Pentadeca-5,7,13-trien-9,11-diynyl acetate

Details

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Internal ID 12ba9afe-4f39-45c1-ace7-a0949eb812e9
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohol esters
IUPAC Name pentadeca-5,7,13-trien-9,11-diynyl acetate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H20O2/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-19-17(2)18/h3-4,9-12H,13-16H2,1-2H3
InChI Key BKABLXPQLXVJQL-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C17H20O2
Molecular Weight 256.34 g/mol
Exact Mass 256.146329876 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 4.20
Atomic LogP (AlogP) 3.42
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 Pentadeca-5,7,13-trien-9,11-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 + 0.9937 99.37%
Caco-2 + 0.6817 68.17%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.6214 62.14%
OATP2B1 inhibitior - 0.8582 85.82%
OATP1B1 inhibitior + 0.8557 85.57%
OATP1B3 inhibitior + 0.9251 92.51%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.6878 68.78%
P-glycoprotein inhibitior - 0.8819 88.19%
P-glycoprotein substrate - 0.8983 89.83%
CYP3A4 substrate + 0.5372 53.72%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8720 87.20%
CYP3A4 inhibition - 0.8759 87.59%
CYP2C9 inhibition - 0.9267 92.67%
CYP2C19 inhibition - 0.9310 93.10%
CYP2D6 inhibition - 0.9413 94.13%
CYP1A2 inhibition - 0.5232 52.32%
CYP2C8 inhibition - 0.8287 82.87%
CYP inhibitory promiscuity - 0.7218 72.18%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6200 62.00%
Carcinogenicity (trinary) Non-required 0.6576 65.76%
Eye corrosion + 0.9566 95.66%
Eye irritation - 0.8400 84.00%
Skin irritation + 0.7871 78.71%
Skin corrosion - 0.9716 97.16%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7276 72.76%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.5500 55.00%
skin sensitisation + 0.8049 80.49%
Respiratory toxicity - 0.7556 75.56%
Reproductive toxicity - 0.9397 93.97%
Mitochondrial toxicity - 0.9875 98.75%
Nephrotoxicity + 0.7949 79.49%
Acute Oral Toxicity (c) III 0.8550 85.50%
Estrogen receptor binding - 0.4930 49.30%
Androgen receptor binding + 0.5672 56.72%
Thyroid receptor binding - 0.5206 52.06%
Glucocorticoid receptor binding - 0.4854 48.54%
Aromatase binding + 0.5220 52.20%
PPAR gamma - 0.4847 48.47%
Honey bee toxicity - 0.8763 87.63%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity + 0.6000 60.00%
Fish aquatic toxicity + 0.8838 88.38%

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
CHEMBL3060 Q9Y345 Glycine transporter 2 94.13% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.07% 96.09%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 86.09% 96.95%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 85.67% 97.21%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.41% 94.45%
CHEMBL2581 P07339 Cathepsin D 85.34% 98.95%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.37% 96.00%

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 162925509
LOTUS LTS0047108
wikiData Q104937460