3E,9Z,12Z,15Z-octadecatetraenoic acid

Details

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Internal ID 11ba83ff-8653-427a-a352-0b27fa33d3f5
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Lineolic acids and derivatives
IUPAC Name (3E,9Z,12Z,15Z)-octadeca-3,9,12,15-tetraenoic acid
SMILES (Canonical) CCC=CCC=CCC=CCCCCC=CCC(=O)O
SMILES (Isomeric) CC/C=C\C/C=C\C/C=C\CCCC/C=C/CC(=O)O
InChI InChI=1S/C18H28O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18(19)20/h3-4,6-7,9-10,15-16H,2,5,8,11-14,17H2,1H3,(H,19,20)/b4-3-,7-6-,10-9-,16-15+
InChI Key JNIPNHCEUZIVID-BPJKAVOUSA-N
Popularity 1 reference 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) 37.30 Ų
XlogP 5.40
Atomic LogP (AlogP) 5.44
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 12

Synonyms

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C18:4n-3,6,9,15
trans-3, cis-9, cis-12, cis-15-octadecatetraenoic acid
LMFA01030167
SCHEMBL6112767

2D Structure

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2D Structure of 3E,9Z,12Z,15Z-octadecatetraenoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9943 99.43%
Caco-2 + 0.5877 58.77%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Plasma membrane 0.6946 69.46%
OATP2B1 inhibitior - 0.8578 85.78%
OATP1B1 inhibitior - 0.3923 39.23%
OATP1B3 inhibitior + 0.8013 80.13%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.5526 55.26%
P-glycoprotein inhibitior - 0.7859 78.59%
P-glycoprotein substrate - 0.9620 96.20%
CYP3A4 substrate - 0.6620 66.20%
CYP2C9 substrate + 0.6276 62.76%
CYP2D6 substrate - 0.8766 87.66%
CYP3A4 inhibition - 0.9421 94.21%
CYP2C9 inhibition - 0.9301 93.01%
CYP2C19 inhibition - 0.9729 97.29%
CYP2D6 inhibition - 0.9648 96.48%
CYP1A2 inhibition - 0.5000 50.00%
CYP2C8 inhibition - 0.9356 93.56%
CYP inhibitory promiscuity - 0.9541 95.41%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6135 61.35%
Carcinogenicity (trinary) Non-required 0.6986 69.86%
Eye corrosion + 0.9757 97.57%
Eye irritation + 0.6653 66.53%
Skin irritation + 0.7978 79.78%
Skin corrosion - 0.7632 76.32%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4729 47.29%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.7000 70.00%
skin sensitisation + 0.8178 81.78%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity - 0.7476 74.76%
Mitochondrial toxicity - 0.6875 68.75%
Nephrotoxicity - 0.8190 81.90%
Acute Oral Toxicity (c) III 0.5032 50.32%
Estrogen receptor binding + 0.7164 71.64%
Androgen receptor binding - 0.8494 84.94%
Thyroid receptor binding + 0.5150 51.50%
Glucocorticoid receptor binding - 0.6818 68.18%
Aromatase binding + 0.5637 56.37%
PPAR gamma + 0.8414 84.14%
Honey bee toxicity - 0.9921 99.21%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.6600 66.00%
Fish aquatic toxicity + 0.7428 74.28%

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
CHEMBL2581 P07339 Cathepsin D 93.15% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.13% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.53% 99.17%
CHEMBL239 Q07869 Peroxisome proliferator-activated receptor alpha 87.74% 90.75%
CHEMBL221 P23219 Cyclooxygenase-1 87.68% 90.17%
CHEMBL1781 P11387 DNA topoisomerase I 84.53% 97.00%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.61% 96.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.22% 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.
Tecoma stans

Cross-Links

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PubChem 5282835
LOTUS LTS0109765
wikiData Q76286223