Methyl 17-acetyloxyheptadeca-7,9,15-trien-11,13-diynoate

Details

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Internal ID ec062184-1dee-40c9-9f2f-350f17d01288
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohol esters
IUPAC Name methyl 17-acetyloxyheptadeca-7,9,15-trien-11,13-diynoate
SMILES (Canonical) CC(=O)OCC=CC#CC#CC=CC=CCCCCCC(=O)OC
SMILES (Isomeric) CC(=O)OCC=CC#CC#CC=CC=CCCCCCC(=O)OC
InChI InChI=1S/C20H24O4/c1-19(21)24-18-16-14-12-10-8-6-4-3-5-7-9-11-13-15-17-20(22)23-2/h3-5,7,14,16H,9,11,13,15,17-18H2,1-2H3
InChI Key VOPPYPDHFHINPK-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H24O4
Molecular Weight 328.40 g/mol
Exact Mass 328.16745924 g/mol
Topological Polar Surface Area (TPSA) 52.60 Ų
XlogP 4.20
Atomic LogP (AlogP) 3.35
H-Bond Acceptor 4
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 Methyl 17-acetyloxyheptadeca-7,9,15-trien-11,13-diynoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9677 96.77%
Caco-2 - 0.5835 58.35%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability - 0.7143 71.43%
Subcellular localzation Mitochondria 0.8482 84.82%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8644 86.44%
OATP1B3 inhibitior + 0.9475 94.75%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.5692 56.92%
P-glycoprotein inhibitior - 0.5590 55.90%
P-glycoprotein substrate - 0.7586 75.86%
CYP3A4 substrate + 0.5738 57.38%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8720 87.20%
CYP3A4 inhibition - 0.8181 81.81%
CYP2C9 inhibition - 0.8968 89.68%
CYP2C19 inhibition - 0.9383 93.83%
CYP2D6 inhibition - 0.9404 94.04%
CYP1A2 inhibition - 0.8085 80.85%
CYP2C8 inhibition - 0.7323 73.23%
CYP inhibitory promiscuity - 0.8444 84.44%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6623 66.23%
Carcinogenicity (trinary) Non-required 0.8047 80.47%
Eye corrosion + 0.5087 50.87%
Eye irritation - 0.9281 92.81%
Skin irritation - 0.6864 68.64%
Skin corrosion - 0.9901 99.01%
Ames mutagenesis - 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7543 75.43%
Micronuclear - 0.9500 95.00%
Hepatotoxicity - 0.5683 56.83%
skin sensitisation - 0.7158 71.58%
Respiratory toxicity - 0.8222 82.22%
Reproductive toxicity - 0.9064 90.64%
Mitochondrial toxicity - 0.9625 96.25%
Nephrotoxicity + 0.7383 73.83%
Acute Oral Toxicity (c) III 0.6869 68.69%
Estrogen receptor binding + 0.6765 67.65%
Androgen receptor binding - 0.5967 59.67%
Thyroid receptor binding - 0.5307 53.07%
Glucocorticoid receptor binding - 0.5199 51.99%
Aromatase binding - 0.5000 50.00%
PPAR gamma - 0.5234 52.34%
Honey bee toxicity - 0.8357 83.57%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity + 0.7800 78.00%
Fish aquatic toxicity + 0.9643 96.43%

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 96.88% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.79% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.70% 91.11%
CHEMBL4040 P28482 MAP kinase ERK2 93.78% 83.82%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 89.54% 96.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.71% 94.45%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 84.63% 94.33%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 81.13% 96.95%

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.
Baccharis trinervis

Cross-Links

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PubChem 162898745
LOTUS LTS0167838
wikiData Q105290335