methyl 2-(6-methoxy-6-tetradeca-10,12-dienyl-3H-1,2-dioxin-3-yl)acetate

Details

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Internal ID dc757172-9a2f-4400-942d-be89c0af47f8
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Carboxylic acid derivatives > Carboxylic acid esters > Methyl esters
IUPAC Name methyl 2-(6-methoxy-6-tetradeca-10,12-dienyl-3H-1,2-dioxin-3-yl)acetate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C22H36O5/c1-4-5-6-7-8-9-10-11-12-13-14-15-17-22(25-3)18-16-20(26-27-22)19-21(23)24-2/h4-7,16,18,20H,8-15,17,19H2,1-3H3
InChI Key HVYBFBDAGMLZEH-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C22H36O5
Molecular Weight 380.50 g/mol
Exact Mass 380.25627424 g/mol
Topological Polar Surface Area (TPSA) 54.00 Ų
XlogP 6.00
Atomic LogP (AlogP) 5.42
H-Bond Acceptor 5
H-Bond Donor 0
Rotatable Bonds 14

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of methyl 2-(6-methoxy-6-tetradeca-10,12-dienyl-3H-1,2-dioxin-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 + 0.8891 88.91%
Caco-2 - 0.5545 55.45%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.6606 66.06%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8255 82.55%
OATP1B3 inhibitior + 0.9163 91.63%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior + 0.9239 92.39%
P-glycoprotein inhibitior + 0.6876 68.76%
P-glycoprotein substrate - 0.5756 57.56%
CYP3A4 substrate + 0.6265 62.65%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8788 87.88%
CYP3A4 inhibition - 0.9501 95.01%
CYP2C9 inhibition - 0.9462 94.62%
CYP2C19 inhibition - 0.8563 85.63%
CYP2D6 inhibition - 0.9352 93.52%
CYP1A2 inhibition - 0.8433 84.33%
CYP2C8 inhibition + 0.4648 46.48%
CYP inhibitory promiscuity - 0.9346 93.46%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8728 87.28%
Carcinogenicity (trinary) Non-required 0.6895 68.95%
Eye corrosion - 0.9179 91.79%
Eye irritation - 0.8932 89.32%
Skin irritation - 0.7265 72.65%
Skin corrosion - 0.9704 97.04%
Ames mutagenesis - 0.5454 54.54%
Human Ether-a-go-go-Related Gene inhibition + 0.8936 89.36%
Micronuclear - 0.8500 85.00%
Hepatotoxicity - 0.5966 59.66%
skin sensitisation - 0.8156 81.56%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity - 0.7556 75.56%
Mitochondrial toxicity - 0.7500 75.00%
Nephrotoxicity + 0.6130 61.30%
Acute Oral Toxicity (c) III 0.5806 58.06%
Estrogen receptor binding + 0.8631 86.31%
Androgen receptor binding + 0.6113 61.13%
Thyroid receptor binding + 0.6050 60.50%
Glucocorticoid receptor binding + 0.7407 74.07%
Aromatase binding + 0.5858 58.58%
PPAR gamma - 0.4907 49.07%
Honey bee toxicity - 0.8470 84.70%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity + 0.6637 66.37%
Fish aquatic toxicity + 0.7204 72.04%

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 96.72% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.34% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 93.99% 99.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.63% 94.45%
CHEMBL3401 O75469 Pregnane X receptor 85.45% 94.73%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 83.55% 94.33%
CHEMBL4227 P25090 Lipoxin A4 receptor 82.08% 100.00%
CHEMBL2179 P04062 Beta-glucocerebrosidase 80.31% 85.31%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 556855
LOTUS LTS0248706
wikiData Q105034494