14-Acetyloxytetradeca-4,6,12-trien-8,10-diynyl acetate

Details

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Internal ID 62f463bb-2c07-4eb3-9a80-016e9f099be7
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohol esters
IUPAC Name 14-acetyloxytetradeca-4,6,12-trien-8,10-diynyl acetate
SMILES (Canonical) CC(=O)OCCCC=CC=CC#CC#CC=CCOC(=O)C
SMILES (Isomeric) CC(=O)OCCCC=CC=CC#CC#CC=CCOC(=O)C
InChI InChI=1S/C18H20O4/c1-17(19)21-15-13-11-9-7-5-3-4-6-8-10-12-14-16-22-18(2)20/h3,5,7,9,12,14H,11,13,15-16H2,1-2H3
InChI Key QHXFTVWYKDZXPJ-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C18H20O4
Molecular Weight 300.30 g/mol
Exact Mass 300.13615911 g/mol
Topological Polar Surface Area (TPSA) 52.60 Ų
XlogP 3.20
Atomic LogP (AlogP) 2.57
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 14-Acetyloxytetradeca-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 + 0.9479 94.79%
Caco-2 - 0.5517 55.17%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.7833 78.33%
OATP2B1 inhibitior - 0.8586 85.86%
OATP1B1 inhibitior + 0.8868 88.68%
OATP1B3 inhibitior + 0.9480 94.80%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.5799 57.99%
P-glycoprotein inhibitior - 0.7529 75.29%
P-glycoprotein substrate - 0.8986 89.86%
CYP3A4 substrate + 0.5722 57.22%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8720 87.20%
CYP3A4 inhibition - 0.8169 81.69%
CYP2C9 inhibition - 0.8968 89.68%
CYP2C19 inhibition - 0.9112 91.12%
CYP2D6 inhibition - 0.9308 93.08%
CYP1A2 inhibition - 0.8189 81.89%
CYP2C8 inhibition - 0.8635 86.35%
CYP inhibitory promiscuity - 0.8330 83.30%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6323 63.23%
Carcinogenicity (trinary) Non-required 0.7064 70.64%
Eye corrosion + 0.8291 82.91%
Eye irritation - 0.9077 90.77%
Skin irritation + 0.5956 59.56%
Skin corrosion - 0.8583 85.83%
Ames mutagenesis - 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4469 44.69%
Micronuclear - 0.9700 97.00%
Hepatotoxicity + 0.6125 61.25%
skin sensitisation + 0.4832 48.32%
Respiratory toxicity - 0.7778 77.78%
Reproductive toxicity - 0.9000 90.00%
Mitochondrial toxicity - 0.9500 95.00%
Nephrotoxicity + 0.8963 89.63%
Acute Oral Toxicity (c) III 0.6942 69.42%
Estrogen receptor binding + 0.5867 58.67%
Androgen receptor binding + 0.5469 54.69%
Thyroid receptor binding - 0.5076 50.76%
Glucocorticoid receptor binding + 0.5674 56.74%
Aromatase binding + 0.5628 56.28%
PPAR gamma + 0.6602 66.02%
Honey bee toxicity - 0.8452 84.52%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.5500 55.00%
Fish aquatic toxicity + 0.8831 88.31%

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 94.33% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.29% 99.17%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 85.25% 96.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.82% 94.45%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.07% 96.00%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 81.24% 97.21%

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 163039787
LOTUS LTS0172746
wikiData Q105022533