Sodium icosa-5,8,11,14,17-pentaenoate

Details

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Internal ID 2cfa97d8-c168-41f1-a0b6-238e635a2f5d
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acids and conjugates > Long-chain fatty acids
IUPAC Name sodium;icosa-5,8,11,14,17-pentaenoate
SMILES (Canonical) CCC=CCC=CCC=CCC=CCC=CCCCC(=O)[O-].[Na+]
SMILES (Isomeric) CCC=CCC=CCC=CCC=CCC=CCCCC(=O)[O-].[Na+]
InChI InChI=1S/C20H30O2.Na/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20(21)22;/h3-4,6-7,9-10,12-13,15-16H,2,5,8,11,14,17-19H2,1H3,(H,21,22);/q;+1/p-1
InChI Key RBZYGQJEMWGTOH-UHFFFAOYSA-M
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H29NaO2
Molecular Weight 324.40 g/mol
Exact Mass 324.20652445 g/mol
Topological Polar Surface Area (TPSA) 40.10 Ų
XlogP 0.00
Atomic LogP (AlogP) 1.66
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 13

Synonyms

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DTXSID10993898
sodium icosa-5,8,11,14,17-pentaenoate
FT-0777896

2D Structure

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2D Structure of Sodium icosa-5,8,11,14,17-pentaenoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9802 98.02%
Caco-2 - 0.5205 52.05%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Plasma membrane 0.7752 77.52%
OATP2B1 inhibitior - 0.8545 85.45%
OATP1B1 inhibitior - 0.4036 40.36%
OATP1B3 inhibitior + 0.8968 89.68%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.6958 69.58%
P-glycoprotein inhibitior - 0.7084 70.84%
P-glycoprotein substrate - 0.9447 94.47%
CYP3A4 substrate - 0.6190 61.90%
CYP2C9 substrate - 0.5806 58.06%
CYP2D6 substrate - 0.8827 88.27%
CYP3A4 inhibition - 0.9561 95.61%
CYP2C9 inhibition - 0.8630 86.30%
CYP2C19 inhibition - 0.9158 91.58%
CYP2D6 inhibition - 0.9385 93.85%
CYP1A2 inhibition - 0.5177 51.77%
CYP2C8 inhibition - 0.9270 92.70%
CYP inhibitory promiscuity - 0.8689 86.89%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5820 58.20%
Carcinogenicity (trinary) Non-required 0.6279 62.79%
Eye corrosion + 0.8289 82.89%
Eye irritation - 0.6484 64.84%
Skin irritation + 0.5243 52.43%
Skin corrosion - 0.9401 94.01%
Ames mutagenesis - 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3719 37.19%
Micronuclear - 0.9400 94.00%
Hepatotoxicity - 0.7750 77.50%
skin sensitisation - 0.5688 56.88%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity - 0.8248 82.48%
Mitochondrial toxicity - 0.8625 86.25%
Nephrotoxicity - 0.7380 73.80%
Acute Oral Toxicity (c) III 0.7086 70.86%
Estrogen receptor binding + 0.7764 77.64%
Androgen receptor binding - 0.9374 93.74%
Thyroid receptor binding + 0.5175 51.75%
Glucocorticoid receptor binding + 0.6839 68.39%
Aromatase binding - 0.5126 51.26%
PPAR gamma + 0.8708 87.08%
Honey bee toxicity - 0.9808 98.08%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.6500 65.00%
Fish aquatic toxicity + 0.8845 88.45%

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 94.14% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.10% 96.09%
CHEMBL2581 P07339 Cathepsin D 89.59% 98.95%
CHEMBL1781 P11387 DNA topoisomerase I 82.61% 97.00%
CHEMBL239 Q07869 Peroxisome proliferator-activated receptor alpha 81.19% 90.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.09% 86.33%

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.
Citrus × aurantium
Citrus deliciosa

Cross-Links

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PubChem 44134688
NPASS NPC138440