Methyl Dec-9-ynoate

Details

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Internal ID 51b1ccba-807f-45aa-a9d6-dd293a62f879
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acid esters > Fatty acid methyl esters
IUPAC Name methyl dec-9-ynoate
SMILES (Canonical) COC(=O)CCCCCCCC#C
SMILES (Isomeric) COC(=O)CCCCCCCC#C
InChI InChI=1S/C11H18O2/c1-3-4-5-6-7-8-9-10-11(12)13-2/h1H,4-10H2,2H3
InChI Key SXKMLYGXKLNTRS-UHFFFAOYSA-N
Popularity 10 references in papers

Physical and Chemical Properties

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Molecular Formula C11H18O2
Molecular Weight 182.26 g/mol
Exact Mass 182.130679813 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 3.10
Atomic LogP (AlogP) 2.52
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 7

Synonyms

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62285-66-9
9-Decynoic acid, methyl ester
dec-9-ynoic acid methyl ester
SCHEMBL2467407
DTXSID00453794
AT21757

2D Structure

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2D Structure of Methyl Dec-9-ynoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9917 99.17%
Caco-2 + 0.8266 82.66%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.5665 56.65%
OATP2B1 inhibitior - 0.8467 84.67%
OATP1B1 inhibitior + 0.9432 94.32%
OATP1B3 inhibitior + 0.9159 91.59%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.7796 77.96%
P-glycoprotein inhibitior - 0.9760 97.60%
P-glycoprotein substrate - 0.9418 94.18%
CYP3A4 substrate - 0.5803 58.03%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8394 83.94%
CYP3A4 inhibition - 0.9626 96.26%
CYP2C9 inhibition - 0.8888 88.88%
CYP2C19 inhibition - 0.9361 93.61%
CYP2D6 inhibition - 0.9644 96.44%
CYP1A2 inhibition - 0.5817 58.17%
CYP2C8 inhibition - 0.9198 91.98%
CYP inhibitory promiscuity - 0.9070 90.70%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5920 59.20%
Carcinogenicity (trinary) Non-required 0.7124 71.24%
Eye corrosion + 0.9790 97.90%
Eye irritation + 0.8151 81.51%
Skin irritation + 0.6104 61.04%
Skin corrosion - 0.9567 95.67%
Ames mutagenesis - 0.8800 88.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5874 58.74%
Micronuclear - 0.9700 97.00%
Hepatotoxicity - 0.7379 73.79%
skin sensitisation + 0.5163 51.63%
Respiratory toxicity - 0.8444 84.44%
Reproductive toxicity - 0.9103 91.03%
Mitochondrial toxicity - 0.9625 96.25%
Nephrotoxicity + 0.6187 61.87%
Acute Oral Toxicity (c) III 0.7735 77.35%
Estrogen receptor binding - 0.8790 87.90%
Androgen receptor binding - 0.9313 93.13%
Thyroid receptor binding - 0.7608 76.08%
Glucocorticoid receptor binding - 0.7894 78.94%
Aromatase binding - 0.7269 72.69%
PPAR gamma - 0.5087 50.87%
Honey bee toxicity - 0.9466 94.66%
Biodegradation + 0.7000 70.00%
Crustacea aquatic toxicity + 0.5624 56.24%
Fish aquatic toxicity + 0.7547 75.47%

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 96.49% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 94.13% 99.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.94% 91.11%
CHEMBL221 P23219 Cyclooxygenase-1 87.29% 90.17%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 86.54% 94.33%
CHEMBL2581 P07339 Cathepsin D 85.33% 98.95%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.54% 96.00%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 82.85% 95.17%

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.
Hibiscus rosa-sinensis

Cross-Links

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PubChem 11063054
LOTUS LTS0266164
wikiData Q82275039