9-Hydroxyoctadeca-2,4-dienoic acid

Details

Top
Internal ID 2b5a4eb4-4889-4cda-a485-edaf9feae92f
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Lineolic acids and derivatives
IUPAC Name 9-hydroxyoctadeca-2,4-dienoic acid
SMILES (Canonical) CCCCCCCCCC(CCCC=CC=CC(=O)O)O
SMILES (Isomeric) CCCCCCCCCC(CCCC=CC=CC(=O)O)O
InChI InChI=1S/C18H32O3/c1-2-3-4-5-6-8-11-14-17(19)15-12-9-7-10-13-16-18(20)21/h7,10,13,16-17,19H,2-6,8-9,11-12,14-15H2,1H3,(H,20,21)
InChI Key CUHJQOVOXFVMSQ-UHFFFAOYSA-N
Popularity 27 references in papers

Physical and Chemical Properties

Top
Molecular Formula C18H32O3
Molecular Weight 296.40 g/mol
Exact Mass 296.23514488 g/mol
Topological Polar Surface Area (TPSA) 57.50 Ų
XlogP 5.70
Atomic LogP (AlogP) 4.86
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 14

Synonyms

Top
74391-67-6
9-hydroxy-octadecadieneoic acid
DTXSID80706331

2D Structure

Top
2D Structure of 9-Hydroxyoctadeca-2,4-dienoic acid

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9874 98.74%
Caco-2 + 0.5354 53.54%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Mitochondria 0.6237 62.37%
OATP2B1 inhibitior - 0.8523 85.23%
OATP1B1 inhibitior + 0.9014 90.14%
OATP1B3 inhibitior + 0.8328 83.28%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.6376 63.76%
P-glycoprotein inhibitior - 0.9059 90.59%
P-glycoprotein substrate - 0.8275 82.75%
CYP3A4 substrate - 0.5589 55.89%
CYP2C9 substrate - 0.5995 59.95%
CYP2D6 substrate - 0.8951 89.51%
CYP3A4 inhibition - 0.9015 90.15%
CYP2C9 inhibition - 0.9132 91.32%
CYP2C19 inhibition - 0.9359 93.59%
CYP2D6 inhibition - 0.9424 94.24%
CYP1A2 inhibition + 0.7040 70.40%
CYP2C8 inhibition - 0.9103 91.03%
CYP inhibitory promiscuity - 0.8944 89.44%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.7735 77.35%
Carcinogenicity (trinary) Non-required 0.7187 71.87%
Eye corrosion + 0.5094 50.94%
Eye irritation - 0.6602 66.02%
Skin irritation + 0.5342 53.42%
Skin corrosion - 0.6600 66.00%
Ames mutagenesis - 0.9000 90.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7158 71.58%
Micronuclear - 0.9800 98.00%
Hepatotoxicity - 0.6698 66.98%
skin sensitisation + 0.5799 57.99%
Respiratory toxicity - 0.8000 80.00%
Reproductive toxicity - 0.8217 82.17%
Mitochondrial toxicity + 0.5250 52.50%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) IV 0.6309 63.09%
Estrogen receptor binding + 0.6083 60.83%
Androgen receptor binding - 0.6594 65.94%
Thyroid receptor binding + 0.6673 66.73%
Glucocorticoid receptor binding + 0.5411 54.11%
Aromatase binding - 0.6532 65.32%
PPAR gamma + 0.8997 89.97%
Honey bee toxicity - 0.9830 98.30%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity + 0.6900 69.00%
Fish aquatic toxicity + 0.9570 95.70%

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 95.24% 99.17%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 94.88% 97.29%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 92.44% 92.08%
CHEMBL2581 P07339 Cathepsin D 92.17% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.17% 96.09%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 90.63% 92.86%
CHEMBL3359 P21462 Formyl peptide receptor 1 88.65% 93.56%
CHEMBL230 P35354 Cyclooxygenase-2 88.25% 89.63%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 85.11% 100.00%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 84.86% 96.95%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 83.49% 100.00%
CHEMBL2001 Q9H244 Purinergic receptor P2Y12 83.46% 96.00%
CHEMBL4227 P25090 Lipoxin A4 receptor 82.82% 100.00%
CHEMBL221 P23219 Cyclooxygenase-1 82.58% 90.17%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 81.87% 85.94%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 80.57% 91.81%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 80.54% 96.47%

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.
Taraxacum platycarpum

Cross-Links

Top
PubChem 53740616
LOTUS LTS0253415
wikiData Q82639662