(3,7,11-Trimethyl-8-oxododeca-1,6,10-trien-3-yl) acetate

Details

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Internal ID 3ce2e279-9577-4288-a180-39ff628a0a75
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (3,7,11-trimethyl-8-oxododeca-1,6,10-trien-3-yl) acetate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H26O3/c1-7-17(6,20-15(5)18)12-8-9-14(4)16(19)11-10-13(2)3/h7,9-10H,1,8,11-12H2,2-6H3
InChI Key GZQFUVVJSNQSHL-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C17H26O3
Molecular Weight 278.40 g/mol
Exact Mass 278.18819469 g/mol
Topological Polar Surface Area (TPSA) 43.40 Ų
XlogP 3.80
Atomic LogP (AlogP) 4.15
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 8

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (3,7,11-Trimethyl-8-oxododeca-1,6,10-trien-3-yl) acetate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9862 98.62%
Caco-2 + 0.6277 62.77%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.7252 72.52%
OATP2B1 inhibitior - 0.8565 85.65%
OATP1B1 inhibitior + 0.9140 91.40%
OATP1B3 inhibitior + 0.8640 86.40%
MATE1 inhibitior - 0.5600 56.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.5000 50.00%
P-glycoprotein inhibitior - 0.8412 84.12%
P-glycoprotein substrate - 0.9195 91.95%
CYP3A4 substrate + 0.5151 51.51%
CYP2C9 substrate - 0.7759 77.59%
CYP2D6 substrate - 0.9001 90.01%
CYP3A4 inhibition - 0.7998 79.98%
CYP2C9 inhibition - 0.7850 78.50%
CYP2C19 inhibition - 0.7460 74.60%
CYP2D6 inhibition - 0.9420 94.20%
CYP1A2 inhibition - 0.7696 76.96%
CYP2C8 inhibition - 0.9165 91.65%
CYP inhibitory promiscuity - 0.8371 83.71%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5123 51.23%
Carcinogenicity (trinary) Non-required 0.5363 53.63%
Eye corrosion - 0.6506 65.06%
Eye irritation + 0.7980 79.80%
Skin irritation + 0.7138 71.38%
Skin corrosion - 0.9826 98.26%
Ames mutagenesis - 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3890 38.90%
Micronuclear - 0.9200 92.00%
Hepatotoxicity + 0.5544 55.44%
skin sensitisation + 0.8185 81.85%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity - 0.9222 92.22%
Mitochondrial toxicity - 0.8625 86.25%
Nephrotoxicity + 0.6712 67.12%
Acute Oral Toxicity (c) III 0.6360 63.60%
Estrogen receptor binding - 0.6595 65.95%
Androgen receptor binding - 0.8113 81.13%
Thyroid receptor binding - 0.5902 59.02%
Glucocorticoid receptor binding - 0.7490 74.90%
Aromatase binding - 0.6774 67.74%
PPAR gamma + 0.5637 56.37%
Honey bee toxicity - 0.6858 68.58%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity + 0.9828 98.28%

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 90.36% 96.09%
CHEMBL2581 P07339 Cathepsin D 89.56% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.97% 91.11%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 87.94% 91.24%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.69% 94.45%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.35% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 86.11% 94.73%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 85.35% 96.95%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 84.91% 89.34%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 83.17% 91.07%

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.
Artemisia gmelinii

Cross-Links

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PubChem 85531976
LOTUS LTS0106427
wikiData Q105024519