(8-Acetyloxy-2,6-dimethylocta-2,6-dienyl) 2-methylbutanoate

Details

Top
Internal ID cbdd1e02-2ad8-42fa-99eb-54221b450cda
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohol esters
IUPAC Name (8-acetyloxy-2,6-dimethylocta-2,6-dienyl) 2-methylbutanoate
SMILES (Canonical) CCC(C)C(=O)OCC(=CCCC(=CCOC(=O)C)C)C
SMILES (Isomeric) CCC(C)C(=O)OCC(=CCCC(=CCOC(=O)C)C)C
InChI InChI=1S/C17H28O4/c1-6-15(4)17(19)21-12-14(3)9-7-8-13(2)10-11-20-16(5)18/h9-10,15H,6-8,11-12H2,1-5H3
InChI Key WEBJVWPPMGGELG-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C17H28O4
Molecular Weight 296.40 g/mol
Exact Mass 296.19875937 g/mol
Topological Polar Surface Area (TPSA) 52.60 Ų
XlogP 4.20
Atomic LogP (AlogP) 3.81
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 9

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of (8-Acetyloxy-2,6-dimethylocta-2,6-dienyl) 2-methylbutanoate

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9827 98.27%
Caco-2 + 0.8764 87.64%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.7024 70.24%
OATP2B1 inhibitior - 0.8520 85.20%
OATP1B1 inhibitior + 0.8828 88.28%
OATP1B3 inhibitior + 0.9422 94.22%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior + 0.7610 76.10%
P-glycoprotein inhibitior - 0.7198 71.98%
P-glycoprotein substrate - 0.8927 89.27%
CYP3A4 substrate - 0.5365 53.65%
CYP2C9 substrate + 0.5955 59.55%
CYP2D6 substrate - 0.8761 87.61%
CYP3A4 inhibition - 0.8702 87.02%
CYP2C9 inhibition - 0.8490 84.90%
CYP2C19 inhibition - 0.8224 82.24%
CYP2D6 inhibition - 0.8805 88.05%
CYP1A2 inhibition - 0.8054 80.54%
CYP2C8 inhibition - 0.8947 89.47%
CYP inhibitory promiscuity - 0.7143 71.43%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6423 64.23%
Carcinogenicity (trinary) Non-required 0.6173 61.73%
Eye corrosion - 0.7077 70.77%
Eye irritation - 0.6692 66.92%
Skin irritation + 0.5483 54.83%
Skin corrosion - 0.9850 98.50%
Ames mutagenesis - 0.6078 60.78%
Human Ether-a-go-go-Related Gene inhibition - 0.4365 43.65%
Micronuclear - 0.9600 96.00%
Hepatotoxicity + 0.5054 50.54%
skin sensitisation - 0.9233 92.33%
Respiratory toxicity - 0.8222 82.22%
Reproductive toxicity - 0.9812 98.12%
Mitochondrial toxicity - 0.9625 96.25%
Nephrotoxicity + 0.5770 57.70%
Acute Oral Toxicity (c) IV 0.7579 75.79%
Estrogen receptor binding - 0.8616 86.16%
Androgen receptor binding - 0.5904 59.04%
Thyroid receptor binding - 0.6171 61.71%
Glucocorticoid receptor binding - 0.5996 59.96%
Aromatase binding - 0.7569 75.69%
PPAR gamma - 0.7934 79.34%
Honey bee toxicity - 0.8513 85.13%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity - 0.6255 62.55%
Fish aquatic toxicity + 0.9968 99.68%

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 95.45% 96.09%
CHEMBL2581 P07339 Cathepsin D 93.34% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.22% 94.45%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.96% 99.17%
CHEMBL253 P34972 Cannabinoid CB2 receptor 85.58% 97.25%
CHEMBL3401 O75469 Pregnane X receptor 83.30% 94.73%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 82.60% 100.00%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 81.96% 89.34%
CHEMBL2413 P32246 C-C chemokine receptor type 1 81.67% 89.50%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 81.49% 92.08%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.43% 96.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.15% 91.11%

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.
Liatris cylindracea

Cross-Links

Top
PubChem 162970264
LOTUS LTS0095070
wikiData Q105302846