Methyl tetradeca-2,4,6,12-tetraen-8,10-diynoate

Details

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Internal ID 5e859b44-5ad3-4ad9-8628-273ca2a7c7b2
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acid esters
IUPAC Name methyl tetradeca-2,4,6,12-tetraen-8,10-diynoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H14O2/c1-3-4-5-6-7-8-9-10-11-12-13-14-15(16)17-2/h3-4,9-14H,1-2H3
InChI Key VTWQBDRIAQOYJJ-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H14O2
Molecular Weight 226.27 g/mol
Exact Mass 226.099379685 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 3.70
Atomic LogP (AlogP) 2.41
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Methyl tetradeca-2,4,6,12-tetraen-8,10-diynoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9936 99.36%
Caco-2 + 0.7002 70.02%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.6115 61.15%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9012 90.12%
OATP1B3 inhibitior + 0.9599 95.99%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.5932 59.32%
P-glycoprotein inhibitior - 0.9252 92.52%
P-glycoprotein substrate - 0.9338 93.38%
CYP3A4 substrate - 0.5279 52.79%
CYP2C9 substrate - 0.5981 59.81%
CYP2D6 substrate - 0.9002 90.02%
CYP3A4 inhibition - 0.9696 96.96%
CYP2C9 inhibition - 0.9195 91.95%
CYP2C19 inhibition - 0.9357 93.57%
CYP2D6 inhibition - 0.9695 96.95%
CYP1A2 inhibition - 0.7917 79.17%
CYP2C8 inhibition - 0.8896 88.96%
CYP inhibitory promiscuity - 0.8674 86.74%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.6747 67.47%
Carcinogenicity (trinary) Non-required 0.6387 63.87%
Eye corrosion + 0.9747 97.47%
Eye irritation + 0.7858 78.58%
Skin irritation + 0.8380 83.80%
Skin corrosion + 0.7137 71.37%
Ames mutagenesis - 0.5037 50.37%
Human Ether-a-go-go-Related Gene inhibition - 0.4507 45.07%
Micronuclear - 0.9200 92.00%
Hepatotoxicity - 0.5038 50.38%
skin sensitisation + 0.8692 86.92%
Respiratory toxicity - 0.6556 65.56%
Reproductive toxicity - 0.9556 95.56%
Mitochondrial toxicity - 0.9125 91.25%
Nephrotoxicity + 0.7943 79.43%
Acute Oral Toxicity (c) III 0.7606 76.06%
Estrogen receptor binding + 0.5603 56.03%
Androgen receptor binding - 0.6806 68.06%
Thyroid receptor binding + 0.5206 52.06%
Glucocorticoid receptor binding + 0.6810 68.10%
Aromatase binding + 0.7817 78.17%
PPAR gamma - 0.5713 57.13%
Honey bee toxicity - 0.7747 77.47%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity + 0.6763 67.63%

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
CHEMBL4040 P28482 MAP kinase ERK2 95.52% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.45% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.93% 94.45%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.25% 99.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 80.64% 91.11%

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.
Sanvitalia procumbens

Cross-Links

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PubChem 163075194
LOTUS LTS0014431
wikiData Q105293064