13-Hydroxy-2,4,8-tetradecatrienoic acid

Details

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Internal ID 61c78fdb-7f06-48dc-acd5-497679cacb39
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acids and conjugates > Long-chain fatty acids
IUPAC Name 13-hydroxytetradeca-2,4,8-trienoic acid
SMILES (Canonical) CC(CCCC=CCCC=CC=CC(=O)O)O
SMILES (Isomeric) CC(CCCC=CCCC=CC=CC(=O)O)O
InChI InChI=1S/C14H22O3/c1-13(15)11-9-7-5-3-2-4-6-8-10-12-14(16)17/h3,5-6,8,10,12-13,15H,2,4,7,9,11H2,1H3,(H,16,17)
InChI Key UZOXUKLWMRPYCQ-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C14H22O3
Molecular Weight 238.32 g/mol
Exact Mass 238.15689456 g/mol
Topological Polar Surface Area (TPSA) 57.50 Ų
XlogP 2.80
Atomic LogP (AlogP) 3.07
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 9

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 13-Hydroxy-2,4,8-tetradecatrienoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9790 97.90%
Caco-2 + 0.7386 73.86%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.7249 72.49%
OATP2B1 inhibitior - 0.8591 85.91%
OATP1B1 inhibitior + 0.9074 90.74%
OATP1B3 inhibitior + 0.8733 87.33%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.7390 73.90%
P-glycoprotein inhibitior - 0.9520 95.20%
P-glycoprotein substrate - 0.8802 88.02%
CYP3A4 substrate - 0.5642 56.42%
CYP2C9 substrate - 0.5995 59.95%
CYP2D6 substrate - 0.8951 89.51%
CYP3A4 inhibition - 0.9421 94.21%
CYP2C9 inhibition - 0.9249 92.49%
CYP2C19 inhibition - 0.9569 95.69%
CYP2D6 inhibition - 0.9608 96.08%
CYP1A2 inhibition + 0.6077 60.77%
CYP2C8 inhibition - 0.9789 97.89%
CYP inhibitory promiscuity - 0.9415 94.15%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.7535 75.35%
Carcinogenicity (trinary) Non-required 0.7337 73.37%
Eye corrosion + 0.6149 61.49%
Eye irritation - 0.4797 47.97%
Skin irritation + 0.5681 56.81%
Skin corrosion - 0.7900 79.00%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6208 62.08%
Micronuclear - 0.9800 98.00%
Hepatotoxicity - 0.7000 70.00%
skin sensitisation + 0.5541 55.41%
Respiratory toxicity - 0.7333 73.33%
Reproductive toxicity - 0.7864 78.64%
Mitochondrial toxicity - 0.5500 55.00%
Nephrotoxicity - 0.6408 64.08%
Acute Oral Toxicity (c) III 0.5647 56.47%
Estrogen receptor binding - 0.6488 64.88%
Androgen receptor binding - 0.8046 80.46%
Thyroid receptor binding + 0.5743 57.43%
Glucocorticoid receptor binding + 0.5584 55.84%
Aromatase binding - 0.6833 68.33%
PPAR gamma + 0.7320 73.20%
Honey bee toxicity - 0.9662 96.62%
Biodegradation + 0.5500 55.00%
Crustacea aquatic toxicity - 0.7000 70.00%
Fish aquatic toxicity + 0.9315 93.15%

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 90.81% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.43% 96.09%
CHEMBL2581 P07339 Cathepsin D 87.36% 98.95%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 87.12% 96.47%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 86.53% 100.00%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 84.82% 97.29%
CHEMBL3145 P42338 PI3-kinase p110-beta subunit 84.10% 98.75%
CHEMBL3359 P21462 Formyl peptide receptor 1 82.84% 93.56%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.81% 96.00%
CHEMBL3401 O75469 Pregnane X receptor 80.01% 94.73%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 129681942
LOTUS LTS0187938
wikiData Q104199123