Heptadeca-1,9,16-trien-4,6-diyn-3-yl acetate

Details

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Internal ID 43d4b8c1-cce6-4f8b-a384-cc8d3ec8f01d
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohol esters
IUPAC Name heptadeca-1,9,16-trien-4,6-diyn-3-yl acetate
SMILES (Canonical) CC(=O)OC(C=C)C#CC#CCC=CCCCCCC=C
SMILES (Isomeric) CC(=O)OC(C=C)C#CC#CCC=CCCCCCC=C
InChI InChI=1S/C19H24O2/c1-4-6-7-8-9-10-11-12-13-14-15-16-17-19(5-2)21-18(3)20/h4-5,11-12,19H,1-2,6-10,13H2,3H3
InChI Key ROCQALVSCLHHIN-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C19H24O2
Molecular Weight 284.40 g/mol
Exact Mass 284.177630004 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 5.50
Atomic LogP (AlogP) 4.19
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 9

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Heptadeca-1,9,16-trien-4,6-diyn-3-yl acetate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9923 99.23%
Caco-2 - 0.6068 60.68%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Plasma membrane 0.5462 54.62%
OATP2B1 inhibitior - 0.8573 85.73%
OATP1B1 inhibitior + 0.8917 89.17%
OATP1B3 inhibitior + 0.9393 93.93%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.6976 69.76%
P-glycoprotein inhibitior - 0.7793 77.93%
P-glycoprotein substrate - 0.7930 79.30%
CYP3A4 substrate + 0.5744 57.44%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8651 86.51%
CYP3A4 inhibition - 0.8938 89.38%
CYP2C9 inhibition - 0.8048 80.48%
CYP2C19 inhibition - 0.8009 80.09%
CYP2D6 inhibition - 0.9568 95.68%
CYP1A2 inhibition - 0.5566 55.66%
CYP2C8 inhibition - 0.6519 65.19%
CYP inhibitory promiscuity - 0.6632 66.32%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5180 51.80%
Carcinogenicity (trinary) Non-required 0.5879 58.79%
Eye corrosion + 0.9710 97.10%
Eye irritation - 0.8596 85.96%
Skin irritation + 0.5709 57.09%
Skin corrosion - 0.9197 91.97%
Ames mutagenesis - 0.6900 69.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3871 38.71%
Micronuclear - 0.9500 95.00%
Hepatotoxicity - 0.5468 54.68%
skin sensitisation + 0.8849 88.49%
Respiratory toxicity - 0.7222 72.22%
Reproductive toxicity - 0.9556 95.56%
Mitochondrial toxicity - 0.9375 93.75%
Nephrotoxicity + 0.6827 68.27%
Acute Oral Toxicity (c) III 0.7321 73.21%
Estrogen receptor binding - 0.6409 64.09%
Androgen receptor binding - 0.5941 59.41%
Thyroid receptor binding + 0.5661 56.61%
Glucocorticoid receptor binding + 0.5539 55.39%
Aromatase binding - 0.6076 60.76%
PPAR gamma + 0.6608 66.08%
Honey bee toxicity - 0.7191 71.91%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity + 0.6062 60.62%
Fish aquatic toxicity + 0.9444 94.44%

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 95.67% 99.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 94.31% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.92% 96.09%
CHEMBL2581 P07339 Cathepsin D 91.58% 98.95%
CHEMBL3975 P09467 Fructose-1,6-bisphosphatase 90.95% 92.95%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 86.30% 97.21%
CHEMBL340 P08684 Cytochrome P450 3A4 85.02% 91.19%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 84.19% 96.95%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.86% 96.00%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 80.54% 94.33%

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.
Aldama incana
Syncretocarpus sericeus

Cross-Links

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PubChem 162930734
LOTUS LTS0189125
wikiData Q105242097