13-Hydroxy-9,11,15-octadecatrienoic acid

Details

Top
Internal ID 3ca3a84a-3d40-4a29-81bd-a091fc4866be
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Lineolic acids and derivatives
IUPAC Name 13-hydroxyoctadeca-9,11,15-trienoic acid
SMILES (Canonical) CCC=CCC(C=CC=CCCCCCCCC(=O)O)O
SMILES (Isomeric) CCC=CCC(C=CC=CCCCCCCCC(=O)O)O
InChI InChI=1S/C18H30O3/c1-2-3-11-14-17(19)15-12-9-7-5-4-6-8-10-13-16-18(20)21/h3,7,9,11-12,15,17,19H,2,4-6,8,10,13-14,16H2,1H3,(H,20,21)
InChI Key KLLGGGQNRTVBSU-UHFFFAOYSA-N
Popularity 9 references in papers

Physical and Chemical Properties

Top
Molecular Formula C18H30O3
Molecular Weight 294.40 g/mol
Exact Mass 294.21949481 g/mol
Topological Polar Surface Area (TPSA) 57.50 Ų
XlogP 4.80
Atomic LogP (AlogP) 4.63
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 13

Synonyms

Top
13-hydroxy-9,11,15-octadecatrienoic acid

2D Structure

Top
2D Structure of 13-Hydroxy-9,11,15-octadecatrienoic acid

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9801 98.01%
Caco-2 - 0.5202 52.02%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.7429 74.29%
Subcellular localzation Mitochondria 0.7106 71.06%
OATP2B1 inhibitior - 0.8544 85.44%
OATP1B1 inhibitior + 0.8199 81.99%
OATP1B3 inhibitior + 0.8868 88.68%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.4731 47.31%
P-glycoprotein inhibitior - 0.7506 75.06%
P-glycoprotein substrate - 0.9014 90.14%
CYP3A4 substrate - 0.5623 56.23%
CYP2C9 substrate - 0.5905 59.05%
CYP2D6 substrate - 0.8674 86.74%
CYP3A4 inhibition - 0.9305 93.05%
CYP2C9 inhibition - 0.9122 91.22%
CYP2C19 inhibition - 0.9474 94.74%
CYP2D6 inhibition - 0.9546 95.46%
CYP1A2 inhibition - 0.6483 64.83%
CYP2C8 inhibition - 0.8803 88.03%
CYP inhibitory promiscuity - 0.9144 91.44%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.7635 76.35%
Carcinogenicity (trinary) Non-required 0.6666 66.66%
Eye corrosion + 0.5000 50.00%
Eye irritation - 0.7231 72.31%
Skin irritation - 0.5965 59.65%
Skin corrosion - 0.7641 76.41%
Ames mutagenesis - 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4700 47.00%
Micronuclear - 0.9700 97.00%
Hepatotoxicity - 0.6321 63.21%
skin sensitisation + 0.4909 49.09%
Respiratory toxicity + 0.7000 70.00%
Reproductive toxicity - 0.7228 72.28%
Mitochondrial toxicity + 0.6625 66.25%
Nephrotoxicity - 0.8944 89.44%
Acute Oral Toxicity (c) IV 0.6007 60.07%
Estrogen receptor binding + 0.6287 62.87%
Androgen receptor binding - 0.7055 70.55%
Thyroid receptor binding + 0.5416 54.16%
Glucocorticoid receptor binding - 0.6477 64.77%
Aromatase binding - 0.6311 63.11%
PPAR gamma + 0.8138 81.38%
Honey bee toxicity - 0.9585 95.85%
Biodegradation + 0.6000 60.00%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.7906 79.06%

Targets

Top

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 97.20% 99.17%
CHEMBL2581 P07339 Cathepsin D 95.95% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.92% 96.09%
CHEMBL5285 Q99683 Mitogen-activated protein kinase kinase kinase 5 88.06% 92.26%
CHEMBL1781 P11387 DNA topoisomerase I 87.78% 97.00%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 85.59% 97.29%
CHEMBL221 P23219 Cyclooxygenase-1 85.56% 90.17%
CHEMBL3359 P21462 Formyl peptide receptor 1 84.32% 93.56%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 82.88% 100.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.83% 96.00%
CHEMBL4227 P25090 Lipoxin A4 receptor 80.56% 100.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 80.47% 91.11%

Plants that contains it

Top
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.
Croton cortesianus
Morinda citrifolia
Potamogeton illinoensis

Cross-Links

Top
PubChem 53394276
LOTUS LTS0061896
wikiData Q105142674