Icos-2-enoic acid

Details

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Internal ID 7fdd3d9d-31b5-46b8-bb54-473613834a57
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acids and conjugates > Long-chain fatty acids
IUPAC Name icos-2-enoic acid
SMILES (Canonical) CCCCCCCCCCCCCCCCCC=CC(=O)O
SMILES (Isomeric) CCCCCCCCCCCCCCCCCC=CC(=O)O
InChI InChI=1S/C20H38O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20(21)22/h18-19H,2-17H2,1H3,(H,21,22)
InChI Key FIKTURVKRGQNQD-UHFFFAOYSA-N
Popularity 107 references in papers

Physical and Chemical Properties

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Molecular Formula C20H38O2
Molecular Weight 310.50 g/mol
Exact Mass 310.287180451 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 9.20
Atomic LogP (AlogP) 6.89
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 17

Synonyms

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.DELTA.2-cis Eicosenoic Acid
eicosaenoic acid
DTXSID00865318
FT-0619855

2D Structure

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2D Structure of Icos-2-enoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9922 99.22%
Caco-2 + 0.5860 58.60%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Plasma membrane 0.6894 68.94%
OATP2B1 inhibitior - 0.8537 85.37%
OATP1B1 inhibitior + 0.8602 86.02%
OATP1B3 inhibitior - 0.3061 30.61%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.7577 75.77%
P-glycoprotein inhibitior - 0.8517 85.17%
P-glycoprotein substrate - 0.9620 96.20%
CYP3A4 substrate - 0.6861 68.61%
CYP2C9 substrate + 0.6079 60.79%
CYP2D6 substrate - 0.9072 90.72%
CYP3A4 inhibition - 0.9608 96.08%
CYP2C9 inhibition - 0.8948 89.48%
CYP2C19 inhibition - 0.9459 94.59%
CYP2D6 inhibition - 0.9474 94.74%
CYP1A2 inhibition + 0.7152 71.52%
CYP2C8 inhibition - 0.9183 91.83%
CYP inhibitory promiscuity - 0.8882 88.82%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6535 65.35%
Carcinogenicity (trinary) Non-required 0.6623 66.23%
Eye corrosion + 0.9838 98.38%
Eye irritation + 0.9678 96.78%
Skin irritation + 0.8268 82.68%
Skin corrosion - 0.8329 83.29%
Ames mutagenesis - 0.9000 90.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6417 64.17%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.6196 61.96%
skin sensitisation + 0.9319 93.19%
Respiratory toxicity - 0.9444 94.44%
Reproductive toxicity - 0.6397 63.97%
Mitochondrial toxicity - 0.5875 58.75%
Nephrotoxicity + 0.4535 45.35%
Acute Oral Toxicity (c) III 0.8593 85.93%
Estrogen receptor binding - 0.5000 50.00%
Androgen receptor binding - 0.7689 76.89%
Thyroid receptor binding + 0.6296 62.96%
Glucocorticoid receptor binding - 0.7111 71.11%
Aromatase binding - 0.7394 73.94%
PPAR gamma + 0.8312 83.12%
Honey bee toxicity - 0.9952 99.52%
Biodegradation + 0.9000 90.00%
Crustacea aquatic toxicity + 0.8334 83.34%
Fish aquatic toxicity + 0.9857 98.57%

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 95.24% 99.17%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 91.99% 92.08%
CHEMBL221 P23219 Cyclooxygenase-1 91.64% 90.17%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 89.80% 97.29%
CHEMBL230 P35354 Cyclooxygenase-2 87.20% 89.63%
CHEMBL2581 P07339 Cathepsin D 86.27% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.94% 96.09%
CHEMBL1781 P11387 DNA topoisomerase I 85.13% 97.00%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 84.68% 96.95%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 82.02% 92.86%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 81.63% 100.00%
CHEMBL3359 P21462 Formyl peptide receptor 1 80.73% 93.56%

Cross-Links

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PubChem 3035221
NPASS NPC154932
LOTUS LTS0201199
wikiData Q104995750