(1,12-Dihydroxy-2,6,10-trimethyldodeca-2,6,10-trien-5-yl) acetate

Details

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Internal ID 1254fe76-1964-4ca5-9373-62c0ff639fd5
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (1,12-dihydroxy-2,6,10-trimethyldodeca-2,6,10-trien-5-yl) acetate
SMILES (Canonical) CC(=CCO)CCC=C(C)C(CC=C(C)CO)OC(=O)C
SMILES (Isomeric) CC(=CCO)CCC=C(C)C(CC=C(C)CO)OC(=O)C
InChI InChI=1S/C17H28O4/c1-13(10-11-18)6-5-7-15(3)17(21-16(4)20)9-8-14(2)12-19/h7-8,10,17-19H,5-6,9,11-12H2,1-4H3
InChI Key FKZKSYSFWQITBQ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C17H28O4
Molecular Weight 296.40 g/mol
Exact Mass 296.19875937 g/mol
Topological Polar Surface Area (TPSA) 66.80 Ų
XlogP 3.00
Atomic LogP (AlogP) 2.91
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 9

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (1,12-Dihydroxy-2,6,10-trimethyldodeca-2,6,10-trien-5-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 + 0.8994 89.94%
Caco-2 + 0.8462 84.62%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.7286 72.86%
Subcellular localzation Mitochondria 0.8026 80.26%
OATP2B1 inhibitior - 0.8552 85.52%
OATP1B1 inhibitior + 0.9382 93.82%
OATP1B3 inhibitior + 0.9248 92.48%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior + 0.8273 82.73%
P-glycoprotein inhibitior - 0.8006 80.06%
P-glycoprotein substrate - 0.9025 90.25%
CYP3A4 substrate + 0.5381 53.81%
CYP2C9 substrate - 0.8100 81.00%
CYP2D6 substrate - 0.8712 87.12%
CYP3A4 inhibition - 0.7596 75.96%
CYP2C9 inhibition - 0.8909 89.09%
CYP2C19 inhibition - 0.8759 87.59%
CYP2D6 inhibition - 0.8810 88.10%
CYP1A2 inhibition - 0.7946 79.46%
CYP2C8 inhibition - 0.8608 86.08%
CYP inhibitory promiscuity - 0.7970 79.70%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.7223 72.23%
Carcinogenicity (trinary) Non-required 0.7213 72.13%
Eye corrosion - 0.9174 91.74%
Eye irritation - 0.7815 78.15%
Skin irritation - 0.7733 77.33%
Skin corrosion - 0.9925 99.25%
Ames mutagenesis - 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7575 75.75%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.6843 68.43%
skin sensitisation - 0.7332 73.32%
Respiratory toxicity - 0.8333 83.33%
Reproductive toxicity - 0.9333 93.33%
Mitochondrial toxicity - 0.7250 72.50%
Nephrotoxicity + 0.5634 56.34%
Acute Oral Toxicity (c) III 0.5492 54.92%
Estrogen receptor binding - 0.5610 56.10%
Androgen receptor binding - 0.7576 75.76%
Thyroid receptor binding - 0.5811 58.11%
Glucocorticoid receptor binding - 0.5873 58.73%
Aromatase binding - 0.6284 62.84%
PPAR gamma + 0.7155 71.55%
Honey bee toxicity - 0.8502 85.02%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity - 0.6300 63.00%
Fish aquatic toxicity + 0.9179 91.79%

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 91.91% 96.09%
CHEMBL2581 P07339 Cathepsin D 90.78% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.26% 99.17%
CHEMBL340 P08684 Cytochrome P450 3A4 86.11% 91.19%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.05% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.51% 94.45%

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.
Ursinia anthemoides

Cross-Links

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PubChem 162943156
LOTUS LTS0216659
wikiData Q104996891