[(2E,5E)-7-hydroxy-3,7-dimethylocta-2,5-dienyl] acetate

Details

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Internal ID 44fe95b8-c355-4c94-990a-26952c9f1ee5
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohol esters
IUPAC Name [(2E,5E)-7-hydroxy-3,7-dimethylocta-2,5-dienyl] acetate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C12H20O3/c1-10(7-9-15-11(2)13)6-5-8-12(3,4)14/h5,7-8,14H,6,9H2,1-4H3/b8-5+,10-7+
InChI Key GPNYMDBKVQUQRW-FQOLVZPASA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C12H20O3
Molecular Weight 212.28 g/mol
Exact Mass 212.14124450 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 1.90
Atomic LogP (AlogP) 2.21
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [(2E,5E)-7-hydroxy-3,7-dimethylocta-2,5-dienyl] acetate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9791 97.91%
Caco-2 + 0.8877 88.77%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.8238 82.38%
OATP2B1 inhibitior - 0.8592 85.92%
OATP1B1 inhibitior + 0.9007 90.07%
OATP1B3 inhibitior + 0.9256 92.56%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.5519 55.19%
P-glycoprotein inhibitior - 0.9662 96.62%
P-glycoprotein substrate - 0.9656 96.56%
CYP3A4 substrate - 0.5228 52.28%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8757 87.57%
CYP3A4 inhibition - 0.8591 85.91%
CYP2C9 inhibition - 0.7487 74.87%
CYP2C19 inhibition - 0.8142 81.42%
CYP2D6 inhibition - 0.9148 91.48%
CYP1A2 inhibition - 0.8072 80.72%
CYP2C8 inhibition - 0.9090 90.90%
CYP inhibitory promiscuity - 0.6698 66.98%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.6140 61.40%
Carcinogenicity (trinary) Non-required 0.5318 53.18%
Eye corrosion - 0.7267 72.67%
Eye irritation + 0.9188 91.88%
Skin irritation + 0.6179 61.79%
Skin corrosion - 0.9724 97.24%
Ames mutagenesis + 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6294 62.94%
Micronuclear - 0.9300 93.00%
Hepatotoxicity + 0.5500 55.00%
skin sensitisation + 0.7563 75.63%
Respiratory toxicity - 0.8333 83.33%
Reproductive toxicity - 0.8556 85.56%
Mitochondrial toxicity - 0.7250 72.50%
Nephrotoxicity + 0.6909 69.09%
Acute Oral Toxicity (c) III 0.6096 60.96%
Estrogen receptor binding - 0.8850 88.50%
Androgen receptor binding - 0.9246 92.46%
Thyroid receptor binding - 0.8284 82.84%
Glucocorticoid receptor binding - 0.7384 73.84%
Aromatase binding - 0.8242 82.42%
PPAR gamma - 0.8519 85.19%
Honey bee toxicity - 0.8829 88.29%
Biodegradation + 0.6000 60.00%
Crustacea aquatic toxicity - 0.7800 78.00%
Fish aquatic toxicity + 0.9783 97.83%

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 90.06% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 88.31% 94.73%
CHEMBL253 P34972 Cannabinoid CB2 receptor 87.64% 97.25%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.98% 99.17%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 84.92% 89.34%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 84.77% 96.95%

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.
Chiliadenus montanus
Cyrtophyllum fragrans
Dovyalis abyssinica
Eucalyptus cordata
Nephelium ramboutan-ake

Cross-Links

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PubChem 14191351
NPASS NPC38213
LOTUS LTS0271243
wikiData Q105015024