Tetradeca-4,6,10,12-tetraen-8-ynyl acetate

Details

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Internal ID d24721a4-db43-4477-83b0-fc0f3cb1650a
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohol esters
IUPAC Name tetradeca-4,6,10,12-tetraen-8-ynyl acetate
SMILES (Canonical) CC=CC=CC#CC=CC=CCCCOC(=O)C
SMILES (Isomeric) CC=CC=CC#CC=CC=CCCCOC(=O)C
InChI InChI=1S/C16H20O2/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-18-16(2)17/h3-6,9-12H,13-15H2,1-2H3
InChI Key UWBOXJNXDPRYIO-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C16H20O2
Molecular Weight 244.33 g/mol
Exact Mass 244.146329876 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 4.10
Atomic LogP (AlogP) 3.58
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Tetradeca-4,6,10,12-tetraen-8-ynyl acetate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9942 99.42%
Caco-2 + 0.7397 73.97%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Mitochondria 0.6283 62.83%
OATP2B1 inhibitior - 0.8610 86.10%
OATP1B1 inhibitior + 0.8730 87.30%
OATP1B3 inhibitior + 0.9250 92.50%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.6786 67.86%
P-glycoprotein inhibitior - 0.8938 89.38%
P-glycoprotein substrate - 0.9332 93.32%
CYP3A4 substrate + 0.5439 54.39%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8720 87.20%
CYP3A4 inhibition - 0.8954 89.54%
CYP2C9 inhibition - 0.9402 94.02%
CYP2C19 inhibition - 0.9319 93.19%
CYP2D6 inhibition - 0.9502 95.02%
CYP1A2 inhibition - 0.5774 57.74%
CYP2C8 inhibition - 0.8826 88.26%
CYP inhibitory promiscuity - 0.7772 77.72%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5900 59.00%
Carcinogenicity (trinary) Non-required 0.6698 66.98%
Eye corrosion + 0.9648 96.48%
Eye irritation - 0.8451 84.51%
Skin irritation + 0.8561 85.61%
Skin corrosion - 0.8775 87.75%
Ames mutagenesis - 0.8100 81.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6757 67.57%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.5250 52.50%
skin sensitisation + 0.7342 73.42%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity - 0.9556 95.56%
Mitochondrial toxicity - 0.9875 98.75%
Nephrotoxicity + 0.8498 84.98%
Acute Oral Toxicity (c) III 0.7418 74.18%
Estrogen receptor binding + 0.5477 54.77%
Androgen receptor binding - 0.5282 52.82%
Thyroid receptor binding - 0.5053 50.53%
Glucocorticoid receptor binding + 0.5890 58.90%
Aromatase binding + 0.5937 59.37%
PPAR gamma + 0.5371 53.71%
Honey bee toxicity - 0.8661 86.61%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity + 0.5400 54.00%
Fish aquatic toxicity + 0.7243 72.43%

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 93.60% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.29% 99.17%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 85.75% 96.95%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 84.61% 97.21%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.94% 94.45%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 81.64% 94.33%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.53% 96.00%
CHEMBL2581 P07339 Cathepsin D 80.64% 98.95%

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.
Centaurea cineraria subsp. cineraria
Cotula coronopifolia
Saussurea alpina

Cross-Links

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PubChem 162868798
LOTUS LTS0062090
wikiData Q105280263