2-Hydroxyethyl octadeca-9,12-dienoate

Details

Top
Internal ID 072a671e-f168-4d51-8ab2-b1b4b942fd79
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Lineolic acids and derivatives
IUPAC Name 2-hydroxyethyl octadeca-9,12-dienoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H36O3/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-20(22)23-19-18-21/h6-7,9-10,21H,2-5,8,11-19H2,1H3
InChI Key KKNRLFRQWDXUQD-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

Top
Molecular Formula C20H36O3
Molecular Weight 324.50 g/mol
Exact Mass 324.26644501 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 6.20
Atomic LogP (AlogP) 5.34
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 16

Synonyms

Top
61596-58-5

2D Structure

Top
2D Structure of 2-Hydroxyethyl octadeca-9,12-dienoate

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9855 98.55%
Caco-2 + 0.6042 60.42%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Mitochondria 0.5313 53.13%
OATP2B1 inhibitior - 0.8538 85.38%
OATP1B1 inhibitior - 0.4212 42.12%
OATP1B3 inhibitior + 0.8845 88.45%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.5636 56.36%
P-glycoprotein inhibitior - 0.7526 75.26%
P-glycoprotein substrate - 0.8878 88.78%
CYP3A4 substrate - 0.5172 51.72%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8707 87.07%
CYP3A4 inhibition - 0.9125 91.25%
CYP2C9 inhibition - 0.9251 92.51%
CYP2C19 inhibition - 0.9030 90.30%
CYP2D6 inhibition - 0.9371 93.71%
CYP1A2 inhibition - 0.7120 71.20%
CYP2C8 inhibition - 0.6936 69.36%
CYP inhibitory promiscuity - 0.9386 93.86%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.7200 72.00%
Carcinogenicity (trinary) Non-required 0.7229 72.29%
Eye corrosion + 0.8048 80.48%
Eye irritation + 0.7954 79.54%
Skin irritation + 0.6608 66.08%
Skin corrosion - 0.9169 91.69%
Ames mutagenesis - 0.8800 88.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5084 50.84%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.5623 56.23%
skin sensitisation - 0.7502 75.02%
Respiratory toxicity - 0.8444 84.44%
Reproductive toxicity - 0.8201 82.01%
Mitochondrial toxicity - 0.9500 95.00%
Nephrotoxicity - 0.6115 61.15%
Acute Oral Toxicity (c) III 0.7829 78.29%
Estrogen receptor binding + 0.6469 64.69%
Androgen receptor binding - 0.7967 79.67%
Thyroid receptor binding - 0.5406 54.06%
Glucocorticoid receptor binding - 0.5472 54.72%
Aromatase binding - 0.7638 76.38%
PPAR gamma + 0.6374 63.74%
Honey bee toxicity - 0.9826 98.26%
Biodegradation + 0.7750 77.50%
Crustacea aquatic toxicity + 0.7185 71.85%
Fish aquatic toxicity + 0.8705 87.05%

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 98.74% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.80% 96.09%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 94.89% 92.08%
CHEMBL2581 P07339 Cathepsin D 93.14% 98.95%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 92.36% 97.29%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 90.52% 85.94%
CHEMBL230 P35354 Cyclooxygenase-2 89.47% 89.63%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 86.96% 91.81%
CHEMBL2885 P07451 Carbonic anhydrase III 86.65% 87.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.03% 86.33%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 83.77% 92.86%
CHEMBL1781 P11387 DNA topoisomerase I 83.49% 97.00%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 82.98% 94.33%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.44% 91.11%
CHEMBL5255 O00206 Toll-like receptor 4 81.35% 92.50%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.25% 96.00%

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.
Tagetes erecta

Cross-Links

Top
PubChem 53999537
LOTUS LTS0187584
wikiData Q105142276