3,14-Diacetyloxytetradeca-4,6,12-trien-8,10-diynyl acetate

Details

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Internal ID f0741783-f322-4fb8-9fc7-4655a61d8232
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohol esters
IUPAC Name 3,14-diacetyloxytetradeca-4,6,12-trien-8,10-diynyl acetate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H22O6/c1-17(21)24-15-12-10-8-6-4-5-7-9-11-13-20(26-19(3)23)14-16-25-18(2)22/h7,9-13,20H,14-16H2,1-3H3
InChI Key FHMJPDDYIZJLRC-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H22O6
Molecular Weight 358.40 g/mol
Exact Mass 358.14163842 g/mol
Topological Polar Surface Area (TPSA) 78.90 Ų
XlogP 2.70
Atomic LogP (AlogP) 2.11
H-Bond Acceptor 6
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 3,14-Diacetyloxytetradeca-4,6,12-trien-8,10-diynyl acetate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9466 94.66%
Caco-2 - 0.6641 66.41%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability - 0.8000 80.00%
Subcellular localzation Mitochondria 0.8046 80.46%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8866 88.66%
OATP1B3 inhibitior + 0.9493 94.93%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.5442 54.42%
P-glycoprotein inhibitior - 0.4932 49.32%
P-glycoprotein substrate - 0.7962 79.62%
CYP3A4 substrate + 0.5878 58.78%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8720 87.20%
CYP3A4 inhibition - 0.6624 66.24%
CYP2C9 inhibition - 0.8556 85.56%
CYP2C19 inhibition - 0.8503 85.03%
CYP2D6 inhibition - 0.9295 92.95%
CYP1A2 inhibition - 0.8292 82.92%
CYP2C8 inhibition - 0.8296 82.96%
CYP inhibitory promiscuity - 0.7651 76.51%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5823 58.23%
Carcinogenicity (trinary) Non-required 0.6371 63.71%
Eye corrosion + 0.5530 55.30%
Eye irritation - 0.9464 94.64%
Skin irritation - 0.5265 52.65%
Skin corrosion - 0.9054 90.54%
Ames mutagenesis - 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3888 38.88%
Micronuclear - 0.9200 92.00%
Hepatotoxicity + 0.5461 54.61%
skin sensitisation - 0.7738 77.38%
Respiratory toxicity - 0.8111 81.11%
Reproductive toxicity - 0.9444 94.44%
Mitochondrial toxicity - 0.9000 90.00%
Nephrotoxicity + 0.8060 80.60%
Acute Oral Toxicity (c) III 0.7943 79.43%
Estrogen receptor binding + 0.8023 80.23%
Androgen receptor binding - 0.5321 53.21%
Thyroid receptor binding + 0.5171 51.71%
Glucocorticoid receptor binding + 0.6536 65.36%
Aromatase binding + 0.6301 63.01%
PPAR gamma + 0.6614 66.14%
Honey bee toxicity - 0.7201 72.01%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.7688 76.88%

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 94.77% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.15% 99.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.38% 94.45%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 85.32% 96.00%
CHEMBL253 P34972 Cannabinoid CB2 receptor 82.08% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.93% 91.11%
CHEMBL3145 P42338 PI3-kinase p110-beta subunit 80.79% 98.75%
CHEMBL2581 P07339 Cathepsin D 80.31% 98.95%

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 162873500
LOTUS LTS0025767
wikiData Q104995340