R,10E)-7-ethoxy-3,7,11,15-tetramethylhexadeca-1,3,5,10,14-pentaene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C22H36O/c1-8-20(5)15-11-17-22(7,23-9-2)18-12-16-21(6)14-10-13-19(3)4/h8,11,13,15-17H,1,9-10,12,14,18H2,2-7H3/b17-11+,20-15+,21-16+/t22-/m0/s1
InChI Key WVIIOGQLYAWFLP-SPQKUPAHSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C22H36O
Molecular Weight 316.50 g/mol
Exact Mass 316.276615768 g/mol
Topological Polar Surface Area (TPSA) 9.20 Ų
XlogP 7.40
Atomic LogP (AlogP) 6.94
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 11

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (3E,5E,7R,10E)-7-ethoxy-3,7,11,15-tetramethylhexadeca-1,3,5,10,14-pentaene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9929 99.29%
Caco-2 + 0.8174 81.74%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.4272 42.72%
OATP2B1 inhibitior - 0.8578 85.78%
OATP1B1 inhibitior + 0.9020 90.20%
OATP1B3 inhibitior + 0.9360 93.60%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior + 0.8535 85.35%
P-glycoprotein inhibitior - 0.5225 52.25%
P-glycoprotein substrate - 0.8300 83.00%
CYP3A4 substrate + 0.5868 58.68%
CYP2C9 substrate - 0.8032 80.32%
CYP2D6 substrate - 0.7504 75.04%
CYP3A4 inhibition - 0.8678 86.78%
CYP2C9 inhibition - 0.8402 84.02%
CYP2C19 inhibition - 0.7838 78.38%
CYP2D6 inhibition - 0.9218 92.18%
CYP1A2 inhibition - 0.6656 66.56%
CYP2C8 inhibition - 0.7625 76.25%
CYP inhibitory promiscuity - 0.5610 56.10%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5800 58.00%
Carcinogenicity (trinary) Non-required 0.4845 48.45%
Eye corrosion - 0.6934 69.34%
Eye irritation - 0.6183 61.83%
Skin irritation - 0.5173 51.73%
Skin corrosion - 0.9920 99.20%
Ames mutagenesis - 0.8100 81.00%
Human Ether-a-go-go-Related Gene inhibition + 0.9230 92.30%
Micronuclear - 0.9700 97.00%
Hepatotoxicity - 0.5625 56.25%
skin sensitisation + 0.7953 79.53%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity - 0.9889 98.89%
Mitochondrial toxicity - 0.8625 86.25%
Nephrotoxicity + 0.6479 64.79%
Acute Oral Toxicity (c) III 0.9015 90.15%
Estrogen receptor binding - 0.6015 60.15%
Androgen receptor binding - 0.8211 82.11%
Thyroid receptor binding + 0.6760 67.60%
Glucocorticoid receptor binding - 0.5649 56.49%
Aromatase binding + 0.5599 55.99%
PPAR gamma + 0.7793 77.93%
Honey bee toxicity - 0.6764 67.64%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.5800 58.00%
Fish aquatic toxicity + 0.9741 97.41%

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 93.65% 92.08%
CHEMBL2581 P07339 Cathepsin D 92.47% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.25% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 88.21% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.12% 99.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.52% 94.45%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 81.34% 89.34%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 80.88% 97.21%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.71% 96.95%

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 163002078
LOTUS LTS0019928
wikiData Q105313538