Methyl 11-phenyl-undecanoate

Details

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Internal ID 3219bc21-f72b-4f43-b08d-c6d87aeac24a
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acid esters > Fatty acid methyl esters
IUPAC Name methyl 11-phenylundecanoate
SMILES (Canonical) COC(=O)CCCCCCCCCCC1=CC=CC=C1
SMILES (Isomeric) COC(=O)CCCCCCCCCCC1=CC=CC=C1
InChI InChI=1S/C18H28O2/c1-20-18(19)16-12-7-5-3-2-4-6-9-13-17-14-10-8-11-15-17/h8,10-11,14-15H,2-7,9,12-13,16H2,1H3
InChI Key OEYUUCWCJJESQQ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C18H28O2
Molecular Weight 276.40 g/mol
Exact Mass 276.208930132 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 6.00
Atomic LogP (AlogP) 4.91
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 11

Synonyms

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SCHEMBL9764517
OEYUUCWCJJESQQ-UHFFFAOYSA-N

2D Structure

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2D Structure of Methyl 11-phenyl-undecanoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.7829 78.29%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.4942 49.42%
OATP2B1 inhibitior - 0.8583 85.83%
OATP1B1 inhibitior + 0.9125 91.25%
OATP1B3 inhibitior + 0.9298 92.98%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior + 0.8097 80.97%
P-glycoprotein inhibitior - 0.7160 71.60%
P-glycoprotein substrate - 0.8258 82.58%
CYP3A4 substrate - 0.5649 56.49%
CYP2C9 substrate - 0.8000 80.00%
CYP2D6 substrate - 0.7965 79.65%
CYP3A4 inhibition - 0.9716 97.16%
CYP2C9 inhibition - 0.9494 94.94%
CYP2C19 inhibition - 0.9205 92.05%
CYP2D6 inhibition - 0.9437 94.37%
CYP1A2 inhibition - 0.6566 65.66%
CYP2C8 inhibition - 0.6418 64.18%
CYP inhibitory promiscuity - 0.8864 88.64%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7151 71.51%
Carcinogenicity (trinary) Non-required 0.7013 70.13%
Eye corrosion + 0.7235 72.35%
Eye irritation + 0.8790 87.90%
Skin irritation + 0.5717 57.17%
Skin corrosion - 0.9922 99.22%
Ames mutagenesis - 0.8500 85.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8697 86.97%
Micronuclear - 0.9715 97.15%
Hepatotoxicity - 0.6216 62.16%
skin sensitisation - 0.6789 67.89%
Respiratory toxicity - 0.7667 76.67%
Reproductive toxicity - 0.7455 74.55%
Mitochondrial toxicity - 0.9625 96.25%
Nephrotoxicity - 0.6121 61.21%
Acute Oral Toxicity (c) III 0.8361 83.61%
Estrogen receptor binding + 0.5975 59.75%
Androgen receptor binding - 0.7570 75.70%
Thyroid receptor binding + 0.6455 64.55%
Glucocorticoid receptor binding - 0.5417 54.17%
Aromatase binding - 0.6181 61.81%
PPAR gamma + 0.6242 62.42%
Honey bee toxicity - 0.9671 96.71%
Biodegradation + 0.7500 75.00%
Crustacea aquatic toxicity + 0.5400 54.00%
Fish aquatic toxicity + 0.9409 94.09%

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 97.71% 96.09%
CHEMBL2581 P07339 Cathepsin D 96.84% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 94.33% 99.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.43% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.97% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 86.02% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.85% 95.56%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 84.73% 94.62%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 83.81% 95.50%
CHEMBL5028 O14672 ADAM10 82.87% 97.50%
CHEMBL221 P23219 Cyclooxygenase-1 80.81% 90.17%

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.
Trichilia claussenii

Cross-Links

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PubChem 10660115
LOTUS LTS0111623
wikiData Q105190698