10-Acetyloxydeca-6,8-dien-4-ynyl acetate

Details

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Internal ID a0cb6783-b742-4402-9886-8f739a977b49
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohol esters
IUPAC Name 10-acetyloxydeca-6,8-dien-4-ynyl acetate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C14H18O4/c1-13(15)17-11-9-7-5-3-4-6-8-10-12-18-14(2)16/h3,5,7,9H,8,10-12H2,1-2H3
InChI Key UFQMJYKAVGPLDX-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C14H18O4
Molecular Weight 250.29 g/mol
Exact Mass 250.12050905 g/mol
Topological Polar Surface Area (TPSA) 52.60 Ų
XlogP 2.20
Atomic LogP (AlogP) 2.01
H-Bond Acceptor 4
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 10-Acetyloxydeca-6,8-dien-4-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 + 0.9479 94.79%
Caco-2 + 0.5706 57.06%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.7833 78.33%
OATP2B1 inhibitior - 0.8590 85.90%
OATP1B1 inhibitior + 0.8997 89.97%
OATP1B3 inhibitior + 0.9480 94.80%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.7679 76.79%
P-glycoprotein inhibitior - 0.9292 92.92%
P-glycoprotein substrate - 0.9220 92.20%
CYP3A4 substrate + 0.5345 53.45%
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 - 0.8519 85.19%
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 - 0.7306 73.06%
Skin irritation + 0.5956 59.56%
Skin corrosion - 0.8583 85.83%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6733 67.33%
Micronuclear - 0.9700 97.00%
Hepatotoxicity + 0.6250 62.50%
skin sensitisation + 0.4832 48.32%
Respiratory toxicity - 0.7889 78.89%
Reproductive toxicity - 0.9000 90.00%
Mitochondrial toxicity - 0.9500 95.00%
Nephrotoxicity + 0.8736 87.36%
Acute Oral Toxicity (c) III 0.6942 69.42%
Estrogen receptor binding - 0.6597 65.97%
Androgen receptor binding - 0.5735 57.35%
Thyroid receptor binding + 0.5323 53.23%
Glucocorticoid receptor binding - 0.6136 61.36%
Aromatase binding - 0.6094 60.94%
PPAR gamma - 0.6723 67.23%
Honey bee toxicity - 0.8522 85.22%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity + 0.5400 54.00%
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 95.66% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.34% 99.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.53% 91.11%
CHEMBL2581 P07339 Cathepsin D 81.35% 98.95%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.95% 96.00%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.03% 96.95%

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 162912581
LOTUS LTS0056319
wikiData Q105272030