methyl (9Z,12Z,15Z)-octadeca-9,12,15-trien-6-ynoate

Details

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Internal ID 5790336f-58e9-4f09-bea1-1e838259e57a
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acid esters > Fatty acid methyl esters
IUPAC Name methyl (9Z,12Z,15Z)-octadeca-9,12,15-trien-6-ynoate
SMILES (Canonical) CCC=CCC=CCC=CCC#CCCCCC(=O)OC
SMILES (Isomeric) CC/C=C\C/C=C\C/C=C\CC#CCCCCC(=O)OC
InChI InChI=1S/C19H28O2/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19(20)21-2/h4-5,7-8,10-11H,3,6,9,12,15-18H2,1-2H3/b5-4-,8-7-,11-10-
InChI Key FEGFXBKBZCJHCW-YSTUJMKBSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C19H28O2
Molecular Weight 288.40 g/mol
Exact Mass 288.208930132 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 5.30
Atomic LogP (AlogP) 4.97
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 10

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of methyl (9Z,12Z,15Z)-octadeca-9,12,15-trien-6-ynoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9953 99.53%
Caco-2 + 0.7358 73.58%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Plasma membrane 0.5678 56.78%
OATP2B1 inhibitior - 0.8565 85.65%
OATP1B1 inhibitior + 0.7966 79.66%
OATP1B3 inhibitior + 0.8954 89.54%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.6218 62.18%
P-glycoprotein inhibitior - 0.6902 69.02%
P-glycoprotein substrate - 0.8303 83.03%
CYP3A4 substrate - 0.5218 52.18%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8690 86.90%
CYP3A4 inhibition - 0.9374 93.74%
CYP2C9 inhibition - 0.9056 90.56%
CYP2C19 inhibition - 0.9231 92.31%
CYP2D6 inhibition - 0.9474 94.74%
CYP1A2 inhibition + 0.5209 52.09%
CYP2C8 inhibition - 0.6338 63.38%
CYP inhibitory promiscuity - 0.7552 75.52%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5800 58.00%
Carcinogenicity (trinary) Non-required 0.7468 74.68%
Eye corrosion + 0.8927 89.27%
Eye irritation - 0.6786 67.86%
Skin irritation - 0.5193 51.93%
Skin corrosion - 0.9870 98.70%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6744 67.44%
Micronuclear - 0.9700 97.00%
Hepatotoxicity - 0.6565 65.65%
skin sensitisation + 0.8333 83.33%
Respiratory toxicity - 0.7556 75.56%
Reproductive toxicity - 0.9778 97.78%
Mitochondrial toxicity - 0.9750 97.50%
Nephrotoxicity - 0.5852 58.52%
Acute Oral Toxicity (c) III 0.8110 81.10%
Estrogen receptor binding - 0.5208 52.08%
Androgen receptor binding - 0.8635 86.35%
Thyroid receptor binding + 0.5868 58.68%
Glucocorticoid receptor binding - 0.5994 59.94%
Aromatase binding - 0.5405 54.05%
PPAR gamma + 0.5691 56.91%
Honey bee toxicity - 0.9428 94.28%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity + 0.9371 93.71%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.56% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 95.48% 99.17%
CHEMBL239 Q07869 Peroxisome proliferator-activated receptor alpha 92.56% 90.75%
CHEMBL2581 P07339 Cathepsin D 87.70% 98.95%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 85.98% 96.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.06% 86.33%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 84.48% 94.33%
CHEMBL221 P23219 Cyclooxygenase-1 84.20% 90.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 80.85% 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.
Riccia fluitans

Cross-Links

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PubChem 101514817
LOTUS LTS0041624
wikiData Q104993953