Methyl hexadeca-6,8,12,14-tetraen-10-ynoate

Details

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Internal ID b6a014e3-b8ff-4fd5-ba39-ea118619f7a3
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acid esters > Fatty acid methyl esters
IUPAC Name methyl hexadeca-6,8,12,14-tetraen-10-ynoate
SMILES (Canonical) CC=CC=CC#CC=CC=CCCCCC(=O)OC
SMILES (Isomeric) CC=CC=CC#CC=CC=CCCCCC(=O)OC
InChI InChI=1S/C17H22O2/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17(18)19-2/h3-6,9-12H,13-16H2,1-2H3
InChI Key NWFXMXAIHXHKDH-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C17H22O2
Molecular Weight 258.35 g/mol
Exact Mass 258.161979940 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 4.60
Atomic LogP (AlogP) 3.97
H-Bond Acceptor 2
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 Methyl hexadeca-6,8,12,14-tetraen-10-ynoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9910 99.10%
Caco-2 + 0.8040 80.40%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.4533 45.33%
OATP2B1 inhibitior - 0.8599 85.99%
OATP1B1 inhibitior + 0.8329 83.29%
OATP1B3 inhibitior + 0.9066 90.66%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.4747 47.47%
P-glycoprotein inhibitior - 0.8443 84.43%
P-glycoprotein substrate - 0.8720 87.20%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8720 87.20%
CYP3A4 inhibition - 0.9435 94.35%
CYP2C9 inhibition - 0.9327 93.27%
CYP2C19 inhibition - 0.9361 93.61%
CYP2D6 inhibition - 0.9594 95.94%
CYP1A2 inhibition - 0.6376 63.76%
CYP2C8 inhibition - 0.8241 82.41%
CYP inhibitory promiscuity - 0.8155 81.55%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5500 55.00%
Carcinogenicity (trinary) Non-required 0.6949 69.49%
Eye corrosion + 0.9248 92.48%
Eye irritation - 0.9076 90.76%
Skin irritation + 0.6826 68.26%
Skin corrosion - 0.9783 97.83%
Ames mutagenesis - 0.8600 86.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8150 81.50%
Micronuclear - 0.9700 97.00%
Hepatotoxicity - 0.6815 68.15%
skin sensitisation + 0.7908 79.08%
Respiratory toxicity - 0.6667 66.67%
Reproductive toxicity - 0.9286 92.86%
Mitochondrial toxicity - 0.9500 95.00%
Nephrotoxicity + 0.5309 53.09%
Acute Oral Toxicity (c) III 0.8880 88.80%
Estrogen receptor binding - 0.5118 51.18%
Androgen receptor binding - 0.7018 70.18%
Thyroid receptor binding + 0.6312 63.12%
Glucocorticoid receptor binding + 0.6101 61.01%
Aromatase binding + 0.5404 54.04%
PPAR gamma - 0.4876 48.76%
Honey bee toxicity - 0.8873 88.73%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity + 0.6900 69.00%
Fish aquatic toxicity + 0.8041 80.41%

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 96.29% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.93% 96.09%
CHEMBL4040 P28482 MAP kinase ERK2 93.38% 83.82%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.87% 91.11%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 87.32% 96.00%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 86.16% 94.33%
CHEMBL2581 P07339 Cathepsin D 84.29% 98.95%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.34% 96.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.01% 94.45%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 81.25% 89.34%

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.
Chrysocoma microphylla

Cross-Links

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PubChem 163007618
LOTUS LTS0033440
wikiData Q105186594