(10-Hydroxy-2,6,10-trimethyldodeca-2,6,11-trien-5-yl) acetate

Details

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Internal ID fa9280ed-caf8-480f-bcef-250888b0cc1b
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (10-hydroxy-2,6,10-trimethyldodeca-2,6,11-trien-5-yl) acetate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H28O3/c1-7-17(6,19)12-8-9-14(4)16(20-15(5)18)11-10-13(2)3/h7,9-10,16,19H,1,8,11-12H2,2-6H3
InChI Key INVDOMGOTJDZEO-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C17H28O3
Molecular Weight 280.40 g/mol
Exact Mass 280.20384475 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 4.00
Atomic LogP (AlogP) 3.94
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 8

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (10-Hydroxy-2,6,10-trimethyldodeca-2,6,11-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 + 0.9906 99.06%
Caco-2 + 0.7934 79.34%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability - 0.7000 70.00%
Subcellular localzation Mitochondria 0.7124 71.24%
OATP2B1 inhibitior - 0.8550 85.50%
OATP1B1 inhibitior + 0.9314 93.14%
OATP1B3 inhibitior + 0.9314 93.14%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior + 0.7007 70.07%
P-glycoprotein inhibitior - 0.8380 83.80%
P-glycoprotein substrate - 0.9153 91.53%
CYP3A4 substrate + 0.5576 55.76%
CYP2C9 substrate - 0.8032 80.32%
CYP2D6 substrate - 0.8754 87.54%
CYP3A4 inhibition - 0.8100 81.00%
CYP2C9 inhibition - 0.7615 76.15%
CYP2C19 inhibition - 0.8382 83.82%
CYP2D6 inhibition - 0.9433 94.33%
CYP1A2 inhibition - 0.7934 79.34%
CYP2C8 inhibition - 0.8048 80.48%
CYP inhibitory promiscuity - 0.9156 91.56%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.5915 59.15%
Carcinogenicity (trinary) Non-required 0.6298 62.98%
Eye corrosion - 0.8035 80.35%
Eye irritation - 0.7723 77.23%
Skin irritation + 0.7262 72.62%
Skin corrosion - 0.9450 94.50%
Ames mutagenesis - 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6812 68.12%
Micronuclear - 0.9600 96.00%
Hepatotoxicity - 0.5659 56.59%
skin sensitisation + 0.7914 79.14%
Respiratory toxicity - 0.8222 82.22%
Reproductive toxicity - 0.8087 80.87%
Mitochondrial toxicity - 0.8125 81.25%
Nephrotoxicity + 0.5590 55.90%
Acute Oral Toxicity (c) III 0.6783 67.83%
Estrogen receptor binding - 0.5692 56.92%
Androgen receptor binding - 0.8109 81.09%
Thyroid receptor binding - 0.5387 53.87%
Glucocorticoid receptor binding + 0.5433 54.33%
Aromatase binding - 0.5893 58.93%
PPAR gamma + 0.7657 76.57%
Honey bee toxicity - 0.7022 70.22%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.7700 77.00%
Fish aquatic toxicity + 0.9541 95.41%

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
CHEMBL2581 P07339 Cathepsin D 91.42% 98.95%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 90.38% 97.21%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 89.52% 96.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.69% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 87.44% 94.73%
CHEMBL5966 P55899 IgG receptor FcRn large subunit p51 85.74% 90.93%
CHEMBL4005 P42336 PI3-kinase p110-alpha subunit 84.14% 97.47%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.78% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.12% 94.45%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 80.88% 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.
Ursinia dentata

Cross-Links

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PubChem 162919075
LOTUS LTS0198937
wikiData Q105116426