8,11,14-Octadecatrienoic acid

Details

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Internal ID eefbcd0a-f222-482c-98d9-f16b17774a73
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Lineolic acids and derivatives
IUPAC Name octadeca-8,11,14-trienoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C18H30O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18(19)20/h4-5,7-8,10-11H,2-3,6,9,12-17H2,1H3,(H,19,20)
InChI Key CTMZJQAVRYEWHS-UHFFFAOYSA-N
Popularity 9 references in papers

Physical and Chemical Properties

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Molecular Formula C18H30O2
Molecular Weight 278.40 g/mol
Exact Mass 278.224580195 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 5.90
Atomic LogP (AlogP) 5.66
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 13

Synonyms

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OCTDA
RefChem:914446
SCHEMBL26624923
OCTADECA-8,11,14-TRIENOIC ACID

2D Structure

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2D Structure of 8,11,14-Octadecatrienoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9930 99.30%
Caco-2 + 0.8050 80.50%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Plasma membrane 0.6593 65.93%
OATP2B1 inhibitior - 0.8523 85.23%
OATP1B1 inhibitior - 0.4925 49.25%
OATP1B3 inhibitior - 0.3398 33.98%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.5599 55.99%
P-glycoprotein inhibitior - 0.7677 76.77%
P-glycoprotein substrate - 0.9527 95.27%
CYP3A4 substrate - 0.6602 66.02%
CYP2C9 substrate + 0.6276 62.76%
CYP2D6 substrate - 0.8766 87.66%
CYP3A4 inhibition - 0.9420 94.20%
CYP2C9 inhibition - 0.8602 86.02%
CYP2C19 inhibition - 0.9434 94.34%
CYP2D6 inhibition - 0.9564 95.64%
CYP1A2 inhibition + 0.7917 79.17%
CYP2C8 inhibition - 0.9163 91.63%
CYP inhibitory promiscuity - 0.9438 94.38%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6535 65.35%
Carcinogenicity (trinary) Non-required 0.6276 62.76%
Eye corrosion + 0.9420 94.20%
Eye irritation + 0.7813 78.13%
Skin irritation + 0.8022 80.22%
Skin corrosion + 0.5538 55.38%
Ames mutagenesis - 0.9200 92.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3965 39.65%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.5500 55.00%
skin sensitisation + 0.8343 83.43%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity - 0.7582 75.82%
Mitochondrial toxicity + 0.6625 66.25%
Nephrotoxicity - 0.7941 79.41%
Acute Oral Toxicity (c) IV 0.5506 55.06%
Estrogen receptor binding - 0.5478 54.78%
Androgen receptor binding - 0.9196 91.96%
Thyroid receptor binding + 0.6878 68.78%
Glucocorticoid receptor binding - 0.5490 54.90%
Aromatase binding - 0.5574 55.74%
PPAR gamma + 0.8683 86.83%
Honey bee toxicity - 0.9932 99.32%
Biodegradation + 0.6750 67.50%
Crustacea aquatic toxicity + 0.5900 59.00%
Fish aquatic toxicity + 0.9045 90.45%

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 96.98% 99.17%
CHEMBL2581 P07339 Cathepsin D 95.16% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.69% 96.09%
CHEMBL1781 P11387 DNA topoisomerase I 91.51% 97.00%
CHEMBL221 P23219 Cyclooxygenase-1 90.73% 90.17%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 85.82% 92.08%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.60% 96.95%

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.
Hansenia forbesii
Hansenia weberbaueriana

Cross-Links

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PubChem 21015
NPASS NPC109093