Methyl icosa-5,7,9,14,17-pentaenoate

Details

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Internal ID c3d1aea0-cb64-4089-8387-2d99bd133f33
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acid esters > Fatty acid methyl esters
IUPAC Name methyl icosa-5,7,9,14,17-pentaenoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C21H32O2/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21(22)23-2/h4-5,7-8,12-17H,3,6,9-11,18-20H2,1-2H3
InChI Key KYCHHUXOABPSFL-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C21H32O2
Molecular Weight 316.50 g/mol
Exact Mass 316.240230259 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 6.20
Atomic LogP (AlogP) 6.08
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 13

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Methyl icosa-5,7,9,14,17-pentaenoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9962 99.62%
Caco-2 + 0.6472 64.72%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Plasma membrane 0.5877 58.77%
OATP2B1 inhibitior - 0.8567 85.67%
OATP1B1 inhibitior - 0.3427 34.27%
OATP1B3 inhibitior + 0.8879 88.79%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.8771 87.71%
P-glycoprotein inhibitior - 0.5374 53.74%
P-glycoprotein substrate - 0.8697 86.97%
CYP3A4 substrate - 0.5281 52.81%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8773 87.73%
CYP3A4 inhibition - 0.9738 97.38%
CYP2C9 inhibition - 0.9432 94.32%
CYP2C19 inhibition - 0.9521 95.21%
CYP2D6 inhibition - 0.9519 95.19%
CYP1A2 inhibition - 0.5574 55.74%
CYP2C8 inhibition - 0.7712 77.12%
CYP inhibitory promiscuity - 0.8346 83.46%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6000 60.00%
Carcinogenicity (trinary) Non-required 0.7586 75.86%
Eye corrosion + 0.9418 94.18%
Eye irritation - 0.7256 72.56%
Skin irritation + 0.5097 50.97%
Skin corrosion - 0.9951 99.51%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8050 80.50%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.7315 73.15%
skin sensitisation + 0.8003 80.03%
Respiratory toxicity - 0.6444 64.44%
Reproductive toxicity - 0.9778 97.78%
Mitochondrial toxicity - 0.9875 98.75%
Nephrotoxicity - 0.6611 66.11%
Acute Oral Toxicity (c) III 0.7281 72.81%
Estrogen receptor binding + 0.6851 68.51%
Androgen receptor binding - 0.8488 84.88%
Thyroid receptor binding + 0.5340 53.40%
Glucocorticoid receptor binding + 0.6637 66.37%
Aromatase binding - 0.6556 65.56%
PPAR gamma + 0.7022 70.22%
Honey bee toxicity - 0.9564 95.64%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity + 0.5700 57.00%
Fish aquatic toxicity + 0.9123 91.23%

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 96.10% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.55% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.69% 91.11%
CHEMBL2581 P07339 Cathepsin D 88.13% 98.95%
CHEMBL239 Q07869 Peroxisome proliferator-activated receptor alpha 88.06% 90.75%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 86.61% 94.33%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.86% 96.00%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.39% 96.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.00% 86.33%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 86020602
LOTUS LTS0209724
wikiData Q105147642